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pchk2 thr68  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc pchk2 thr68
    Pchk2 Thr68, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 545 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/pchk2+thr68/Phospho-Chk2+(Thr68)+Rabbit+mAb/pm41535339-280-64-66
    Average 96 stars, based on 545 article reviews
    pchk2 thr68 - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Cell-Signaling:

    Article Title: CRAMP1-dependent histone H1 biogenesis is essential for topoisomerase II inhibitor tolerance
    Article Snippet: pCHK1 (Ser345) , Cell Signaling , (Cell Signaling Technology Cat# 2348, RRID: AB_331212 ). .. pCHK2 (Thr68) , Cell Signaling , (Cell Signaling Technology Cat# 2661, RRID: AB_331479 ). .. pKAP1 (Ser824) , Thermo Fisher Scientific , (Thermo Fisher Scientific Cat# A300-767A, RRID: AB_669740 ).

    Incubation:

    Article Title: Imidazolonylquinoline compounds and therapeutic uses thereof
    Article Snippet: .. After incubation for four hours at 37° C. and 10% of CO2, the cells are fixed (5 min, 4% formaldehyde in PBS), permeabilised (10 min, 0.2% Triton X-100 in PBS) and, after blocking of nonspecific binding sites (10% goat serum, 1% BSA in PBS), incubated overnight at 4° C. with a specific anti-pCHK2 antibody (cell signalling #2661). pCHK2 (Thr68) is determined using an Alexa488-labelled secondary anti-rabbit IgG antibody. ..

    Article Title: ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.
    Article Snippet: The protein was extracted by 12000 g centrifugation for 15 min at 4 C. The concentration of protein was detected by Pierce BCA Protein Assay Kit (#23225, Thermo) and recorded by Infinite M Nano System (Tecan) at 570 nm. .. Protein samples were loaded to 8%–12% SDS-PAGE gels, and run the samples with 80–120 V for 1 h. Then transferred into 0.22 μm PVDF membrane with 250 mA for 1.5–4 h. Blocked the membrane with 5% BSA in TBST for 1 h on a shaker and incubated with a specific primary antibodies pATR (S428) (1:1000, #178407, Abcam), ATR (1:1000, #13934S, CST), pChk1 (S345) (1:1000, #2348S, CST), Chk1 (1:1000, #32531, Abcam), pATM (S1981) (1:1000, #5883S, CST), ATM (1:1000, #2873S, CST), pChk2 (Thr68) (1:1000, #2197S, CST), Chk2 (1:1000, #6334S, CST), γ-H2AX (1:1000, #2577S, CST), H2AX (1:1000, #7631S, CST), GAPDH (1:10000, #60004-1-Ig, Proteintech), HSP90 (1:10000, #60318-1-Ig, Proteintech), FLAG (1:1000, #F1804, Sigma-Aldrich), TopBP1 (1:1000, # A300-111A, Bethyl), Claspin (1:400, #23206-1-AP, Proteintech), ATRIP (1:1000, #11327-1-AP, Proteintech), Histone-H3 (1:1000, #17168-1-AP, Proteintech) overnight at 4 C. Washed the membrane with TBST three times, incubated with HRP-conjugated secondary antibody at room temperature for 1 h. Washed the membrane with TBST three times and detected the signal with SuperSignal Western Blot Enhancer (#46640, Thermo) and Chemi XX9 imaging system (SYNGENE). .. The quantifications of protein gray-values were calculated by ImageJ software.

