Review



a pchk1 s317 rabbit cell signaling tech  (Cell Signaling Technology Inc)


Bioz Verified Symbol Cell Signaling Technology Inc is a verified supplier
Bioz Manufacturer Symbol Cell Signaling Technology Inc manufactures this product  
  • Logo
  • About
  • News
  • Press Release
  • Team
  • Advisors
  • Partners
  • Contact
  • Bioz Stars
  • Bioz vStars
  • 96

    Structured Review

    Cell Signaling Technology Inc a pchk1 s317 rabbit cell signaling tech
    A Pchk1 S317 Rabbit Cell Signaling Tech, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 636 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser317)+Antibody/pm41914023-71-40-43
    Average 96 stars, based on 636 article reviews
    a pchk1 s317 rabbit cell signaling tech - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Recombinant:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023

    Polymer:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023

    Incubation:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023

    Staining:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023

    Microscopy:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023

    Western Blot:

    Article Title: ZEB1 loss increases glioma stem cell tumorigenicity and resistance to chemoradiation
    Article Snippet: Glioblastoma (GBM) is associated with short survival, largely due to GBM resistance to existing therapies.. Even after surgical resection, chemoradiation treatment only increases survival from 12 months to 15 months.1 Much of the research evaluating the mechanisms surrounding both chemotherapy and radiation resistance has focused on the identification of a subset of cancer stem cells within GBMs, i.e., the glioma stem cells (GSCs).2–5 The GSCs have long been thought to be responsible for conferring chemoand radioresistance resulting in disease progression and shortened survival in GBM patients.6–9 Given that chemotherapy in conjunction with radiation plays a large role in increasing survival,10 we looked for other potential targets that may play a role in both chemotherapy and radiation resistance in GSCs.. The identification of targetable markers in GSCs has a potential therapeutic role, as shown recently by Putthisen et al., who demonstrated that GSC-associated sialic acid–modified glycan with Maackia amurensis lectin II (MAL-II)– binding alpha2,3-sialylated glycan (MAL-SG) has a role

    Article Title: Targeting the ATR/CHK1 Axis with PARP Inhibition Results in Tumor Regression in BRCA-Mutant Ovarian Cancer Models
    Article Snippet: Slides were incubated with pCHK1 (CST, Cat# 2348) antibody at 1:1000 titer for 40 minutes.

    Article Title: Removal of uracil by uracil DNA glycosylase limits pemetrexed cytotoxicity: overriding the limit with methoxyamine to inhibit base excision repair
    Article Snippet: Sources of primary antibody were as follows: cleaved PARP (BD Pharmingen, San Jose, CA, USA), γ H2AX (Bethyl), pChk1, Chk1, pcdc2, cyclin B1, topo II α , topoisomerase I, Bax, and Bcl2 (Cell Signaling, Danvers, MA, USA), phospho-histone H3 (Upstate Biotechnologies, Billerica, MA, USA) and α -tubulin (Sigma-Aldrich).

    Article Title: Reactive Oxygen Species-independent Oxidation of Thioredoxin in Hypoxia
    Article Snippet: The antibodies used in our study were obtained from the following vendors: Trx, p21, and Chk1 antibodies were obtained from Santa Cruz Biotechnology (Santa Cruz, CA); RNR, MnSOD, and Chk2 antibodies were obtained from Millipore (Billerica, MA); poly(ADP-ribose) polymerase (PARP), p53, phospho-p53 (Ser-15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Biphasic response of checkpoint control proteins in hyperoxia: Exposure to lower levels of oxygen induces genome maintenance genes in experimental baboon BPD
    Article Snippet: Chk2 antibody was obtained from Millipore (Billerica, MA); poly-ADP ribose polymerase (PARP), p53, phospho-p53 (ser15), and pChk1 antibodies were obtained from Cell Signaling Technologies (Beverly, MA).

    Article Title: Phosphorylation of nuclear Tau is modulated by distinct cellular pathways
    Article Snippet: Primary antibodies, usually incubated for 1 h at 37 °C, were specific for human Tau (Tau13, Santa Cruz, sc-21796, used at 1 μg/mL), GFP (Proteintech Europe, 66002–1-Ig, 7 μg/mL), calnexin (kind gift of Prof. Maurizio Molinari, IRB, Bellinzona, Switzerland, diluted 1:1,000), α-tubulin (Abcam, ab1825, 0.5 μg/mL or Cell Signaling, DM1A, diluted 1:500), pS 129 -H2A.X (Santa Cruz, sc-517348, 0.5 μg/mL), pATM (Cell Signaling, S1981, diluted 1:500), pChk1 (Cell Signaling, S345, diluted 1:500), pChk2 (Cell Signaling, T68, diluted 1:500), pATR (Cell Signaling, S428, diluted 1:500).

