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p38 mitogen activated protein kinases  (Cell Signaling Technology Inc)


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    Cell Signaling Technology Inc p38 mitogen activated protein kinases
    P38 Mitogen Activated Protein Kinases, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 99/100, based on 30305 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/p38+mitogen+activated+protein+kinase/p38+MAPK+Antibody/pm41811890-78-16-46
    Average 99 stars, based on 30305 article reviews
    p38 mitogen activated protein kinases - by Bioz Stars, 2026-09
    99/100 stars

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    other:

    Article Title: Licorice Flavonoid Extract Ameliorates Intestine Damage in Ulcerative Colitis via MAPK/NF-κB Signaling Modulation and Gut Microbiome Remodeling.
    Article Snippet: The following reagents were procured from Cell Signaling Technology: p38 mitogen-activated protein kinase (p38 MAPK), nuclear factor kappa B (NF-κB), phosphorylated NF-κB (pNF-κB), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), peroxisome proliferatoractivated receptor gamma (PPARγ), and anti-rabbit IgG.

    Article Title: Licorice Flavonoid Extract Ameliorates Intestine Damage in Ulcerative Colitis via MAPK/NF-κB Signaling Modulation and Gut Microbiome Remodeling
    Article Snippet: The following reagents were procured from Cell Signaling Technology: p38 mitogen-activated protein kinase (p38 MAPK), nuclear factor kappa B (NF-κB), phosphorylated NF-κB (p-NF-κB), glyceraldehyde-3-phosphate dehydrogenase (GAPDH), peroxisome proliferator-activated receptor gamma (PPARγ), and anti-rabbit IgG.

    Article Title: Molecular responses in abdominal subcutaneous adipose tissue after a session of endurance exercise: effects of exercise intensity
    Article Snippet: Primary antibodies used were hormone‐sensitive lipase (HSL, #18381, Cell Signalling Technology), phospho‐HSL (Ser565) (pHSL S565 , #4137, Cell Signalling Technology), phospho‐HSL (Ser660) (pHSL S660 , #4126, Cell Signalling Technology), protein kinase B (AKT, #9272, Cell Signalling Technology), phospho‐AKT (Ser473) (pAKT S473 , #9271, Cell Signalling Technology), phospho‐AKT (Thr308) (pAKT T308 , #13038, Cell Signalling Technology), p38 mitogen‐activated protein kinase (P38, #9212, Cell Signalling Technology), phospho‐P38 MAPK (Thr180/Tyr182) (pP38 T180/Y192 , #9211, Cell Signalling Technology), p44/42 MAPK extracellular signal‐regulated kinase (ERK, #4695, Cell Signalling Technology), phospho‐p44/42 MAPK (Thr202/Tyr204) (pERK T202/Y204 , #4376, Cell Signalling Technology), signal transducer and activator of transcription 3 (STAT3, #12640, Cell Signalling Technology) and phospho‐STAT3 (Tyr705) (pSTAT3 Y705 , #9145, Cell Signalling Technology).

    Article Title: Colchicine as a therapeutic possibility for the treatment of pulmonary arterial hypertension (PAH) in a rat model.
    Article Snippet: The right ventricular failure is the most important cause of death in pulmonary arterial hypertension (PAH).. Colchicine, a naturally occurring tricyclic alkaloid, protects against inflammatory diseases by favorable modulation of pro-inflammatory cytokine production.. In our present work, we aimed to clarify the effects of colchicine treatment in PAH, specifically on right ventricular cardiac myocytes.

    Article Title: HJP 272, an endothelin receptor antagonist, and its role in cancer cell migration and invasion
    Article Snippet: The antibodies used were glyceraldehyde-3-phosphate dehydrogenase (GAPDH, Cell Signaling, Beverly, MA, USA # 2118S), endothelin-converting enzyme-1 (ECE-1, Santa Cruz, CA # sc-376018), p38 mitogen-activated protein kinase (p38 MAPK, Cell Signaling #9212S), CDK6 (Santa Cruz # sc-53638), α/β-Tubulin (Cell Signaling #2148S), IL-6 (Cell Signaling # 12153S), Anti-mouse IgG, HRP-linked antibody (Cell Signaling #7076S), Anti-rabbit IgG, HRP-linked antibody (Cell Signaling #7074S).

