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perk1 2  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc perk1 2

    Perk1 2, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 16846 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/anti+mapk/Phospho-p44%2F42+MAPK+(Erk1%2F2)+(Thr202%2FTyr204)+Antibody/pmc13669479-12-0-8
    Average 99 stars, based on 16846 article reviews
    perk1 2 - by Bioz Stars, 2026-10
    99/100 stars

    Images

    1) Product Images from "Fc‐Dependent Targeting of the GAS6–MERTK Axis With Monoclonal and Bispecific Antibodies Overcomes Drug Resistance Across EGFR Mutations in Exons 19, 20, and 21"

    Article Title: Fc‐Dependent Targeting of the GAS6–MERTK Axis With Monoclonal and Bispecific Antibodies Overcomes Drug Resistance Across EGFR Mutations in Exons 19, 20, and 21

    Journal: Advanced Science

    doi: 10.1002/advs.78290


    Figure Legend Snippet:

    Techniques Used: Cell-Signaling

    Related Articles

    other:

    Article Title: ecDNA-driven oncogene super-expressors shape immunoevasive tumor microenvironment
    Article Snippet: Protein concentration was determined using the BCA Protein Assay Kit (Thermo Fisher Scientific, A53225).

    Incubation:

    Article Title: Brain-derived neurotrophic factor scales presynaptic calcium transients to modulate excitatory neurotransmission.
    Article Snippet: .. Blots were incubated in anti- TrkB 1:100 (BD Transduction, 610101), anti- pTrkB 1:1,000 (EMD Millipore, ABN1381), anti- MAPK 1:20,000 (Cell Signaling, 9102), anti- pMAPK 1:20,000 (Cell Signaling, 9101), anti- GAPDH 1:50,000 (Cell Signaling, 2118), synaptobrevin- 2 1:5,000 (Synaptic Systems, 104 211), and Rab- GDI1 1:2,000 (Synaptic Systems, 130 011) with 1% BSA in TBST overnight at 4 °C. .. After three washes in TBS, anti- mouse secondary antibody for TrkB (1:10,000), anti- rabbit secondary antibody for pTrkB (1:15,000), and anti- rabbit secondary for all others at 1:25,000 dilution were incubated for 2 h at room temperature (IRDye Secondary Antibodies, Li- Cor).

    Article Title: Endosialin promotes vascular maturation by inhibiting Cyr61 expression in melanoma metastasis
    Article Snippet: Every protein sample was loaded on 8% SDS- PAGE and then transferred into a PVDF membrane (ThermoFisher Scientific). .. And then membrane incubated with primary antibodies overnight at 4°C: anti-EN (#ab48185, Abcam), anti-Cyr61 (#ab230947, Abcam), anti-GAPDH (#10494-1-AP, Proteintech), anti-p-MAPK (#4370T, CST), and anti-MAPK (#4695T, CST). ..

    Article Title: Vasorin (VASN) overexpression promotes pulmonary metastasis and resistance to adjuvant chemotherapy in patients with locally advanced rectal cancer
    Article Snippet: The proteins were added to 5x loading buffer (FDbio, Cat# FD006) and boiled at 100 °C for 10 min. Proteins were separated through SDS‒PAGE (EpiZyme) and then transferred to 0.22–0.45 μm PVDF membranes (Merck Millipore). .. The membranes were blocked with 5% nonfat milk for 1 h and incubated with the following primary antibodies: anti-β-actin (Proteintech, Cat# 20536-1-AP, 1:1000), anti-VASN (Abcam, Cat# ab156868, 1:1000), anti-N-cadherin (MCE, Cat# HY-P80238, 1:1000), anti-E-cadherin (MCE, Cat# HY-P80112, 1:1000), anti-β-catenin (MCE, Cat# HY-P80488, 1:1000), anti-CDK1 (Affinity Biosciences, Cat# CDK1/CDC2, 1:1000), anti- Cyclin B1 (Affinity Biosciences, Cat# Cyclin B1, 1:1000), anti-NOTCH1 (CST, Cat# 3608 S, 1:1000), anti-NICD (NOTCH1 intracellular domain, cleaved form of NOTCH1) (CST, Cat# 4147T, 1:1000), anti-MAPK (CST, Cat# 9926T, 1:1000), and anti-phospho-MAPK (CST, Cat# 9910T, 1:1000) antibodies overnight. .. Next, the membranes were incubated with HRP-conjugated secondary antibodies (Proteintech, Cat# SA00001-1/SA00001-2, 1:5000) for 1 h, and then the protein expression levels were visualized via chemiluminescence.

