Product Pathways - Jak/Stat Pathway
Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb (Sepharose Bead Conjugate) #5167
|5167S||400 µl (40 immunoprecipitations)||---||In Stock||---|
|5167||carrier free and custom formulation / quantity||email request|
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|IP||1:20||Human, Mouse||Endogenous||84, 91||Rabbit IgG|
Species cross-reactivity is determined by western blot using the unconjugated antibody.
Applications Key: IP=Immunoprecipitation
Specificity / Sensitivity
Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb (Sepharose Bead Conjugate) detects endogenous levels of Stat1 only when phosphorylated at Tyr701. The antibody detects phosphorylated Tyr701 of p91 Stat1 and also the p84 splice variant. This antibody does not cross-react with the corresponding phospho-tyrosines of other Stat proteins.
Source / Purification
Monoclonal antibody is produced by immunizing animals with a synthetic phosphopeptide corresponding to residues surrounding Tyr701 of human Stat1.
Immunoprecipitation of HeLa cell lysates, untreated or treated with interferon-α (IFN-α), using Rabbit (DA1E) IgG mAb XP® Isotype Control (Sepharose Bead Conjugate) #3423 (Lanes 1 and 2) and Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb (Sepharose Bead Conjugate) (Lanes 3 and 4). The blot was probed using Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb #9167.
This Cell Signaling Technology antibody is immobilized via covalent binding of primary amino groups to N-hydroxysuccinimide (NHS)-activated sepharose beads. Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb (Sepharose Bead Conjugate) is useful for the immunoprecipitation of Stat1 phosphorylated at Tyr701. The antibody is expected to exhibit the same species cross-reactivity as the unconjugated Phospho-Stat1 (Tyr701) (58D6) Rabbit mAb #9167.
The Stat1 transcription factor is activated in response to a large number of ligands (1) and is essential for responsiveness to IFN-α and IFN-γ (2,3). Phosphorylation of Stat1 at Tyr701 induces Stat1 dimerization, nuclear translocation, and DNA binding (4). Stat1 protein exists as a pair of isoforms, Stat1α (91 kDa) and the splice variant Stat1β (84 kDa). In most cells, both isoforms are activated by IFN-α, but only Stat1α is activated by IFN-γ. The inappropriate activation of Stat1 occurs in many tumors (5). In addition to tyrosine phosphorylation, Stat1 is also phosphorylated at Ser727 through a p38 mitogen-activated protein kinase (MAPK)-dependent pathway in response to IFN-α and other cellular stresses (6). Serine phosphorylation may be required for the maximal induction of Stat1-mediated gene activation.
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For Research Use Only. Not For Use In Diagnostic Procedures.
Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.
This antibody is developed, validated, and produced by CST using in part technology under license (granting certain rights including those under U.S. Patents No. 5,675,063 and 7,429,487) from Epitomics, Inc.