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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-MSH6 antibodies

Anti-MSH6 Antibody EPR3945

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Specifications Related Products Conjugation/Bulk FAQs
SKU Description Amount Price Availability*  
TA307745
  • Rabbit monoclonal antibody against MSH6(clone EPR3945)
  • FREE positive control: HEK293T cell transient overexpression lysate (LC424877) , 20ug
100ul $325 3-7 Days Add to Shopping Cart
WB(1)
IHC(1)
IF(1)
Gene NameHomo sapiens mutS homolog 6 (E. coli) (MSH6)
Synonyms:GTBP; HNPCC5; HSAP
ImmunogenA synthetic peptide corresponding to residues at the N-terminus in human MSH6 was used as an immunogen.
BufferStore at -20 C. Buffer: 50 mM Tris-Glycine (pH 7.4), 0.15 M NaCl, 40% Glycerol, 0.01% sodium azide and 0.05% BSA. Stable for 12 months from date of receipt.
Clone NameEPR3945 IsotypeRabbit IgG
Species ReactivityHuman, Mouse Concentration
Guaranteed Application *WB, IHC, IF Suggested DilutionsICC: 1: 100 - 250, IHC: 1: 100 - 250, IP: 1: 10 - 100, WB: 1:1,000-10,000,
BackgroundThe MutS homologue 6 protein (MSH6) is a member of the MutS homolog family required in the DNA mismatch repair system (1). MSH6 forms a MutS alpha dimer with MSH2, binding to DNA mismatches to initiate DNA repair (2). MutS alpha bends the DNA helix and recognizes single base mismatches and dinucleotide insertion-deletion loops in the DNA (2). Heterozygous mutations in the MSH6 gene are a cause of hereditary nonpolyposis colorectal cancer (HNPCC), forming a specific mispair binding complex with MSH3 (3, 4). The frequency of MSH6 mutation is higher in HNPCC than in atypical HNPCC (5). The MSH2/MSH6 dimer may also play a role in DNA homologous recombination repair (2).
Related Pathway

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

WB Image
Western blot analysis on (A) A431, (B) HeLa, and (C) SW480 cell lysates using anti-MSH6 RabMAb .
IHC Image
Immunohistochemical analysis of paraffin-embedded human colonic adenocarcinoma tissue using anti-MSH6 RabMAb .
IF Image
Immunofluorescent staining of HeLa cells using anti-MSH6 RabMAb .

 

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