    Article Title: Vasorin (VASN) overexpression promotes pulmonary metastasis and resistance to adjuvant chemotherapy in patients with locally advanced rectal cancer.
    Article Snippet: The proteins were added to 5x loading buffer (FDbio, Cat# FD006) and boiled at 100 °C for 10 min. Proteins were separated through SDS‒PAGE (EpiZyme) and then transferred to 0.22–0.45 μm PVDF membranes (Merck Millipore). .. The membranes were blocked with 5% nonfat milk for 1 h and incubated with the following primary antibodies: anti-β-actin (Proteintech, Cat# 20536-1-AP, 1:1000), anti-VASN (Abcam, Cat# ab156868, 1:1000), anti-N-cadherin (MCE, Cat# HY-P80238, 1:1000), anti-E-cadherin (MCE, Cat# HY-P80112, 1:1000), anti-β-catenin (MCE, Cat# HY-P80488, 1:1000), anti-CDK1 (Affinity Biosciences, Cat# CDK1/CDC2, 1:1000), anti- Cyclin B1 (Affinity Biosciences, Cat# Cyclin B1, 1:1000), anti-NOTCH1 (CST, Cat# 3608 S, 1:1000), anti-NICD (NOTCH1 intracellular domain, cleaved form of NOTCH1) (CST, Cat# 4147T, 1:1000), anti-MAPK (CST, Cat# 9926T, 1:1000), and anti-phospho-MAPK (CST, Cat# 9910T, 1:1000) antibodies overnight. .. Next, the membranes were incubated with HRP-conjugated secondary antibodies (Proteintech, Cat# SA00001-1/SA00001-2, 1:5000) for 1 h, and then the protein expression levels were visualized via chemiluminescence.

    Membrane:

    Article Title: Endosialin promotes vascular maturation by inhibiting Cyr61 expression in melanoma metastasis
    Article Snippet: Every protein sample was loaded on 8% SDS- PAGE and then transferred into a PVDF membrane (ThermoFisher Scientific). .. And then membrane incubated with primary antibodies overnight at 4°C: anti-EN (#ab48185, Abcam), anti-Cyr61 (#ab230947, Abcam), anti-GAPDH (#10494-1-AP, Proteintech), anti-p-MAPK (#4370T, CST), and anti-MAPK (#4695T, CST). ..

    Western Blot:

    Article Title: Stat3 -mediated Th17 pathogenicity induced by periodontitis contributes to cognitive impairment by promoting microglial M1 polarization
    Article Snippet: .. Western Blot antibodies: anti-MAPK (4312, Cell Signaling Technology, USA); Anti-pMAPK (9211S, Cell Signaling Technology, USA); Anti-ERK (4695, Cell Signaling Technology, USA); Anti-pERK (4370, Cell Signaling Technology, USA); Anti-GAPDH (AF0006, Beyotime, China); HRP-labeled Goat Anti-Rabbit (AF0208, Beyotime, China); HRP-labeled Goat Anti-Mouse (AF0216, Beyotime, China). ..

    Cell-Signaling:

    Article Title: Stat3 -mediated Th17 pathogenicity induced by periodontitis contributes to cognitive impairment by promoting microglial M1 polarization
    Article Snippet: .. Western Blot antibodies: anti-MAPK (4312, Cell Signaling Technology, USA); Anti-pMAPK (9211S, Cell Signaling Technology, USA); Anti-ERK (4695, Cell Signaling Technology, USA); Anti-pERK (4370, Cell Signaling Technology, USA); Anti-GAPDH (AF0006, Beyotime, China); HRP-labeled Goat Anti-Rabbit (AF0208, Beyotime, China); HRP-labeled Goat Anti-Mouse (AF0216, Beyotime, China). ..



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    Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, <t>p‐ERK1/2</t> (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .
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    Effects of L-lactate and GPR81 agonist on ATP levels in primary hippocampal cells. (a) Exemplary immunoblotting analysis and bar graphs depict the quantified protein levels (normalized to CON) for GPR81, derived from three independent replicates. (b) Representative immunoblots of <t>p-ERK1/2</t> and t-ERK1/2, and quantification normalized to CON, derived from three independent replicates. (c) Quantification of relative ATP levels, derived from three independent replicates. Data are expressed as mean ± SD. Statistical significance: ** p < 0.01, *** p < 0.001 versus the CON group.
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    Image Search Results


    Journal: Advanced Science

    Article Title: Fc‐Dependent Targeting of the GAS6–MERTK Axis With Monoclonal and Bispecific Antibodies Overcomes Drug Resistance Across EGFR Mutations in Exons 19, 20, and 21

    doi: 10.1002/advs.78290

    Figure Lengend Snippet:

    Article Snippet: pERK1/2 (Thr202/Tyr204) , 9101S , Cell Signaling Technology (CST) , AB_331646.