    Article Title: Molecular responses in abdominal subcutaneous adipose tissue after a session of endurance exercise: effects of exercise intensity
    Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense Cell Signalling Technology), phospho-HSL (Ser660) (pHSLS660, #4126, Cell Signalling Technology), protein kinase B (AKT, #9272, Cell Signalling Technology), phospho-AKT (Ser473) (pAKTS473, #9271, Cell Signalling Technology), phospho-AKT (Thr308) (pAKTT308, #13038, Cell Signalling Technology), p38 mitogen-activated protein kinase (P38, #9212, Cell Signalling Technology), phospho-P38 MAPK (Thr180/Tyr182) (pP38T180/Y192, #9211, Cell Signalling Technology), p44/42MAPK extracellular signal-regulated kinase (ERK, #4695, Cell Signalling Technology), phospho-p44/42MAPK (Thr202/Tyr204) (pERKT202/Y204, #4376, Cell Signalling Technology), signal transducer and activator of transcription 3 (STAT3, #12640, Cell Signalling Technology) and phospho-STAT3 (Tyr705) (pSTAT3Y705, #9145, Cell Signalling Technology).

    Article Title: Inhibition of eEF2 kinase ameliorates hepatic injury induced by ACR through regulation of the MAPK pathway.
    Article Snippet: The primary antibodies used in this study include eukaryotic elongation factor 2 (eEF2) (CAT. ABP58457, Abbkine), Phospho-eEF2 (Thr56) antibody (CAT. ABP58456, Abbkine), eukaryotic elongation factor 2 kinase (eEF2K) (CAT. GTX111496, GeneTex), Sphingosine kinase 1 (SphK1) (CAT. GTX107509, GeneTex), p38 mitogen-activated protein kinase (CAT. 0.8690 S, Cell Signaling Technology), Phosphop38 (CAT. 0.4511 S, Cell Signaling Technology), extracellular signalregulated kinase (ERK1/2) (CAT. 0.4695 S, Cell Signaling Technology), Phospho-ERK1/2 (CAT. 0.4370 S, Cell Signaling Technology), cJun N-terminal kinase (JNK) (CAT. 0.9252 S, Cell Signaling Technology), Phospho-JNK (CAT. 0.4668 T, Cell Signaling Technology), and β-actin (CAT. TA811000, ORIGENE).

    Multiple Displacement Amplification:

    Article Title: Camellia japonica hyperoside exhibits anti-age-related macular degeneration effects in an ARPE-19 cell model by inhibiting apoptosis via JNK-Nrf2/HO-1 activation.
    Article Snippet: .. The primary antibodies used were against the following proteins: B-cell lymphoma-extra large (Bcl-xL; Invitrogen; MA5-15142), Bcl-2 associated agonist of cell death (Bad; Santa Cruz Biotechnology, Dallas, TX, USA; sc-8044), Bcl-2 interacting mediator of cell death (Bim; Santa Cruz Biotechnology; sc-11425), c-Jun N-terminal kinases (JNK; Cell Signaling Technology; 9252S), phosphorylated c-Jun N-terminal kinases (p-JNK; Cell Signaling Technology, Danvers, MA, USA; 9251S), p38 mitogen-activated protein kinase (p38MAPK; Cell Signaling Technology; 9212S), phosphorylated p38 mitogen-activated protein kinases (pp38MAPK; Cell Signaling Technology; 4511S), nuclear factor erythroid 2-related factor 2 (Nrf2; Invitrogen; PA5-2788S), heme oxygenase 1 (HO-1; Invitrogen; PA5-77833), superoxide dismutase type 1 (SOD1; Invitrogen; PA5-85095), 4-hydroxynonenal (4-HNE; Abcam; ab46545), malondialdehyde (MDA; Abcam; ab27642), and glyceraldehyde-3phosphate dehydrogenase (GADPH; Invitrogen; MA5-15738). .. The membrane was washed three times with Tris-buffered saline, and then incubated with an appropriate secondary antibody—Goat anti-rabbit IgG (Jackson ImmunoResearch, West Grove, PA, USA; 111-035-003) or Goat anti-mouse IgG (Jackson ImmunoResearch; 115-035-003)—for 2 h at 4 ◦C.



