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anti p38  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc anti p38
    Anti P38, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 97/100, based on 3188 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+p38+antibody/p38+MAPK+XP+Rabbit+mAb/pm42810528-62-55-57
    Average 97 stars, based on 3188 article reviews
    anti p38 - by Bioz Stars, 2026-10
    97/100 stars

    Images

    Related Articles

    other:

    Article Title: Arrestin-3-assisted activation of JNK3 mediates dopaminergic behavioral sensitization
    Article Snippet: Rabbit anti p38 antibody , Cell Signaling Technologies , Cat#9212 RRID: AB_330713.

    Nucleic Acid Electrophoresis:

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation.
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit antiphospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit anti-phospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).

    Membrane:

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation.
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit antiphospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit anti-phospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).

    Saline:

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation.
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit antiphospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).

    Article Title: Casein kinase-2 inhibition promotes retinal ganglion cell survival after acute intraocular pressure elevation
    Article Snippet: Three retinas per group were homogenized in radioimmunoprecipitation assay lysis buffer (Solarbio) containing protease and phosphatase inhibitors. .. Next, 50 μg of total protein was resolved by SDS-polyacrylamide gel electrophoresis (Bio-Rad, Hercules, CA, USA), transferred onto a nitrocellulose membrane (Amersham Biosciences, Little Chalfont, UK), blocked with 5% skim milk in 0.05% Tween 20 (ICN, Erie, PA, USA) in Tris-buffered saline, and probed with rabbit anti-extracellular-signal-regulated kinase (Erk) p44/p42 antibody (1:1000, Cell Signaling Technology, Beverly, MA, USA, Cat# 4695, RRID: AB_390779), rabbit anti-phospho-Erk p44/p42 antibody (1:1000, Cell Signaling Technology, Cat# 8544, RRID: AB_11127856), rabbit anti-p38 antibody (1:1000, Cell Signaling Technology, Cat# 14451, RRID: AB_2798482), or rabbit anti-phospho-p38 antibody (1:1000, Cell Signaling Technology, Cat# 4511, RRID: AB_2139682) in 3% bovine serum albumin at 4°C overnight. .. After washing in tris buffered saline, the membranes were incubated with corresponding donkey horseradish peroxidase-conjugated secondary antibody (1:1000, Amersham Biosciences, Little Chalfont, UK, Cat# NA934, RRID: AB_772206) for 1 hour at room temperature (25°C), and the signals were detected by electrochemiluminescence (Pierce, Rockford, IL, USA).



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    Image Search Results


    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Article Snippet: Membranes were blocked with 5 % BSA at 37°C for 2 h and incubated overnight at 4°C with the following primary antibodies: ITGAV Rabbit Ab, PLC Rabbit Ab, p-PLC Rabbit Ab, p-p65 Rabbit Ab, and Bcl2 Rabbit Ab were purchased from Bioss (Beijing, China); FAK Rabbit Ab, p-FAK Rabbit Ab, ERK Rabbit Ab, p-ERK Rabbit Ab, JNK Rabbit Ab, p-JNK Rabbit Ab, p38 MAPK Rabbit Ab, p-p38 MAPK Rabbit Ab, PI3K Rabbit Ab, p-PI3K Rabbit Ab, AKT Rabbit Ab, p-AKT Rabbit Ab, PKC Rabbit Ab, p-PKC Rabbit Ab, Bax Rabbit Ab, and Caspase 3 Rabbit Ab were purchased from Abmart (Shanghai, China); p65 Rabbit Ab (Proteintech, Wuhan, China).

    Techniques: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Article Snippet: Membranes were blocked with 5 % BSA at 37°C for 2 h and incubated overnight at 4°C with the following primary antibodies: ITGAV Rabbit Ab, PLC Rabbit Ab, p-PLC Rabbit Ab, p-p65 Rabbit Ab, and Bcl2 Rabbit Ab were purchased from Bioss (Beijing, China); FAK Rabbit Ab, p-FAK Rabbit Ab, ERK Rabbit Ab, p-ERK Rabbit Ab, JNK Rabbit Ab, p-JNK Rabbit Ab, p38 MAPK Rabbit Ab, p-p38 MAPK Rabbit Ab, PI3K Rabbit Ab, p-PI3K Rabbit Ab, AKT Rabbit Ab, p-AKT Rabbit Ab, PKC Rabbit Ab, p-PKC Rabbit Ab, Bax Rabbit Ab, and Caspase 3 Rabbit Ab were purchased from Abmart (Shanghai, China); p65 Rabbit Ab (Proteintech, Wuhan, China).

    Techniques: Activity Assay

    The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The mRNA expression of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2 , and Caspase 3 in E.tenella host cells.

    Article Snippet: p-p38 MAPK Rabbit Ab , Abmart , TA4001 , 1: 1500.

    Techniques: Expressing

    The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Journal: Poultry Science

    Article Title: Pathogenic mechanism of Eimeria tenella Et MIC2 promotes Eimeria tenella invasion and inhibits host cell apoptosis through binding to the ITGAV receptor

    doi: 10.1016/j.psj.2026.106922

    Figure Lengend Snippet: The protein activity changes of ITGAV, FAK, PLC, PKC, p65, ERK, JNK, p38, PI3K, Akt, Bax, Bcl2, and Caspase 3 in E.tenella host cells.

    Article Snippet: p-p38 MAPK Rabbit Ab , Abmart , TA4001 , 1: 1500.