    Article Title: Exploring the role of PARP1 inhibition in enhancing antibody–drug conjugate therapy for acute leukemias: insights from DNA damage response pathway interactions
    Article Snippet: The percentage of phospho-H2AX-positive cells was quantified using Attune Nxt Flow cytometer (ThermoFisher Scientific) The remaining cells were cultured for additional 21 h (total 24 h) and then counted by Trypan blue exclusion assay (Sigma Aldrich) to evaluate the cell viability. .. Immunoblotting analyses were performed using Mini-Protean TGX stain-free precast gels, blotted to nitrocellulose membranes (Bio-Rad, Hercules, CA, USA) and incubated the following antibodies: pATR Ser428 (#2853); pATM Ser1981 (#5883); pCHK2 Thr68 (#2661); pCHK1 Ser345 (#2348); pWEE1 Ser642 (#4910); ATM (#2873); ATR (#13934); CHK1 (#37010); CHK2 (#2662); WEE1 (#13,084); BRCA1 (#9010); BRCA2 (#10741); PALB2 (#30253); KU70 (#4588); XLF (#2854); PCNA (#13110); PARP1 (#9542); CCNB1 (#4138); pCDK1 Tyr15 (#9111); pH2AX Ser139 (#2577); all from Cell Signaling Technologies (Danvers, MA, USA). .. The signal was detected using the enhanced chemiluminescence kit ECL (Bio-Rad, Hercules, CA, USA) and the compact darkroom ChemiDoc-It (Bio-Rad, Hercules, CA, USA).

    Blocking Assay:

    Article Title: Imidazolonylquinoline compounds and therapeutic uses thereof
    Article Snippet: .. After incubation for four hours at 37° C. and 10% of CO2, the cells are fixed (5 min, 4% formaldehyde in PBS), permeabilised (10 min, 0.2% Triton X-100 in PBS) and, after blocking of nonspecific binding sites (10% goat serum, 1% BSA in PBS), incubated overnight at 4° C. with a specific anti-pCHK2 antibody (cell signalling #2661). pCHK2 (Thr68) is determined using an Alexa488-labelled secondary anti-rabbit IgG antibody. ..

    Binding Assay:

    Article Title: Imidazolonylquinoline compounds and therapeutic uses thereof
    Article Snippet: .. After incubation for four hours at 37° C. and 10% of CO2, the cells are fixed (5 min, 4% formaldehyde in PBS), permeabilised (10 min, 0.2% Triton X-100 in PBS) and, after blocking of nonspecific binding sites (10% goat serum, 1% BSA in PBS), incubated overnight at 4° C. with a specific anti-pCHK2 antibody (cell signalling #2661). pCHK2 (Thr68) is determined using an Alexa488-labelled secondary anti-rabbit IgG antibody. ..

    other:

    Article Title: APOBEC3B enhances the efficacy of PARP inhibitors in elimination of ovarian cancer stem cell
    Article Snippet: The following antibodies were used: APOBEC3B (Abcam, Cat #ab184990; RRID:AB_2891094); CD133-APC (Biolegend, Cat #397,906; RRID:AB_2876721); SOX2 (Abcam, Cat #ab92494; RRID:AB_10585428); PARP (Abcam Cat #ab191217; RRID:AB_2861274); Cleaved PARP (Abcam Cat #ab32561; RRID:AB_777103); γH2AX (S139) (Abcam, Cat #ab11174; RRID:AB_297813); Chk1 (Abcam, Cat #ab40866; RRID:AB_726820); pChk1 (S317) (Abcam, Cat #ab278717); UNG (Origene, Cat #TA503563; RRID:AB_11126624); pATR (S428) (Cell Signaling, Cat #2853); pATM (S1981) (Cell Signaling, Cat #13,050); pChk2 (Thr68) (Cell Signaling, Cat #2197); phosphor-p53 (S15) (Cell Signaling, Cat #9286); pBRCA1 (S1524) (Cell Signaling, Cat #9009); beta-actin (Abcam, Cat #ab8227; RRID: AB_2305186); Goat anti-Rabbit Alexa488 secondary antibody (ThermoFisher, Cat #A32731; RRID: AB_2633280); Goat anti-Rabbit Alexa647 secondary antibody (ThermoFisher, Cat #32,733; RRID: AB_2633282).