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    APS influences MAPK signaling pathways in ATO-induced BMSCs. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expressions of p-Jnk and Jnk, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was conducted to detect protein expressions of p-p38 and p38, Gap was served as a loading control, n = 3. (C) Western blotting analysis was applied to detect protein expressions of p-Erk and Erk, β -actin was used as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01 vs control group, # P < 0.05 vs ATO group.

    Journal: Chinese Herbal Medicines

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    doi: 10.1016/j.chmed.2025.03.007

    Figure Lengend Snippet: APS influences MAPK signaling pathways in ATO-induced BMSCs. Cells were exposed to 0.5 μmol/L ATO, and 0.5 μmol/L ATO + APS (20, 40, 100, and 200 μg/mL) for 48 h. (A) Western blotting analysis was applied to detect protein expressions of p-Jnk and Jnk, β -actin was used as a loading control, n = 3. (B) Western blotting analysis was conducted to detect protein expressions of p-p38 and p38, Gap was served as a loading control, n = 3. (C) Western blotting analysis was applied to detect protein expressions of p-Erk and Erk, β -actin was used as a loading control, n = 3. A two-tailed Student’s t -test was used to compare differences between two experimental groups. Error bars represent mean ± SEM. * P < 0.05, ** P < 0.01 vs control group, # P < 0.05 vs ATO group.

    Article Snippet: The membranes were then incubated with primary antibodies against B-cell lymphoma 2 (Bcl-2) (1:1 000, Proteintech, Chicago, USA, Cat. No. 68103-1-lg), Bcl-2-associated X protein (Bax) (1:1 000, Proteintech, Chicago, USA, Cat. No. 50599-2-lg), Caspase-3 (1:1 000, Proteintech, Chicago, USA, Cat. No. 19677-1-AP), cleaved Caspase-3 (1:2 000, Proteintech, Chicago, USA, Cat. No. 68773-1-lg), protein kinase B (Akt) (1:1 000, Cell signaling, Boston, USA, Cat. No. 9272) and phosphorylated-Akt (1:1 000, Cell signaling, Boston, USA, Cat. No. 4060), p53 (1:500, Gene Tex, California, USA, Cat. No. GTX70214), p16 (1:1 000, Proteintech, Chicago, USA, Cat. No.10883-1-AP), p38 mitogen-activated protein kinase (MAPK) (1:1 000, Proteintech, Chicago, USA, Cat. No.14064-1-AP), phosphorylated-p38 MAPK (1:1 000, Proteintech, Chicago, USA, Cat. No. 28796-1-AP), extracellular signal-regulated kinase (Erk) (1:2 000, Abcam, Cambridge, UK, Cat. No. ab184699), phosphorylated-Erk (1:2 000, Abcam, Cambridge, UK, Cat. No. ab201015), c-Jun N -terminal kinase (Jnk) (1:1 000, Proteintech, Chicago, USA, Cat. No.66210-1-lG), phosphorylated-Jnk (1:2 000, Abcam, Cambridge, UK, Cat. No. ab278538), GTPase-activating protein (Gap) (1:1 000, Abcam, Cambridge, UK, Cat. No. ab8245), and β -actin (1:1 000, Abcam, Cambridge, UK, Cat. No. ab8226) at 4 °C overnight.

    Techniques: Protein-Protein interactions, Western Blot, Control, Two Tailed Test