    Article Title: Natural bioactive gallic acid shows potential anticancer effects by inhibiting the proliferation and invasiveness behavior in human embryonic carcinoma cells
    Article Snippet: Cell Signaling Technology, Inc. supplied: p27 Kip1 (cat. no. 3686), p-EGFR (cat. no. 3777), EGFR (cat. no. 4267), phosphorylated (p-)JAK2 (cat. no. 3776), JAK2 (cat. no. 3230), p-STAT5 (cat. no. 9351), pCHK1 (cat. no. 2348), p-CHK2 (cat. no. 2197), p-ATM (cat. no. 5883), p-Histone (cat. no. 9718) and p-BRCA1 (cat. no. 9009).

    Article Title: Replication stress and defective checkpoints make fallopian tube epithelial cells putative drivers of high-grade serous ovarian cancer.
    Article Snippet: REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies gH2AX Millipore Cat# 05-636; RRID: AB_309864 PAX8 Proteintech Cat# 10336; RRID: AB_2918972 CK8 TROMA-I -DSHB Cat# AB_531826; RRID: AB_531826 53BP1 Bethyl Labs Cat# A300-272A; RRID:AB_185520 53BP1 BioLegend Cat# 933002; RRID:AB_2820202 Foxj1 Millipore Sigma Cat# HPA005714; RRID:AB_1078902 Rad51 Santa Cruz Cat# SC-8349; RRID:AB_2253533 pRPA32 (S4/S8) Bethyl Labs Cat# A300-245A; RRID:AB_210547 pRPA32 (S33) Bethyl Labs Cat# A300-246A; RRID:AB_2180847 pCHK1 Cell signaling Cat# 2348S; RRID:AB_331212 CHK1 Cell signaling Cat# 2360S; RRID:AB_2080320 Lamin B1 Cell Signaling Cat# 12586; RRID:AB_2650517 GAPDH Santa Cruz Cat# SC-25778; RRID:AB_10167668 Mouse Brca1 Dr. David Livingston In this paper P16 Santa Cruz Cat# SC-1661; RRID:AB_628067 Ki67 Novusbio Cat# NB500-170; RRID:AB_10001977 pH3(S28) BD Biosciences Cat# 558217; RRID:AB_397065 Anti-BrdU BD Pharmingen Cat# 556028; RRID:AB_396304 Rat anti-CldU Abcam Cat# Ab6326; RRID:AB_305426 Mouse anti-IdU BD Biosciences Cat# 555627; RRID:AB_395993 Alexa Fluor 555 goat anti-rat Invitrogen Cat# A21434; RRID:AB_2535855 Alexa Fluor 488 goat anti-mouse Invitrogen Cat# A10684; RRID:AB_2534064 Biological samples Human Ovarian surface epithelial and Fallopian tube epithelial tissue This Paper Brigham and Women’s Hospital (BWH) Chemicals, peptides, and recombinant proteins Citrate buffer pH 6 Millipore-Sigma Cat# C9999 Cisplatin Millipore-Sigma Cat# 232120 Hydroxyurea Millipore-Sigma Cat# H8627-1G Corning Matrigel Fisher scientific Cat# CB-40234A Propidium Iodide BD Pharmingen Cat# 550825 Critical commercial assays Novolink polymer detection kit Leica Cat# RE71401-CE CellTitter-Glo reagent Promega Cat# G7572 Experimental models: Cell lines M412, M56, M338, M4 In this paper N/A CD-1 (Endsley et al. , 2015)71 Dr. Joanna Burdette’s Lab IHOSE1431 (Shin et al. , 2018)47 Dr. Jae-hoon Kim’s Lab HOSE (F et al. , 2007)46 Dr. Frances Balkwill’s Lab FTE237 (Karst and Drapkin, 2012)48 Dr. Ronny Drapkin’s Lab FTE194 (Perets et al. , 2013)30 Dr. Ronny Drapkin’s Lab IHOSE1431ht In this paper (hTERT immortalized) N/A (Continued on next page) 18 Cell Reports 42, 113144, October 31, 2023



