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- mouse monoclonal IgG1; 200 µg/ml
- recommended for detection of Stat1α p91 and Stat1β p84 of mouse, rat and human origin phosphorylated at Tyr 701 by WB, IP, IF, FCM and ELISA
- TransCruz reagent for Gel Supershift and ChIP applications, sc-8394 X, 200 µg/0.1 ml
- fluorescein (sc-8394 FITC), phycoerythrin (sc-8394 PE), PerCP (sc-8394 PerCP) and PerCP-Cy5.5 (sc-8394 PCPC5) conjugate for intracellular FCM, 100 tests
- for phosphorylation positive (sc-2222) and non-activated control (sc-2200) cell extract
- blocking peptide, sc-8394 P
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Stat1 Background Information Membrane receptor signaling by various ligands, including interferons and growth hormones such as EGF, induces activation of Jak kinases which then leads to tyrosine phosphorylation of the various Stat transcription factors (1,2). Stat1 and Stat2 are induced by IFN-a and form a heterodimer which is part of the ISGF3 transcription factor complex (3). Although early reports indicate Stat3 activation by EGF and IL-6, it has been shown that Stat3∫ appears to be activated by both while Stat3å is activated by EGF, but not by IL-6 (4,5). Highest expression of Stat4 is seen in testis and myeloid cells (6). IL-12 has been identified as an activator of Stat4 (2). Stat5 has been shown to be activated by prolactin and by IL-3 (7). Stat6 is involved in IL-4 activated signaling pathways (8).
| p-Stat1 (A-2) Product Citations |
See how others have used p-Stat1 (A-2): sc-8394 antibody and or p-Stat1 (A-2) antibody conjugates.
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p-Stat1 (A-2)
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Western blot analysis of Stat1 activation in untreated (A,C) and γ-interferon-induced (B,D) HeLa cells. Antibodies tested include a phospho-specific Stat1 monoclonal, p-Stat1 (A-2): sc-8394 (A,B) and a control antibody, Stat1α p91 (C-111): sc-417 (C,D).
p-Stat1 (A-2) PE: sc-8394 PE. Intracellular FCM analysis of fixed and permeabilized control (green line histogram) and IFN-γ-induced (solid orange histogram) U-937 cells. Dotted pink histogram represents the isotype control, normal mouse IgG 1: sc-2866.
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