    Techniques: Cell-Signaling

    Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Journal: Pigment Cell & Melanoma Research

    Article Title: Allele‐Specific GNAQ Q209 Mutations Reveal Context‐Dependent Oncogenic Programs in Uveal Melanoma

    doi: 10.1111/pcmr.70121

    Figure Lengend Snippet: Q209R preferentially engages FAK‐YAP signaling. (A) Western blot analysis of GNAQ, BAP1, Melan‐A, p‐ERK1/2 (Thr202/Tyr204), ERK1/2, FRA1, p‐AKT (Ser473), AKT, p‐4EBP1 (Ser65), and 4EBP1 expression in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (B) Quantification of the relative ratio between p‐AKT (Ser473) and AKT in Q209R and Q209L UM cell lines from (A). (C) Quantification of the relative ratio between p‐4EBP1 (Ser65) and 4EBP1 in Q209R and Q209L UM cell lines from (A). (D) Western blot analysis of p‐FAK (Tyr397), FAK, p‐YAP (Ser127), and YAP in mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . HSP90 was used as an internal loading control. (E) Quantification of the relative ratio between p‐FAK (Tyr397) and FAK in Q209R and Q209L UM cell lines from (D). (F) Quantification of the relative ratio between p‐YAP (Ser127) and YAP in Q209R and Q209L UM cell lines from (D). Orthotopic tumor‐derived cell lines (QBM12.1 [Q209R], QBM12.3 [Q209R], QBM24 [Q209R], QBM45 [Q209L], QBM47 [Q209L]) and liver metastatic lines (QBM12L [Q209R], QBM12L2 [Q209R], QBM51L [Q209L], QBM53L [Q209L]) were used in A–F. (G) Representative IHC images showing YAP expression in primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (H) Quantification of the nuclear‐to‐cytoplasmic YAP intensity ratio (H‐score) among primary tumors from Gnaq CA ; Bap1 CKO ; Myc CKI mice harboring either GNAQ Q209R or GNAQ Q209L . (I) Representative IHC images showing YAP expression in liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L . (J) Quantification of nuclear YAP intensity (H‐score) among liver metastasis derived from intrasplenic transplantation of mouse UM cell lines harboring GNAQ Q209R or GNAQ Q209L .

    Article Snippet: Antibodies against GNAQ (CST, #14373, RRID:AB_2665457), BAP1 (Abcam, ab255611), Melan‐A (Abcam, ab210546, RRID:AB_2889292), ERK1/2 (CST, #4695, RRID:AB_390779), p‐ERK1/2 (Thr202/Tyr204) (CST, #4370, RRID:AB_2315112), FRA1 (Abcam, ab252421, RRID:AB_2904513), AKT (CST, #4691, RRID:AB_915783), p‐AKT (Ser473) (CST, #4060, RRID:AB_2315049), p‐FAK (Tyr397) (CST, #8556, RRID:AB_10891442), FAK (CST, #3285, RRID:AB_2269034), 4E‐BP1 (CST, #9452, RRID:AB_331692), p‐4E‐BP1 (Ser65; CST, #9451, RRID:AB_330947), YAP (CST, #4912, RRID:AB_2218911), and p‐YAP (Ser127) (CST, #4911, RRID:AB_2218913) were used at 1:1000 as indicated.

    Techniques: Western Blot, Analysis, Expressing, Control, Derivative Assay, Transplantation Assay

    Effects of L-lactate and GPR81 agonist on ATP levels in primary hippocampal cells. (a) Exemplary immunoblotting analysis and bar graphs depict the quantified protein levels (normalized to CON) for GPR81, derived from three independent replicates. (b) Representative immunoblots of p-ERK1/2 and t-ERK1/2, and quantification normalized to CON, derived from three independent replicates. (c) Quantification of relative ATP levels, derived from three independent replicates. Data are expressed as mean ± SD. Statistical significance: ** p < 0.01, *** p < 0.001 versus the CON group.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Lactate promotes mitochondrial biogenesis and fusion via GPR81 to enhance synaptic plasticity-related protein expression in hippocampal cells

    doi: 10.3389/fcell.2026.1929409

    Figure Lengend Snippet: Effects of L-lactate and GPR81 agonist on ATP levels in primary hippocampal cells. (a) Exemplary immunoblotting analysis and bar graphs depict the quantified protein levels (normalized to CON) for GPR81, derived from three independent replicates. (b) Representative immunoblots of p-ERK1/2 and t-ERK1/2, and quantification normalized to CON, derived from three independent replicates. (c) Quantification of relative ATP levels, derived from three independent replicates. Data are expressed as mean ± SD. Statistical significance: ** p < 0.01, *** p < 0.001 versus the CON group.

    Article Snippet: Following transfer, membranes were blocked and incubated overnight at 4 °C with the indicated primary antibodies: GPR81 (1:400, Sigma, SAB1300790), p-ERK1/2 (1:1000, CST, 4370), ERK1/2 (1:1000, CST, 4695), BDNF (1:1000, Proteintech, 28205-1-AP), SYN (1:1000, CST, 4329), PSD95 (1:1000, CST, 3450), PGC-1α (1:1000, Novus, NBP1-04676SS), NRF1 (1:1000, CST, 46743), NRF2 (1:1000, CST, 12721), TFAM (1:2000, Abcam, ab131607), OPA1 (1:1000, CST, 8047), MFN1 (1:2000, Proteintech, 13798-1-AP), MFN2 (1:1000, CST, 9482), and β-Tubulin (1:2000, Proteintech, 10068-1-AP).

    Techniques: Western Blot, Analysis, Derivative Assay