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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-OTX2 antibodies

Anti-OTX2 Antibody EPR3347

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA307062
  • Rabbit monoclonal antibody against OTX2(clone EPR3347)
  • FREE positive control: HEK293T cell transient overexpression lysate (LC411946) , 20ug
100ul $325 3-7 Days Add to Shopping Cart
WB(1)
IHC(1)
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Also for OTX2 (NM_021728)
cDNA Clone shRNA/siRNA Lysate Protein Antibody
Gene NameHomo sapiens orthodenticle homeobox 2 (OTX2), transcript variant 1
Synonyms:CPHD6; MCOPS5
ImmunogenA synthetic peptide corresponding to residues in human OTX2 was used as an immunogen. This antibody is predicted to cross-react with OTX1 based on sequence analysis.
Buffer50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA.
Clone NameEPR3347 IsotypeRabbit IgG
Species ReactivityHuman Concentration
Guaranteed Application *WB, IHC Suggested DilutionsIHC: 1:100 - 250, WB: 1:1,000 - 10,000,
BackgroundHomeobox protein OTX2 is a member of the bicoid sub-family of homeodomain-containing transcription factors. It acts as a transcription factor and is reported to play a role in brain and sensory organ development (1); more specifically, forebrain and eye development (2). The OTX2 is required to determine mesencephalic versus metencephalic (cerebellum/pons) territory during embryogenesis. This function of OTX2 primarily involves positioning and maintaining the mid-hindbrain organizer at the border between midbrain and anterior hindbrain (3). OTX2 is expressed during development in the neuroepithelium of most of the forebrain and midbrain, including the eye domain. In mice, complete elimination of the OTX2 function results in the absence of the forebrain and embryonic lethality (4). Defects in OTX2 are the caused of microphthalmia syndromic type 5, a clinically heterogeneous disorder of the eye formation (5).
Related Pathway

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WB Image
Western blot analysis on Y79 cell lysate using anti-OTX2 RabMAb .
IHC Image
Immunohistochemical analysis of paraffin-embedded human fetal brain tissue using anti-OTX2 RabMAb .

 

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