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p38 alpha (MAP Kinase) Antibody, Clone 9F12: FITC
Mouse Anti-Human p38 alpha (MAP Kinase) Monoclonal IgG1
Artikelnummer
STRSMC-152D-FITC
Verpackungseinheit
100 µg
Hersteller
Stressmarq Biosciences
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Target: p38 MAPK
Conjugate: FITC
Product Type: Monoclonal
Clone Number: 9F12
Immunogen: Full length recombinant protein expressed in E.coli cells
Swiss-Prot: Q16539
Purification: Protein G Purified
Storage Buffer: PBS, 50% glycerol, 0.09% sodium azide *Storage buffer may change when conjugated
Concentration: 1 mg/ml
Specificity: Detects ~38kDa.
Cellular Localization: Cytoplasm,Nucleus
Scientific Background: The MAPK (mitogen activated protein kinase) comprises a family of ubiquitous praline-directed, proteinserine/ threonine kinases which signal transduction pathways that control intracellular events including acute responses to hormones and major developmental changes in organisms (1). This super family consists of stress activated protein kinases (SAPKs); extracellular signal-regulated kinases (ERKs); and p38 kinases, each of which forms a separate pathway (2). The kinase members that populate each pathway are sequentially activated by phosphorylation. Upon activation, p38 MAPK/SAPK2α translocates into the nucleus where it phosphorylates one or more nuclear substrates, effecting transcriptional changes and other cellular processes involved in cell growth, division, differentiation, inflammation, and death (3). Specifically p38 always acts as a pro-apoptotic factor with its activation leading to the release of cytochrome c from mitochondria and cleavage of caspase 3 and its downstream effector, PARP (4). p38 MAPK is activated by a variety of chemical stress inducers including hydrogen peroxide, heavy metals, anisomycin, sodium salicylate, LPS, and biological stress signals such as tumor necrosis factor, interleukin-1, ionizing and UV irradiation, hyperosmotic stress and chemotherapeutic drugs (5). As a result, p38 alpha has been widely validated as a target for inflammatory disease including rheumatoid arthritis, COPD and psoriasis (6) and has also been implicated in cancer, CNS and diabetes (7).
References: 1. Pearson, G. et al (2001). Endocrine Reviews 22 (2): 153-183.2. Fan, Y. et al (2007) Mol. Cells 23 (1): 30-38.3. Han, J. et al. (1994) Science 265: 808-811.4. Van, L. A., et al. (2004) Faseb J. 18: 1946−1948.5. Deng et al. (2003) Cell. 115: 61-70.6. Salojin KV, et al. (2006) J Immunol. 176 (3):1899-907.7. Medicherla S. et al. (2006). J Pharmacol Exp Ther.318(1): 99-107.
Field of Use: Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
Conjugate: FITC
Product Type: Monoclonal
Clone Number: 9F12
Immunogen: Full length recombinant protein expressed in E.coli cells
Swiss-Prot: Q16539
Purification: Protein G Purified
Storage Buffer: PBS, 50% glycerol, 0.09% sodium azide *Storage buffer may change when conjugated
Concentration: 1 mg/ml
Specificity: Detects ~38kDa.
Cellular Localization: Cytoplasm,Nucleus
Scientific Background: The MAPK (mitogen activated protein kinase) comprises a family of ubiquitous praline-directed, proteinserine/ threonine kinases which signal transduction pathways that control intracellular events including acute responses to hormones and major developmental changes in organisms (1). This super family consists of stress activated protein kinases (SAPKs); extracellular signal-regulated kinases (ERKs); and p38 kinases, each of which forms a separate pathway (2). The kinase members that populate each pathway are sequentially activated by phosphorylation. Upon activation, p38 MAPK/SAPK2α translocates into the nucleus where it phosphorylates one or more nuclear substrates, effecting transcriptional changes and other cellular processes involved in cell growth, division, differentiation, inflammation, and death (3). Specifically p38 always acts as a pro-apoptotic factor with its activation leading to the release of cytochrome c from mitochondria and cleavage of caspase 3 and its downstream effector, PARP (4). p38 MAPK is activated by a variety of chemical stress inducers including hydrogen peroxide, heavy metals, anisomycin, sodium salicylate, LPS, and biological stress signals such as tumor necrosis factor, interleukin-1, ionizing and UV irradiation, hyperosmotic stress and chemotherapeutic drugs (5). As a result, p38 alpha has been widely validated as a target for inflammatory disease including rheumatoid arthritis, COPD and psoriasis (6) and has also been implicated in cancer, CNS and diabetes (7).
References: 1. Pearson, G. et al (2001). Endocrine Reviews 22 (2): 153-183.2. Fan, Y. et al (2007) Mol. Cells 23 (1): 30-38.3. Han, J. et al. (1994) Science 265: 808-811.4. Van, L. A., et al. (2004) Faseb J. 18: 1946−1948.5. Deng et al. (2003) Cell. 115: 61-70.6. Salojin KV, et al. (2006) J Immunol. 176 (3):1899-907.7. Medicherla S. et al. (2006). J Pharmacol Exp Ther.318(1): 99-107.
Field of Use: Not for use in humans. Not for use in diagnostics or therapeutics. For in vitro research use only.
| Artikelnummer | STRSMC-152D-FITC |
|---|---|
| Hersteller | Stressmarq Biosciences |
| Hersteller Artikelnummer | SMC-152D-FITC |
| Green Labware | Nein |
| Verpackungseinheit | 100 µg |
| Mengeneinheit | STK |
| Reaktivität | Human, Mouse (Murine), Rat (Rattus) |
| Klonalität | Monoclonal |
| Methode | Immunoprecipitation, Western Blotting, ELISA, Immunohistochemistry |
| Isotyp | IgG1 |
| Human Gene ID | 1432 |
| Wirt | Mouse |
| Produktinformation (PDF) | Download |
| MSDS (PDF) | Download |
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