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OriGene Antibodies in recent publications
A common polymorphism in the LDL receptor gene has multiple effects on LDL receptor function Hum. Mol. Genet., Apr 2013; 22: 1424 - 1431. [anti-DDK]

Excitotoxicity Upregulates SARM1 Protein Expression and Promotes Wallerian-Like Degeneration of Retinal Ganglion Cells and Their Axons Invest. Ophthalmol. Vis. Sci., Apr 2013; 54: 2771 - 2780. [SARM1]

Modulation of TET2 expression and 5-methylcytosine oxidation by the CXXC domain protein IDAX Nature 497, 122-126 doi:10.1038/nature12052 [anti-DDK]

Natriuretic Peptide Receptor-3 Gene (NPR3): Nonsynonymous Polymorphism Results in Significant Reduction in Protein Expression Because of Accelerated Degradation Circ Cardiovasc Genet, Apr 2013; 6: 201 - 210. [NPR3]

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Home All anti-STAT5A antibodies

Anti-STAT5A TrueMAB Antibody clone 6D6

TrueMAB™ Antibodies - Made against Authentic Protein Antigens

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA502739
  • Purified STAT5A mouse monoclonal antibody, clone 6D6
  • FREE positive control: HEK293T cell transient overexpression lysate (LC418866) , 20ug
100ul $325 In Stock Add to Shopping Cart
CF502739
  • Carrier-free (BSA/glycerol-free) STAT5A mouse monoclonal antibody, clone 6D6
100ug $450 3-4 weeks Add to Shopping Cart
WB(1)
IHC(2)
IF(1)
FC(2)
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Also for STAT5A (NM_003152)
cDNA Clone shRNA/siRNA Lysate Protein Antibody
Gene NameHomo sapiens signal transducer and activator of transcription 5A (STAT5A)
Synonyms:MGF; STAT5
ImmunogenFull length human recombinant protein of human STAT5A (NP_003143) produced in HEK293T cell.
BufferPBS (PH 7.3) containing 1% BSA, 50% glycerol and 0.02% sodium azide.
Clone Nameclone 6D6 IsotypeIgG2b
Species ReactivityHuman Concentration0.5~1.0 mg/ml (Lot Dependent)
Purification Purified from mouse ascites fluids by affinity chromatography (Protein A or G Sepharose)
Guaranteed Application *WB, IHC, IF, FC Suggested DilutionsWB 1:2000, IHC 1:150, IF 1:100, FLOW 1:100
BackgroundThe protein encoded by this gene is a member of the STAT family of transcription factors. In response to cytokines and growth factors, STAT family members are phosphorylated by the receptor associated kinases, and then form homo- or heterodimers that translocate to the cell nucleus where they act as transcription activators. This protein is activated by, and mediates the responses of many cell ligands, such as IL2, IL3, IL7 GM-CSF, erythropoietin, thrombopoietin, and different growth hormones. Activation of this protein in myeloma and lymphoma associated with a TEL/JAK2 gene fusion is independent of cell stimulus and has been shown to be essential for the tumorigenesis. The mouse counterpart of this gene is found to induce the expression of BCL2L1/BCL-X(L), which suggests the antiapoptotic function of this gene in cells. [provided by RefSeq].
Related Pathway
Adipogenesis
EGFR1 Signaling Pathway
Jak-STAT signaling pathway

* Shipping is in business days
* OriGene provides validated application data and protocol, with money back guarantee.

WB Image
HEK293T cells were transfected with the pCMV6-ENTRY control (Left lane) or pCMV6-ENTRY STAT5A (RC205753, Right lane) cDNA for 48 hrs and lysed. Equivalent amounts of cell lysates (5 ug per lane) were separated by SDS-PAGE and immunoblotted with anti-STAT5A.
IHC Image
Immunohistochemical staining of paraffin-embedded Human lymph node tissue using anti-STAT5A mouse monoclonal antibody. (TA502739)
IHC Image
Immunohistochemical staining of paraffin-embedded Human lymphoma tissue using anti-STAT5A mouse monoclonal antibody. (TA502739)
IF Image
Anti-STAT5A mouse monoclonal antibody (TA502739) immunofluorescent staining of COS7 cells transiently transfected by pCMV6-ENTRY STAT5A(RC205753).
FC Image
Flow cytometric Analysis of Hela cells, using anti-STAT5A antibody(TA502739),(Red), compared to a nonspecific negative control antibody(TA50011),(Blue).
FC Image
Flow cytometric Analysis of Jurkat cells, using anti-STAT5A antibody(TA502739),(Red), compared to a nonspecific negative control antibody(TA50011),(Blue).

 

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