p38β Antibody (YA5003)
(Synonyms: MAPK11; PRKM11; SAPK2; SAPK2B; Mitogen-activated protein kinase 11; MAP kinase 11; MAPK 11; Mitogen-activated protein kinase p38 beta; MAP kinase p38 beta; p38b; Stress-activated protein kinase 2b; SAPK2b; p38-2)p38β Antibody (YA5003) is a Mouse-derived and non-conjugated monoclonal antibody, targeting to p38β.
-
Host:
Mouse
-
Application:
WB, ELISA
-
Reactivity :
Human
-
Formulation:
Supplied in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
-
Conjugation:
Non-conjugated
Applications
| Application |
WB
WB: Western Blot
|
ELISA
ELISA: Enzyme Linked Immunosorbent Assay
|
|---|---|---|
| Dilution Ratio | 1:500-1:2000 | 1:10000 |
Product Details
p38β Antibody (YA5003) is a Mouse-derived and non-conjugated monoclonal antibody, targeting to p38β.
-
Host Mouse
-
Clonality Monoclonal
-
Species ReactivityHuman
-
Calculated Molecular Weight Predicted band size: 41 kDa;
Purified recombinant fragment of p38β (aa251-363) expressed in E. Coli.
affinity purified.
Non-conjugated
Unmodified
Product Properties
-
Appearance
Solution
-
Formulation
Supplied in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
-
Storage & Stability
Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles.
-
Shipping
Shipping with blue ice.
Background
-
Function
p38β (MAPK11) is a stress-activated serine/threonine MAPK within the p38α, p38β, p38γ, and p38δ family, which transduces extracellular stress signals into cellular adaptation and survival responses[1]. Mechanistically, p38β belongs to the broader p38 MAPK pathway involved in inflammation, stress response, transcription, growth, differentiation, motility, and survival[1]. In endothelial cells, SOCE activates CaMKKβ-AMPKα1-p38β MAPK signaling, and p38β phosphorylates STIM1 to suppress store-operated Ca2+ entry and permeability responses[2]. In disease models, SARS-CoV-2 requires p38β as a critical host factor for viral replication after viral mRNA expression, supporting p38β-focused antiviral research[3]. Compared with p38α, p38β shows distinct functional relevance because SARS-CoV-2 proviral activity was reported for p38β but not shared with p38α[3]. The isoform distinction also matters for inhibitor design because p38α/MAPK14 is described as the major proinflammatory member, whereas p38β/MAPK11 is treated as a noninflammatory isoform in substrate-selective inhibitor development[4]. For experimental applications, p38 catalytic inhibitors such as SB203580 lack isoform specificity, limiting interpretation of p38β biology in complex disease models[1][4]. Therefore, p38β research benefits from isoform-aware genetic depletion, phosphoproteomics, and selective inhibitor strategies that separate p38β-dependent biology from p38α-driven inflammatory signaling[3][4].
-
Subcellular Localization
Cytoplasm; Nucleus
-
Expression
Tissue_specificity:It is found in the highest concentrations in the brain and heart. It is also expressed in the placenta, lungs, liver, skeletal muscle, kidneys, and pancreas. -
Isoforms & Post-Translational Modification
Q15759 has 2 isomers: Q15759-1: 41357 Da (predicted); Q15759-3: 23603 Da (predicted).
Dually phosphorylated on Thr-180 and Tyr-182 by MAP2K3/MKK3, MAP2K4/MKK4 and MAP2K6/MKK6, which activates the enzyme -
Subunit
Interacts with HDAC3 and DUSP16
-
SwissProt ID
-
Synonyms
MAPK11; PRKM11; SAPK2; SAPK2B; Mitogen-activated protein kinase 11; MAP kinase 11; MAPK 11; Mitogen-activated protein kinase p38 beta; MAP kinase p38 beta; p38b; Stress-activated protein kinase 2b; SAPK2b; p38-2
Documentation
[1]. Martin ED, et al. p38 MAPK in cardioprotection - are we there yet? Br J Pharmacol. 2015 Apr;172(8):2101-13. [Content Brief]
[2]. Sundivakkam PC, et al. Store-operated Ca2+ entry (SOCE) induced by protease-activated receptor-1 mediates STIM1 protein phosphorylation to inhibit SOCE in endothelial cells through AMP-activated protein kinase and p38β mitogen-activated protein kinase. J Biol Chem. 2013 Jun 7;288(23):17030-17041. [Content Brief]
[3]. Higgins CA, et al. SARS-CoV-2 hijacks p38β/MAPK11 to promote virus replication. mBio. 2023 Aug 31;14(4):e0100723. [Content Brief]
[4]. Shah NG, et al. Novel Noncatalytic Substrate-Selective p38α-Specific MAPK Inhibitors with Endothelial-Stabilizing and Anti-Inflammatory Activity. J Immunol. 2017 Apr 15;198(8):3296-3306. [Content Brief]