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首頁(yè) /診斷試劑 /腫瘤標(biāo)準(zhǔn)品 /Mutation /MSH6 p.Y1066* Reference Standard

MSH6 p.Y1066* Reference Standard

CBP10592

詢 價(jià)
索取COA
產(chǎn)品描述
產(chǎn)品數(shù)據(jù)庫(kù)
Introduction 
Format Genomic DNA
Description MSH6, mutS homolog 6, binds with Msh2 to form the MutS-alpha complex, which functions in initiation of the DNA mismatch repair system and is associated with microsatellite instability (MSI). Mutations in MSH6 are associated with susceptibility to colon cancer and endometrial cancer, and germline MSH6 mutations are associated with Lynch (Hereditary Nonpolyposis Colorectal Cancer) syndrome.
   
Technical Data 
DNA Change c.3198_3199del
AA Change p.Y1066*
Mutation type Frame_Shift_Del
Zygosity N/A
Allelic Frequency N/A
Transcript NM_000179.3
Cosmic ID N/A
Chr position(GRCh37) chr2-48030582-TA-
Buffer Tris-EDTA
   
Product Information 
Intended Use Research Use Only
Unit Size 1ug
Concentration Download for COA
Purofication Download for COA
DNA electrophoresis Download for COA
Sanger sequencing
Storage 2-8℃
Expiry 36 months from the date of manufacture

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