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Purified Mouse Anti-Stat2 (pY690)
Purified Mouse Anti-Stat2 (pY690)
Western Blot analysis of Stat2 (pY690) in human histiocytic lymphoma. Lysates from control (left panel) and Interferon-α-activated (right panel) U937 cells (ATCC CRL-1593.2) was probed with Mouse anti-Stat2 (pY690) monoclonal antibody at concentrations of 0.5 µg/ml, (lanes 1, 4), 0.25 µg/ml, (lanes 2, 5) and 0.125 µg/ml (lanes 3, 6), respectively).  Stat2 (pY690) is identified as a band of 113 kDa in the treated cells.
Western Blot analysis of Stat2 (pY690) in human histiocytic lymphoma. Lysates from control (left panel) and Interferon-α-activated (right panel) U937 cells (ATCC CRL-1593.2) was probed with Mouse anti-Stat2 (pY690) monoclonal antibody at concentrations of 0.5 µg/ml, (lanes 1, 4), 0.25 µg/ml, (lanes 2, 5) and 0.125 µg/ml (lanes 3, 6), respectively).  Stat2 (pY690) is identified as a band of 113 kDa in the treated cells.
Product Details
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BD Pharmingen™
Human (QC Testing)
Mouse IgG1, κ
Phosphorylated Human Stat2 Peptide
Western blot (Routinely Tested)
113 kDa
0.5 mg/ml
AB_397021
Aqueous buffered solution containing ≤0.09% sodium azide.
RUO


Preparation And Storage

The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography. Store undiluted at 4°C.

Product Notices

  1. Since applications vary, each investigator should titrate the reagent to obtain optimal results.
  2. Please refer to www.bdbiosciences.com/us/s/resources for technical protocols.
  3. 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.
558095 Rev. 5
Antibody Details
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7a/Stat2

Stat (Signal transducer and activators of transcription) proteins are critical mediators of the biologic activity of cytokines, including interleukins, interferons, erythropoietin, and growth factors.  Ligand-receptor interaction leads to activation of constitutively associated JAK family kinases and subsequent recruitment/activation of Stat proteins by tyrosine phosphorylation.  Active Stat proteins then move to the nucleus to promote transcription of cytokine-inducible genes.  Seven Stat proteins have been cloned, each of which is differentially expressed and/or activated in a cytokine-specific and cell type-specific manner.  Stat1 and Stat2 are components of the ISGF3 (Interferon-Stimulated Gene Factor 3) complex, which is the primary transcription activator induced by the binding of the interferon to a specific cell-surface receptor.  Stat2 is a 113-kDa protein having approximately 40% homology with Stat1α.  Stat2 interacts with Stat1 for the efficient activation of Stat1 in response to IFN-α, which is essential for normal transcriptional activity of the ISGF3 complex.  Stat2 phosphorylation at the tyrosine 690 residue (Y690) after IFN-α activation can occur independently of Stat1, but the localization and nuclear stability of phosphorylated Stat2 is dependent on Stat1.

The 7a/Stat2 monoclonal antibody recognizes the phosphorylated Y690 of human Stat2.

558095 Rev. 5
Format Details
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Purified
Tissue culture supernatant is purified by either protein A/G or affinity purification methods. Both methods yield antibody in solution that is free of most other soluble proteins, lipids, etc. This format provides pure antibody that is suitable for a number of downstream applications including: secondary labeling for flow cytometry or microscopy, ELISA, Western blot, etc.
Purified
558095 Rev.5
Citations & References
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Development References (2)

  1. Bromberg J, Darnell JE. The role of STATs in transcriptional control and their impact on cellular function. Oncogene. 2000; 19(21):2468-2473. (Biology). View Reference
  2. Heim MH. The Jak-STAT pathway: specific signal transduction from the cell membrane to the nucleus. Eur J Clin Invest. 1996; 26(1):1-12. (Biology). View Reference
558095 Rev. 5

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Comparisons, where applicable, are made against older BD Technology, manual methods or are general performance claims.  Comparisons are not made against non-BD technologies, unless otherwise noted.

For Research Use Only. Not for use in diagnostic or therapeutic procedures.