Phospho-p38 alpha (T180/Y182) Surveyor IC

Discontinued Product

SUV869B has been discontinued.
View all p38 alpha products.
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Citations (2)
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Phospho-p38 alpha (T180/Y182) Surveyor IC Summary

Specifications

Source
N/A
Shipping Conditions
The product is shipped at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
Storage
Store the unopened product at 2 - 8 °C. Do not use past expiration date.
Species
Human Mouse Rat

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Background: p38 alpha

The p38 Mitogen-activated Protein Kinases (MAPKs) are a family of four related Ser/Thr kinases activated by proinflammatory cytokines and environmental stresses. All four p38 family members, alpha, beta, gamma, and delta, are phosphorylated by MKK3 and/or MKK6 at dual Thr and Tyr positions within the phosphoacceptor sequence Thr-Gly-Tyr. Once activated, p38 phosphorylates a number of targets, including the nuclear transcription factors ATF2 and Max.

The most frequently analyzed family member, p38 alpha, also known as SAPK2a and MAPK14, was initially purified as a kinase critical to the signaling cascade linking IL-1 to MAPKAPK-2 and the small heat shock protein HSP27. Ubiquitously expressed, p38 alpha is dually phosphorylated by MKK3 and MKK6 at Thr180 and Tyr182. Once activated, p38 alpha phosphorylates a number of targets, including the cytoplasmic kinases MNK 4 and PRAK5 and the nuclear transcription factors ATF2 1 and STAT1. Several promising compounds that inhibit p38 alpha are being investigated as potential therapies for arthritic and inflammatory diseases.

Entrez Gene IDs
1432 (Human); 26416 (Mouse); 81649 (Rat)
Alternate Names
CSBP;CSBP1;CSBP2;CSPB1;EXIP;MAPK14;Mitogen-activated protein kinase;Mitogen-activated protein kinase 14;Mxi2;p38;p38ALPHA;PRKM14;PRKM15;RK;SAPK2A; MAPK14; p38 alpha; SAPK2a

Citations for Phospho-p38 alpha (T180/Y182) Surveyor IC

R&D Systems personnel manually curate a database that contains references using R&D Systems products. The data collected includes not only links to publications in PubMed, but also provides information about sample types, species, and experimental conditions.

2 Citations: Showing 1 - 2
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  1. Immunomodulation of nasal epithelial cells by Staphylococcus aureus-derived serine proteases.
    Authors: Rudack C, Sachse F, Albert N, Becker K, von Eiff C
    J. Immunol., 2009-11-16;183(11):7592-601.  2009-11-16
  2. Gene transfer to interfere with TNFalpha signaling in neuropathic pain.
    Authors: Hao S, Mata M, Glorioso JC, Fink DJ
    Gene Ther., 2007-04-19;14(13):1010-6.  2007-04-19

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