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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-TEAD1 antibodies

Anti-TEAD1 Antibody EPR5279

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA311087
  • Rabbit Monoclonal antibody against TCF13 / TEF1 (TEAD1)
100ul $325 3-7 Days Add to Shopping Cart
WB(1)
FC(1)
Gene NameHomo sapiens TEA domain family member 1 (SV40 transcriptional enhancer factor) (TEAD1)
Synonyms:AA; NTEF-1; REF1; TCF-13; TCF13; TEAD-1; TEF-1
ImmunogenA synthetic peptide corresponding to residues on the C-terminus in human TCF13 / TEF1 was used as an immunogen.
BufferStore at -20 °C. Buffer: Antibody buffer, sodium azide, glycerol, and BSA. Stable for 12 months from date of receipt.
Clone NameEPR5279 Isotype
Species ReactivityHuman, Mouse, Rat Concentration
Guaranteed Application *WB, FC Suggested DilutionsWB: 1:10,000-50,000; ICC: 1:1000 - 5000;
BackgroundTCF13/TEF1 is a ubiquitous transcriptional enhancer factor that is a member of the TEA/ATTS domain family. This protein directs the transactivation of a wide variety of genes and, in placental cells, also acts as a transcriptional repressor (1). It plays a key role in the Hippo signaling pathway, a pathway involved in organ size control and tumor suppression by restricting proliferation and promoting apoptosis. TCF13/TEF1 binds specifically and cooperatively to the SPH and GT-IIC enhansons (2). It also binds M-CAT elements and regulates the development of cardiac, skeletal, and smooth muscles (3). Mutations in TCF13/TEF1 cause Sveinsson's chorioretinal atrophy (1).
Related Pathway

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* OriGene provides validated application data and protocol, with money back guarantee.

WB Image
Western blot analysis on (A) HeLa, (B) A673, (C) A431, (D) BxPC-3, and (E) JAR cell lysates using anti-TCF13 / TEF1 RabMAb.
FC Image
Flow cytometric analysis of permeabilized HeLa cells using anti-TCF13 / TEF1 RabMAb (red) or a rabbit IgG (negative) (green).

 

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