    Techniques: Activity Assay

    Cytokines Activated Their Downstream Pathways in HK-2 Cells. The phosphorylation of ERK, JNK, p38, and NF-κB in HK-2 cells treated with TNF-α (A) or IL-1β (B) was analyzed over a time course ranging from 15 min to 4 h. The phosphorylation of Smad1/5/9 and Smad2/3 in HK-2 cells treated with TGF-β1 (C) or BMP-2 (D) was analyzed over a time course ranging from 15 min to 4 h. GAPDH was served as the loading control.

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Inflammation-induced osteogenic signaling promotes calcium phosphate crystal formation in kidneys via MAPK, NF-κB, and smad pathways

    doi: 10.3389/fcell.2026.1831072

    Figure Lengend Snippet: Cytokines Activated Their Downstream Pathways in HK-2 Cells. The phosphorylation of ERK, JNK, p38, and NF-κB in HK-2 cells treated with TNF-α (A) or IL-1β (B) was analyzed over a time course ranging from 15 min to 4 h. The phosphorylation of Smad1/5/9 and Smad2/3 in HK-2 cells treated with TGF-β1 (C) or BMP-2 (D) was analyzed over a time course ranging from 15 min to 4 h. GAPDH was served as the loading control.

    Article Snippet: Primary antibodies for immunoblotting such as OPN (A19092), ALP (A0514), OPG (A2100), Runx2 (A2851), p-JNK1/2/3 (AP0631), JNK1/2/3 (A4867), p-NF-κB (AP0944), NF-κB (A19653), p-p38 (AP0057), p38 (A14401), p-ERK (AP0485), ERK (A4782), p-Smad1/5/9 (AP0850), Smad1 (A21734), p-Smad2/3 (AP0548), Smad2/3 (A7536), TNF-α (A11534), IL-1β (A11534), TGF-β1 (A16640), BMP-2 (A0231), β-actin (AC028), α-Tubulin (A6830), and GAPDH (A19056) were from ABclonal (Woburn, MA, United States).

    Techniques: Phospho-proteomics, Control

    Pro-inflammatory Cytokines Upregulated Osteogenesis-related Proteins via the MAPK/NF-κB and Smad Signaling Pathway. HK-2 cells were pretreated with 10 µM ERK inhibitor (U0126), JNK inhibitor (SP600125), p38 inhibitor (SB203580), or NF-κB inhibitor (BAY 11–7,082) for 2 h, and then treated with 20 ng/mL TNF-α (A) or IL-1β (B) for 72 h (C) HK-2 cells were pretreated with 5 µM Smad2/3 inhibitor (SB-525334) for 2 h and then treated with 200 ng/mL TGF-β1 for 72 h (D) HK-2 cells were pretreated with 10 µM Smad1/5/8 inhibitor (LDN-193189) for 2 h and then treated with 100 ng/mL BMP-2 for 72 h. The expression of osteoblast markers (ALP, OPN, and OPG) was examined by Western blotting. The quantitative results showed the fold change of the protein expression compared to the control group. GAPDH served as the loading control. Data are presented as individual data points (scatter plot) with the mean ± SEM; n = 3; * P < 0.05, ** P < 0.01, *** P < 0.001 versus the control group; # P < 0.05, ## P < 0.01, ### P < 0.001 versus cytokine group (One-way ANOVA).

    Journal: Frontiers in Cell and Developmental Biology

    Article Title: Inflammation-induced osteogenic signaling promotes calcium phosphate crystal formation in kidneys via MAPK, NF-κB, and smad pathways

    doi: 10.3389/fcell.2026.1831072

    Figure Lengend Snippet: Pro-inflammatory Cytokines Upregulated Osteogenesis-related Proteins via the MAPK/NF-κB and Smad Signaling Pathway. HK-2 cells were pretreated with 10 µM ERK inhibitor (U0126), JNK inhibitor (SP600125), p38 inhibitor (SB203580), or NF-κB inhibitor (BAY 11–7,082) for 2 h, and then treated with 20 ng/mL TNF-α (A) or IL-1β (B) for 72 h (C) HK-2 cells were pretreated with 5 µM Smad2/3 inhibitor (SB-525334) for 2 h and then treated with 200 ng/mL TGF-β1 for 72 h (D) HK-2 cells were pretreated with 10 µM Smad1/5/8 inhibitor (LDN-193189) for 2 h and then treated with 100 ng/mL BMP-2 for 72 h. The expression of osteoblast markers (ALP, OPN, and OPG) was examined by Western blotting. The quantitative results showed the fold change of the protein expression compared to the control group. GAPDH served as the loading control. Data are presented as individual data points (scatter plot) with the mean ± SEM; n = 3; * P < 0.05, ** P < 0.01, *** P < 0.001 versus the control group; # P < 0.05, ## P < 0.01, ### P < 0.001 versus cytokine group (One-way ANOVA).

    Article Snippet: Primary antibodies for immunoblotting such as OPN (A19092), ALP (A0514), OPG (A2100), Runx2 (A2851), p-JNK1/2/3 (AP0631), JNK1/2/3 (A4867), p-NF-κB (AP0944), NF-κB (A19653), p-p38 (AP0057), p38 (A14401), p-ERK (AP0485), ERK (A4782), p-Smad1/5/9 (AP0850), Smad1 (A21734), p-Smad2/3 (AP0548), Smad2/3 (A7536), TNF-α (A11534), IL-1β (A11534), TGF-β1 (A16640), BMP-2 (A0231), β-actin (AC028), α-Tubulin (A6830), and GAPDH (A19056) were from ABclonal (Woburn, MA, United States).

    Techniques: Expressing, Western Blot, Control