    SDS Page:

    Article Title: ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.
    Article Snippet: The protein was extracted by 12000 g centrifugation for 15 min at 4 C. The concentration of protein was detected by Pierce BCA Protein Assay Kit (#23225, Thermo) and recorded by Infinite M Nano System (Tecan) at 570 nm. .. Protein samples were loaded to 8%–12% SDS-PAGE gels, and run the samples with 80–120 V for 1 h. Then transferred into 0.22 μm PVDF membrane with 250 mA for 1.5–4 h. Blocked the membrane with 5% BSA in TBST for 1 h on a shaker and incubated with a specific primary antibodies pATR (S428) (1:1000, #178407, Abcam), ATR (1:1000, #13934S, CST), pChk1 (S345) (1:1000, #2348S, CST), Chk1 (1:1000, #32531, Abcam), pATM (S1981) (1:1000, #5883S, CST), ATM (1:1000, #2873S, CST), pChk2 (Thr68) (1:1000, #2197S, CST), Chk2 (1:1000, #6334S, CST), γ-H2AX (1:1000, #2577S, CST), H2AX (1:1000, #7631S, CST), GAPDH (1:10000, #60004-1-Ig, Proteintech), HSP90 (1:10000, #60318-1-Ig, Proteintech), FLAG (1:1000, #F1804, Sigma-Aldrich), TopBP1 (1:1000, # A300-111A, Bethyl), Claspin (1:400, #23206-1-AP, Proteintech), ATRIP (1:1000, #11327-1-AP, Proteintech), Histone-H3 (1:1000, #17168-1-AP, Proteintech) overnight at 4 C. Washed the membrane with TBST three times, incubated with HRP-conjugated secondary antibody at room temperature for 1 h. Washed the membrane with TBST three times and detected the signal with SuperSignal Western Blot Enhancer (#46640, Thermo) and Chemi XX9 imaging system (SYNGENE). .. The quantifications of protein gray-values were calculated by ImageJ software.

    Membrane:

    Article Title: ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.
    Article Snippet: The protein was extracted by 12000 g centrifugation for 15 min at 4 C. The concentration of protein was detected by Pierce BCA Protein Assay Kit (#23225, Thermo) and recorded by Infinite M Nano System (Tecan) at 570 nm. .. Protein samples were loaded to 8%–12% SDS-PAGE gels, and run the samples with 80–120 V for 1 h. Then transferred into 0.22 μm PVDF membrane with 250 mA for 1.5–4 h. Blocked the membrane with 5% BSA in TBST for 1 h on a shaker and incubated with a specific primary antibodies pATR (S428) (1:1000, #178407, Abcam), ATR (1:1000, #13934S, CST), pChk1 (S345) (1:1000, #2348S, CST), Chk1 (1:1000, #32531, Abcam), pATM (S1981) (1:1000, #5883S, CST), ATM (1:1000, #2873S, CST), pChk2 (Thr68) (1:1000, #2197S, CST), Chk2 (1:1000, #6334S, CST), γ-H2AX (1:1000, #2577S, CST), H2AX (1:1000, #7631S, CST), GAPDH (1:10000, #60004-1-Ig, Proteintech), HSP90 (1:10000, #60318-1-Ig, Proteintech), FLAG (1:1000, #F1804, Sigma-Aldrich), TopBP1 (1:1000, # A300-111A, Bethyl), Claspin (1:400, #23206-1-AP, Proteintech), ATRIP (1:1000, #11327-1-AP, Proteintech), Histone-H3 (1:1000, #17168-1-AP, Proteintech) overnight at 4 C. Washed the membrane with TBST three times, incubated with HRP-conjugated secondary antibody at room temperature for 1 h. Washed the membrane with TBST three times and detected the signal with SuperSignal Western Blot Enhancer (#46640, Thermo) and Chemi XX9 imaging system (SYNGENE). .. The quantifications of protein gray-values were calculated by ImageJ software.

