GJB2 p.M34T Reference Standard

CBPD0024

詢(xún) 價(jià)

索取COA

產(chǎn)品描述

產(chǎn)品數據庫

Introduction
Format	Genomic DNA
Description	Genetic deafness is a hearing disorder caused by genetic mutations. It is mainly caused by the mutation of mutations in genetic deaf genes and is inherited to descendants. Common deaf genes include GJB2, GJB3, SLC26A4, mitochondrial 12S RRNA, etc.

Technical Data
DNA Change	c.101T>C
AA Change	p.M34T
Zygosity	Heterozygous
Allelic Frequency	50%
Chr position (GRCh37)	chr13-20763620
Transcript	NM_004004.6
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°C
Expiry	36 months from the date of manufacture

相關(guān)產(chǎn)品推薦

? AI-Edigene? GJB3 p.E183K Reference Standard Plus ? AI-Edigene? GJB3 p.R180* Reference Standard Plus ? AI-Edigene? SLC26A4 IVS7-2A>G Reference Standard Plus ? AI-Edigene? SLC26A4 p.H723R Reference Standard Plus ? ChrMT_ m.1555 A>G Reference Standard ? ChrMT_1494 m.1494C>T Reference Standard ? GJB2 p.E120del/p.M195I double mutation Reference Standard ? GJB2 p.G12Vfs*2 Reference Standard ? GJB2 p.G12Vfs*2/p.M34T double mutation Reference Standard ? GJB2 p.G4D Reference Standard

上一篇：AI-Edigene? GJB3 p.E183K Reference Standard Plus

下一篇：GJB2 p.G4D Reference Standard

返回列表

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

掃二維碼

立即提交

毛片免费毛片一级jjj毛片,日本在线亚州精品视频在线,国产精品国偷自产在线,久久精品色,日韩精品免费电影,欧美综合国产精品日韩一,国产六区

GJB2 p.M34T Reference Standard