    Similar Products

    96
    Cell Signaling Technology Inc a pchk1 s317 rabbit cell signaling tech
    A Pchk1 S317 Rabbit Cell Signaling Tech, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser317)+Antibody/pm41914023-71-40-43
    Average 96 stars, based on 1 article reviews
    a pchk1 s317 rabbit cell signaling tech - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    96
    Cell Signaling Technology Inc pchk1 ser345
    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. <t>pCHK1</t> and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.
    Pchk1 Ser345, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser345)+Antibody/bio_rxiv__64898__2026__03__22__666038-344-16-18
    Average 96 stars, based on 1 article reviews
    pchk1 ser345 - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    96
    Cell Signaling Technology Inc anti pchk1 s345 cell signaling 2341s
    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. <t>pCHK1</t> and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.
    Anti Pchk1 S345 Cell Signaling 2341s, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser345)+Antibody/pmc12615678-416-16-17
    Average 96 stars, based on 1 article reviews
    anti pchk1 s345 cell signaling 2341s - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    96
    Cell Signaling Technology Inc pchk1 s317
    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. <t>pCHK1</t> and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.
    Pchk1 S317, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser317)+Antibody/pm40940837-77-65-66
    Average 96 stars, based on 1 article reviews
    pchk1 s317 - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    93
    Bethyl 2348 wb pchk1 s296 cell signaling 2349 wb atr bethyl laboratories
    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. <t>pCHK1</t> and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.
    2348 Wb Pchk1 S296 Cell Signaling 2349 Wb Atr Bethyl Laboratories, supplied by Bethyl, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/ATR+Antibody/pmc12235512__gkaf626_supplemental_file-5-25-34
    Average 93 stars, based on 1 article reviews
    2348 wb pchk1 s296 cell signaling 2349 wb atr bethyl laboratories - by Bioz Stars, 2026-10
    93/100 stars
      Buy from Supplier

    96
    Santa Cruz Biotechnology chk1 santa cruz sc 8408 wb pchk1
    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. <t>pCHK1</t> and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.
    Chk1 Santa Cruz Sc 8408 Wb Pchk1, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 96/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Chk1+Antibody/pmc12235512__gkaf626_supplemental_file-5-16-17
    Average 96 stars, based on 1 article reviews
    chk1 santa cruz sc 8408 wb pchk1 - by Bioz Stars, 2026-10
    96/100 stars
      Buy from Supplier

    93
    Cell Signaling Technology Inc pchk1 s280
    A-C. Analysis of MYCN , ATR and survival correlations in publicly available primary NB data (n=364) , similar to . D. Representative Alk-F1178S KI/0/Th-MYCN tg/0 and Th-MYCN tg/0 tumors were examined for <t>pChk1</t> <t>S280,</t> S317 and S345. Scale bar indicates 250 µm and 50 µm (in inserts). E. Immunoblottning for phosphorylation of Chk1 on sites: S280, S317 and S345, as well as total and pAlk, pAtr, pErk1/2 and pAkt in three Alk-F1178S KI/0 / Th-MYCN tg/0 and three Th-MYCN tg/tg tumors. Tubulin was employed as loading control. F. Tumor volume response in Th-MYCN mice treated with a 14-day ALKi/ATRi combination (elimusertib + lorlatinib) or monotherapy regimes (elimusertib only, lorlatinib only or vehicle). Combination therapy: 3d elimusertib 25 mg/kg twice/day (orange), followed by 4d lorlatinib 10 mg/kg twice/day (green), followed by 3d elimusertib 25 mg/kg and lorlatinib 10 mg/kg twice/day (purple) and finally 4d lorlatinib 10 mg/kg twice/day (green) after which animals were released from treatment (arrow). Elimusertib 25 mg/kg as monotherapy was given twice per day during the corresponding days of elimusertib in the combination therapy. Lorlatinib 10 mg/kg as monotherapy, or vehicle control, was given twice per day continuously during the 14-day treatment period. Mean ± SD. *=(day 15 and 17 for two of the elimusertib monotreated animals). Unpaired t-test of tumor volume, at d7 between vehicle and lorlatinib treated Th-MYCN (tg/tg) tumor bearing mice, P= 0.019. G. Representativ e ultrasound images of tumor regression during combination treatment in . Yellow dotted lines denote tumor, pink dotted lines denote aorta and renal artery, kidney outlined with cerise dotted lines. H. Kaplan-Meier visualizing survival outcome in treated Th-MYCN mice starting (day 0) at treatment release. Teal colored curve, with a ∼65% probability of survival at 200 days, indicates the combined curves of hemizygote Th-MYCN (blue dashed line, 60% survival) and homozygote Th-MYCN (green dashed line, 75%) mice that received ALKi/ATRi combination treatment. Red colored curve represents Th-MYCN homozygote mice that received ATRi monotreatment with elimusertib. Log-rank (Mantel-Cox) test between homozygote Th-MYCN (green) that received combination treatment and homozygote Th-MYCN (red) that received elimusertib monotreatment, P= 0.0067. I) Graph displaying simple linear regression for 27 NB samples, duplicate cores, (including 2 ganglioneuroblastoma indicated in red) between ALK and pCHK1 S280 immunohistochemistry stainings. Sections were manually scored (0-5) by an unblinded investigator and the mean of each sample duplicate was used in the tests. Pearson r=0.5201, p=0.0054. J) Example of immunohistochemistry staining for anti-ALK and pCHK1 S280 for one of the duplicate cores among the 27 investigated samples. Scored ALK=5, pCHK1 S280=4. Scale bar indicate 500 µm.
    Pchk1 S280, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser280)+Antibody/bio_rxiv__2025__07__17__665300-123-14-21
    Average 93 stars, based on 1 article reviews
    pchk1 s280 - by Bioz Stars, 2026-10
    93/100 stars
      Buy from Supplier