    Western Blot:

    Article Title: ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.
    Article Snippet: The protein was extracted by 12000 g centrifugation for 15 min at 4 C. The concentration of protein was detected by Pierce BCA Protein Assay Kit (#23225, Thermo) and recorded by Infinite M Nano System (Tecan) at 570 nm. .. Protein samples were loaded to 8%–12% SDS-PAGE gels, and run the samples with 80–120 V for 1 h. Then transferred into 0.22 μm PVDF membrane with 250 mA for 1.5–4 h. Blocked the membrane with 5% BSA in TBST for 1 h on a shaker and incubated with a specific primary antibodies pATR (S428) (1:1000, #178407, Abcam), ATR (1:1000, #13934S, CST), pChk1 (S345) (1:1000, #2348S, CST), Chk1 (1:1000, #32531, Abcam), pATM (S1981) (1:1000, #5883S, CST), ATM (1:1000, #2873S, CST), pChk2 (Thr68) (1:1000, #2197S, CST), Chk2 (1:1000, #6334S, CST), γ-H2AX (1:1000, #2577S, CST), H2AX (1:1000, #7631S, CST), GAPDH (1:10000, #60004-1-Ig, Proteintech), HSP90 (1:10000, #60318-1-Ig, Proteintech), FLAG (1:1000, #F1804, Sigma-Aldrich), TopBP1 (1:1000, # A300-111A, Bethyl), Claspin (1:400, #23206-1-AP, Proteintech), ATRIP (1:1000, #11327-1-AP, Proteintech), Histone-H3 (1:1000, #17168-1-AP, Proteintech) overnight at 4 C. Washed the membrane with TBST three times, incubated with HRP-conjugated secondary antibody at room temperature for 1 h. Washed the membrane with TBST three times and detected the signal with SuperSignal Western Blot Enhancer (#46640, Thermo) and Chemi XX9 imaging system (SYNGENE). .. The quantifications of protein gray-values were calculated by ImageJ software.

    Article Title: Exploring the role of PARP1 inhibition in enhancing antibody–drug conjugate therapy for acute leukemias: insights from DNA damage response pathway interactions
    Article Snippet: The percentage of phospho-H2AX-positive cells was quantified using Attune Nxt Flow cytometer (ThermoFisher Scientific) The remaining cells were cultured for additional 21 h (total 24 h) and then counted by Trypan blue exclusion assay (Sigma Aldrich) to evaluate the cell viability. .. Immunoblotting analyses were performed using Mini-Protean TGX stain-free precast gels, blotted to nitrocellulose membranes (Bio-Rad, Hercules, CA, USA) and incubated the following antibodies: pATR Ser428 (#2853); pATM Ser1981 (#5883); pCHK2 Thr68 (#2661); pCHK1 Ser345 (#2348); pWEE1 Ser642 (#4910); ATM (#2873); ATR (#13934); CHK1 (#37010); CHK2 (#2662); WEE1 (#13,084); BRCA1 (#9010); BRCA2 (#10741); PALB2 (#30253); KU70 (#4588); XLF (#2854); PCNA (#13110); PARP1 (#9542); CCNB1 (#4138); pCDK1 Tyr15 (#9111); pH2AX Ser139 (#2577); all from Cell Signaling Technologies (Danvers, MA, USA). .. The signal was detected using the enhanced chemiluminescence kit ECL (Bio-Rad, Hercules, CA, USA) and the compact darkroom ChemiDoc-It (Bio-Rad, Hercules, CA, USA).

    Article Title: Repurposing the anthelmintic drug mebendazole in combination with radiation therapy in an isocitrate dehydrogenase mutant glioma model
    Article Snippet: Protein concentration was measured using the BCA protein kit assay (ThermoFisher). .. Western blot was performed as previously described., The following primary antibodies were used: pAurora B(thr232), Aurora, pATM(ser1981), ATM, BAK, BAX, BCL2, pCDK1(tyr15), pChk2(thr68), Cyclin B1, ERK1/2, pERK1/2(thr202/tyr204), Gapdh, pɣH2AX(ser139), MCL-1, MEK1/2, pMEK1/2(ser217/221), P21, P53, α/β-tubulin (Cell Signaling Technology) and Cyclin B2 (Santa Cruz Biotechnology). .. The antigen–antibody complexes were visualized using a horseradish peroxidase-conjugated secondary antibody (Cell Signaling) and Supersignal Thermo West Pico Plus chemiluminescence system (Thermo Scientific).

