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首頁 /診斷試劑 /遺傳性基因標(biāo)準(zhǔn)品 /甲基丙二酸血癥 /MMUT c.729_730insTT Reference Standard

MMUT c.729_730insTT Reference Standard

CBPD0036

詢 價(jià)
索取COA
產(chǎn)品描述
產(chǎn)品數(shù)據(jù)庫
Introduction
Format Genomic DNA
Description Methylmalonic acidemia (MMA) is a lethal, severe heterogeneous disorder of methylmalonate and cobalamin (cbl; vitamin B12) metabolism with poor prognosis. Two main forms of the disease have been identified, isolated methylmalonic acidurias and combined methylmalonic aciduria and homocystinuria, which is respectively caused by different gene mutations. 
   
Technical Data
Gene MMUT
DNA Change NM_000255.4:c.729_730insTT
AA Change p.Asp244fs
Zygosity Heterozygous
Allelic Frequency 50%
Chr position (GRCh37) Chr6: 49425428 - 49425429 insTT
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 Download for COA
Storage 2-8°C
Expiry 36 months from the date of manufacture

藥靶模型聯(lián)系方式: 華東銷售經(jīng)理:18240630236 全國銷售經(jīng)理:18066071954
診斷標(biāo)準(zhǔn)品聯(lián)系方式: 華東銷售經(jīng)理:15000320447 華北銷售經(jīng)理:18131625521 華南銷售經(jīng)理:13484295986 華中&西南銷售經(jīng)理:13871580511 全國銷售經(jīng)理:13484295986

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