    93
    Cell Signaling Technology Inc anti pchk1
    A-C. Analysis of MYCN , ATR and survival correlations in publicly available primary NB data (n=364) , similar to . D. Representative Alk-F1178S KI/0/Th-MYCN tg/0 and Th-MYCN tg/0 tumors were examined for <t>pChk1</t> <t>S280,</t> S317 and S345. Scale bar indicates 250 µm and 50 µm (in inserts). E. Immunoblottning for phosphorylation of Chk1 on sites: S280, S317 and S345, as well as total and pAlk, pAtr, pErk1/2 and pAkt in three Alk-F1178S KI/0 / Th-MYCN tg/0 and three Th-MYCN tg/tg tumors. Tubulin was employed as loading control. F. Tumor volume response in Th-MYCN mice treated with a 14-day ALKi/ATRi combination (elimusertib + lorlatinib) or monotherapy regimes (elimusertib only, lorlatinib only or vehicle). Combination therapy: 3d elimusertib 25 mg/kg twice/day (orange), followed by 4d lorlatinib 10 mg/kg twice/day (green), followed by 3d elimusertib 25 mg/kg and lorlatinib 10 mg/kg twice/day (purple) and finally 4d lorlatinib 10 mg/kg twice/day (green) after which animals were released from treatment (arrow). Elimusertib 25 mg/kg as monotherapy was given twice per day during the corresponding days of elimusertib in the combination therapy. Lorlatinib 10 mg/kg as monotherapy, or vehicle control, was given twice per day continuously during the 14-day treatment period. Mean ± SD. *=(day 15 and 17 for two of the elimusertib monotreated animals). Unpaired t-test of tumor volume, at d7 between vehicle and lorlatinib treated Th-MYCN (tg/tg) tumor bearing mice, P= 0.019. G. Representativ e ultrasound images of tumor regression during combination treatment in . Yellow dotted lines denote tumor, pink dotted lines denote aorta and renal artery, kidney outlined with cerise dotted lines. H. Kaplan-Meier visualizing survival outcome in treated Th-MYCN mice starting (day 0) at treatment release. Teal colored curve, with a ∼65% probability of survival at 200 days, indicates the combined curves of hemizygote Th-MYCN (blue dashed line, 60% survival) and homozygote Th-MYCN (green dashed line, 75%) mice that received ALKi/ATRi combination treatment. Red colored curve represents Th-MYCN homozygote mice that received ATRi monotreatment with elimusertib. Log-rank (Mantel-Cox) test between homozygote Th-MYCN (green) that received combination treatment and homozygote Th-MYCN (red) that received elimusertib monotreatment, P= 0.0067. I) Graph displaying simple linear regression for 27 NB samples, duplicate cores, (including 2 ganglioneuroblastoma indicated in red) between ALK and pCHK1 S280 immunohistochemistry stainings. Sections were manually scored (0-5) by an unblinded investigator and the mean of each sample duplicate was used in the tests. Pearson r=0.5201, p=0.0054. J) Example of immunohistochemistry staining for anti-ALK and pCHK1 S280 for one of the duplicate cores among the 27 investigated samples. Scored ALK=5, pCHK1 S280=4. Scale bar indicate 500 µm.
    Anti Pchk1, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk1+antibody/Phospho-Chk1+(Ser280)+Antibody/bio_rxiv__2025__07__17__665300-131-25-28
    Average 93 stars, based on 1 article reviews
    anti pchk1 - by Bioz Stars, 2026-10
    93/100 stars
      Buy from Supplier

    Image Search Results


    a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. pCHK1 and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.

