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BD Pharmingen™ Purified Mouse Anti-MEK1 (pS298)
Clone J114-64 (RUO)
Western blot analysis of MEK1 (pS298) in mouse embryonic fibroblasts. Lysates from detached (trypsinized, lanes 1-3) and attached (80-90% confluent, lanes 4-6) NIH/3T3 cell line were probed with purified mouse anti-MEK1 (pS298) monoclonal antibody at concentrations of 0.015 (lanes 1 and 4), 0.008 (lanes 2 and 5), and 0.004 µg/ml (lanes 3 and 6). MEK1 (pS298) is identified as a band of 45 kDa in the treated cells.
Western blot analysis of MEK1 (pS298) in mouse embryonic fibroblasts. Lysates from detached (trypsinized, lanes 1-3) and attached (80-90% confluent, lanes 4-6) NIH/3T3 cell line were probed with purified mouse anti-MEK1 (pS298) monoclonal antibody at concentrations of 0.015 (lanes 1 and 4), 0.008 (lanes 2 and 5), and 0.004 µg/ml (lanes 3 and 6). MEK1 (pS298) is identified as a band of 45 kDa in the treated cells.
Western blot analysis of MEK1 (pS298) in mouse embryonic fibroblasts. Lysates from detached (trypsinized, lanes 1-3) and attached (80-90% confluent, lanes 4-6) NIH/3T3 cell line were probed with purified mouse anti-MEK1 (pS298) monoclonal antibody at concentrations of 0.015 (lanes 1 and 4), 0.008 (lanes 2 and 5), and 0.004 µg/ml (lanes 3 and 6). MEK1 (pS298) is identified as a band of 45 kDa in the treated cells.
Regulatory Status Legend
Any use of products other than the permitted use without the express written authorization of Becton, Dickinson and Company is strictly prohibited.
Preparation And Storage
Product Notices
- Since applications vary, each investigator should titrate the reagent to obtain optimal results.
- Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
- Caution: Sodium azide yields highly toxic hydrazoic acid under acidic conditions. Dilute azide compounds in running water before discarding to avoid accumulation of potentially explosive deposits in plumbing.
MEK (Map/Erk Kinase) 1 and 2 are serine/threonine kinases, also known as MAP kinase kinases (MAP2K1 and 2, MAPKK1 and 2, or MKK1 and 2). They activate the MAP (Mitogen-Activated Protein) kinases, also known as ERKs (Extracellular signal Regulated Kinases), which are critical kinases in multiple signal transduction pathways that regulate cell growth and differentiation. Activation of MEK 1 and 2 is dependent upon phosphorylation of serines 218 and/or 222 by activated MAP kinase kinase kinases (MAP3Ks), such as the Raf isoforms. Hormones, growth and differentiating factors, or tumor promoters induce Raf activation via activation of Ras proteins. Alternatively, cellular adhesion can lead to phosphorylation of MEK1 at serine 298 (S298), mediated by p21-activated kinase (PAK). The S298-phosphorylated MEK1 has an enhanced capacity to interact with Raf, resulting in MEK1 activation.
The J114-64 monoclonal antibody recognizes the phosphorylated S298 of MEK1.
Development References (3)
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Eblen ST, Slack JK, Weber MJ, Catling AD. Rac-PAK signaling stimulates extracellular signal-regulated kinase (ERK) activation by regulating formation of MEK1-ERK complexes. Mol Cell Biol. 2002; 22(17):6023-6033. (Biology).
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Kolch W. Meaningful relationships: the regulation of the Ras/Raf/MEK/ERK pathway by protein interactions. Biochem J. 2000; 351:289-305. (Biology). View Reference
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Slack-Davis JK, Eblen ST, Zecevic M, et al. PAK1 phosphorylation of MEK1 regulates fibronectin-stimulated MAPK activation. J Cell Biol. 2003; 162(2):281-291. (Biology).
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For Research Use Only. Not for use in diagnostic or therapeutic procedures.