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首頁(yè) /診斷試劑 /遺傳性基因標(biāo)準(zhǔn)品 /甲基丙二酸血癥 /MMAA c.503del Reference Standard

MMAA c.503del Reference Standard

CBPD0032

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 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 MMAA
DNA Change NM_172250.3:c.503delC
AA Change p.Thr168fs
Zygosity Heterozygous
Allelic Frequency 50%
Chr position (GRCh37) Chr4: 146563578 delC
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

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診斷標(biāo)準(zhǔn)品聯(lián)系方式: 華東銷(xiāo)售經(jīng)理:15000320447 華北銷(xiāo)售經(jīng)理:18628311252 華中&華西銷(xiāo)售經(jīng)理:18071545918 華中&西南銷(xiāo)售經(jīng)理:13871580511 全國(guó)銷(xiāo)售經(jīng)理:13816461235

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