    Journal: bioRxiv

    Article Title: Strand-independent degradation of uncoupled forks by EXO1 activates ATR and restrains synthesis

    doi: 10.64898/2026.03.22.666038

    Figure Lengend Snippet: a., Plasmid DNA was replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield supercoiled (SC) products. Plasmid DNA harboring a LacR array was also replicated in Xenopus egg extracts in the presence of [α- 32 dATP] to yield either (1) θ structures when forks were localized to the LacR barrier, and θ* structures after adding in aphidicolin and IPTG to simultaneously to induce uncoupling or (2) DNA breaks when replicated in the presence of aphidicolin or etoposide. b., Samples from a were separated on an agarose gel and visualized by autoradiography. c., Replication was performed as in a, but in the absence of [α- 32 dATP], see Supplemental Fig 5a. pCHK1 and MCM10 proteins were detected by western blotting. d., Quantification of pCHK1 signal from c. Mean ± s.d. n=3. e., Plasmid DNA was replicated in Xenopus egg extracts. Forks were localized to the LacR barrier and uncoupling was induced by simultaneous addition of aphidicolin and IPTG. f., pCHK1 proteins from e were detected by western blotting. g., Quantification of pCHK1 signal from f. Mean ± s.d. n=3.

    Article Snippet: Primary antibodies used for western blotting were: EXO1, RAD51, MCM10 that has been previously described[ ], pCHK1 (Ser345) (Cell Signaling Technology 2341), and pATM (S1981) (Abcam ab36810).

    Techniques: Plasmid Preparation, Agarose Gel Electrophoresis, Autoradiography, Western Blot

    A-C. Analysis of MYCN , ATR and survival correlations in publicly available primary NB data (n=364) , similar to . D. Representative Alk-F1178S KI/0/Th-MYCN tg/0 and Th-MYCN tg/0 tumors were examined for pChk1 S280, S317 and S345. Scale bar indicates 250 µm and 50 µm (in inserts). E. Immunoblottning for phosphorylation of Chk1 on sites: S280, S317 and S345, as well as total and pAlk, pAtr, pErk1/2 and pAkt in three Alk-F1178S KI/0 / Th-MYCN tg/0 and three Th-MYCN tg/tg tumors. Tubulin was employed as loading control. F. Tumor volume response in Th-MYCN mice treated with a 14-day ALKi/ATRi combination (elimusertib + lorlatinib) or monotherapy regimes (elimusertib only, lorlatinib only or vehicle). Combination therapy: 3d elimusertib 25 mg/kg twice/day (orange), followed by 4d lorlatinib 10 mg/kg twice/day (green), followed by 3d elimusertib 25 mg/kg and lorlatinib 10 mg/kg twice/day (purple) and finally 4d lorlatinib 10 mg/kg twice/day (green) after which animals were released from treatment (arrow). Elimusertib 25 mg/kg as monotherapy was given twice per day during the corresponding days of elimusertib in the combination therapy. Lorlatinib 10 mg/kg as monotherapy, or vehicle control, was given twice per day continuously during the 14-day treatment period. Mean ± SD. *=(day 15 and 17 for two of the elimusertib monotreated animals). Unpaired t-test of tumor volume, at d7 between vehicle and lorlatinib treated Th-MYCN (tg/tg) tumor bearing mice, P= 0.019. G. Representativ e ultrasound images of tumor regression during combination treatment in . Yellow dotted lines denote tumor, pink dotted lines denote aorta and renal artery, kidney outlined with cerise dotted lines. H. Kaplan-Meier visualizing survival outcome in treated Th-MYCN mice starting (day 0) at treatment release. Teal colored curve, with a ∼65% probability of survival at 200 days, indicates the combined curves of hemizygote Th-MYCN (blue dashed line, 60% survival) and homozygote Th-MYCN (green dashed line, 75%) mice that received ALKi/ATRi combination treatment. Red colored curve represents Th-MYCN homozygote mice that received ATRi monotreatment with elimusertib. Log-rank (Mantel-Cox) test between homozygote Th-MYCN (green) that received combination treatment and homozygote Th-MYCN (red) that received elimusertib monotreatment, P= 0.0067. I) Graph displaying simple linear regression for 27 NB samples, duplicate cores, (including 2 ganglioneuroblastoma indicated in red) between ALK and pCHK1 S280 immunohistochemistry stainings. Sections were manually scored (0-5) by an unblinded investigator and the mean of each sample duplicate was used in the tests. Pearson r=0.5201, p=0.0054. J) Example of immunohistochemistry staining for anti-ALK and pCHK1 S280 for one of the duplicate cores among the 27 investigated samples. Scored ALK=5, pCHK1 S280=4. Scale bar indicate 500 µm.

