GJB2 p.G12Vfs*2/p.M34T double mutation Reference Standard

CBPD0022

詢價(jià)

索取COA

產(chǎn)品描述

產(chǎn)品數(shù)據(jù)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
Mutation 1	DNA Change: c.35delG
	AA Change: p.G12Vfs*2
	Chr position(GRCh37): chr13-20763686-C-
	Zygosity: Heterozygous
	Allelic Frequency: 50%
Mutation 2	DNA Change: c.101T>C
	AA Change: p.M34T
	Chr position(GRCh37): chr13-20763620-A-G
	Zygosity: Heterozygous
	Allelic Frequency: 50%
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	Figure 1. GJB2 p.G12Vfs*2 Figure 2. GJB2 p.M34T
Storage	4°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_1494 m.1494C>T Reference Standard ? GJB2 p.E120del/p.M195I double mutation Reference Standard ? GJB2 p.G12Vfs*2 Reference Standard ? GJB2 p.G4D Reference Standard ? GJB2 p.L79Cfs*3/p.G59Afs*18 double mutation Reference Standard ? GJB2 p.M34T Reference Standard

上一篇：GJB2 p.G4D Reference Standard

下一篇：GJB2 p.G12Vfs*2 Reference Standard

返回列表

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

掃二維碼

立即提交

亚洲无线乱码高清在线观看一区,色一级,精品伊人久久,2018国产大陆天天弄,狠狠操夜夜爱,欧美日韩中文字幕在线,日本人视频网站一

GJB2 p.G12Vfs*2/p.M34T double mutation Reference Standard