    Imaging:

    Article Title: ATR/Chk1 interacting lncRNA modulates DNA damage response to induce breast cancer chemoresistance.
    Article Snippet: The protein was extracted by 12000 g centrifugation for 15 min at 4 C. The concentration of protein was detected by Pierce BCA Protein Assay Kit (#23225, Thermo) and recorded by Infinite M Nano System (Tecan) at 570 nm. .. Protein samples were loaded to 8%–12% SDS-PAGE gels, and run the samples with 80–120 V for 1 h. Then transferred into 0.22 μm PVDF membrane with 250 mA for 1.5–4 h. Blocked the membrane with 5% BSA in TBST for 1 h on a shaker and incubated with a specific primary antibodies pATR (S428) (1:1000, #178407, Abcam), ATR (1:1000, #13934S, CST), pChk1 (S345) (1:1000, #2348S, CST), Chk1 (1:1000, #32531, Abcam), pATM (S1981) (1:1000, #5883S, CST), ATM (1:1000, #2873S, CST), pChk2 (Thr68) (1:1000, #2197S, CST), Chk2 (1:1000, #6334S, CST), γ-H2AX (1:1000, #2577S, CST), H2AX (1:1000, #7631S, CST), GAPDH (1:10000, #60004-1-Ig, Proteintech), HSP90 (1:10000, #60318-1-Ig, Proteintech), FLAG (1:1000, #F1804, Sigma-Aldrich), TopBP1 (1:1000, # A300-111A, Bethyl), Claspin (1:400, #23206-1-AP, Proteintech), ATRIP (1:1000, #11327-1-AP, Proteintech), Histone-H3 (1:1000, #17168-1-AP, Proteintech) overnight at 4 C. Washed the membrane with TBST three times, incubated with HRP-conjugated secondary antibody at room temperature for 1 h. Washed the membrane with TBST three times and detected the signal with SuperSignal Western Blot Enhancer (#46640, Thermo) and Chemi XX9 imaging system (SYNGENE). .. The quantifications of protein gray-values were calculated by ImageJ software.

    Staining:

    Article Title: Exploring the role of PARP1 inhibition in enhancing antibody–drug conjugate therapy for acute leukemias: insights from DNA damage response pathway interactions
    Article Snippet: The percentage of phospho-H2AX-positive cells was quantified using Attune Nxt Flow cytometer (ThermoFisher Scientific) The remaining cells were cultured for additional 21 h (total 24 h) and then counted by Trypan blue exclusion assay (Sigma Aldrich) to evaluate the cell viability. .. Immunoblotting analyses were performed using Mini-Protean TGX stain-free precast gels, blotted to nitrocellulose membranes (Bio-Rad, Hercules, CA, USA) and incubated the following antibodies: pATR Ser428 (#2853); pATM Ser1981 (#5883); pCHK2 Thr68 (#2661); pCHK1 Ser345 (#2348); pWEE1 Ser642 (#4910); ATM (#2873); ATR (#13934); CHK1 (#37010); CHK2 (#2662); WEE1 (#13,084); BRCA1 (#9010); BRCA2 (#10741); PALB2 (#30253); KU70 (#4588); XLF (#2854); PCNA (#13110); PARP1 (#9542); CCNB1 (#4138); pCDK1 Tyr15 (#9111); pH2AX Ser139 (#2577); all from Cell Signaling Technologies (Danvers, MA, USA). .. The signal was detected using the enhanced chemiluminescence kit ECL (Bio-Rad, Hercules, CA, USA) and the compact darkroom ChemiDoc-It (Bio-Rad, Hercules, CA, USA).



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