    Journal: bioRxiv

    Article Title: ALK/ATR combination therapy is effective in neuroblastoma mouse tumors driven by MYCN

    doi: 10.1101/2025.07.17.665300

    Figure Lengend Snippet: A-C. Analysis of MYCN , ATR and survival correlations in publicly available primary NB data (n=364) , similar to . D. Representative Alk-F1178S KI/0/Th-MYCN tg/0 and Th-MYCN tg/0 tumors were examined for pChk1 S280, S317 and S345. Scale bar indicates 250 µm and 50 µm (in inserts). E. Immunoblottning for phosphorylation of Chk1 on sites: S280, S317 and S345, as well as total and pAlk, pAtr, pErk1/2 and pAkt in three Alk-F1178S KI/0 / Th-MYCN tg/0 and three Th-MYCN tg/tg tumors. Tubulin was employed as loading control. F. Tumor volume response in Th-MYCN mice treated with a 14-day ALKi/ATRi combination (elimusertib + lorlatinib) or monotherapy regimes (elimusertib only, lorlatinib only or vehicle). Combination therapy: 3d elimusertib 25 mg/kg twice/day (orange), followed by 4d lorlatinib 10 mg/kg twice/day (green), followed by 3d elimusertib 25 mg/kg and lorlatinib 10 mg/kg twice/day (purple) and finally 4d lorlatinib 10 mg/kg twice/day (green) after which animals were released from treatment (arrow). Elimusertib 25 mg/kg as monotherapy was given twice per day during the corresponding days of elimusertib in the combination therapy. Lorlatinib 10 mg/kg as monotherapy, or vehicle control, was given twice per day continuously during the 14-day treatment period. Mean ± SD. *=(day 15 and 17 for two of the elimusertib monotreated animals). Unpaired t-test of tumor volume, at d7 between vehicle and lorlatinib treated Th-MYCN (tg/tg) tumor bearing mice, P= 0.019. G. Representativ e ultrasound images of tumor regression during combination treatment in . Yellow dotted lines denote tumor, pink dotted lines denote aorta and renal artery, kidney outlined with cerise dotted lines. H. Kaplan-Meier visualizing survival outcome in treated Th-MYCN mice starting (day 0) at treatment release. Teal colored curve, with a ∼65% probability of survival at 200 days, indicates the combined curves of hemizygote Th-MYCN (blue dashed line, 60% survival) and homozygote Th-MYCN (green dashed line, 75%) mice that received ALKi/ATRi combination treatment. Red colored curve represents Th-MYCN homozygote mice that received ATRi monotreatment with elimusertib. Log-rank (Mantel-Cox) test between homozygote Th-MYCN (green) that received combination treatment and homozygote Th-MYCN (red) that received elimusertib monotreatment, P= 0.0067. I) Graph displaying simple linear regression for 27 NB samples, duplicate cores, (including 2 ganglioneuroblastoma indicated in red) between ALK and pCHK1 S280 immunohistochemistry stainings. Sections were manually scored (0-5) by an unblinded investigator and the mean of each sample duplicate was used in the tests. Pearson r=0.5201, p=0.0054. J) Example of immunohistochemistry staining for anti-ALK and pCHK1 S280 for one of the duplicate cores among the 27 investigated samples. Scored ALK=5, pCHK1 S280=4. Scale bar indicate 500 µm.

    Article Snippet: Primary antibodies against CHK1 (#2360, 1:200), pCHK1 S345 (#2348, 1:100), pCHK1 S317 (#12302, 1:1000), pCHK1 S280 (#2347, 1:50) were obtained from Cell Signaling Technology and diluted in in Signalstain antibody diluent (#8112S, Cell Signaling Technology) and incubated in 4°C overnight.

    Techniques: Phospho-proteomics, Control, Immunohistochemistry, Staining