首页 /诊断试剂 /遗传性基因标准品 /遗传性耳聋 /AI-Edigene® SLC26A4 IVS7-2A>G Reference Standard Plus

AI-Edigene® SLC26A4 IVS7-2A>G Reference Standard Plus

CBPD0027

询价

索取COA

产品描述

产品数据库

Introduction
Format	Genomic DNA
Description	SLC26A4 (Solute Carrier Family 26 Member 4) is a Protein Coding gene. Diseases associated with SLC26A4 include Pendred Syndrome and Deafness, Autosomal Recessive 4, With Enlarged Vestibular Aqueduct. Among its related pathways are Transport of inorganic cations/anions and amino acids/oligopeptides and Disorders of transmembrane transporters.

Technical Data
DNA Change	IVS7-2A>G
AA Change	N/A
Zygosity	Homozygous
Allelic Frequency	100%
Chr position (GRCh38)	chr7: 107683453
Transcript	NM_000441.2
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

相关产品推荐

• AI-Edigene® GJB3 p.E183K Reference Standard Plus • AI-Edigene® GJB3 p.R180* 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.G12Vfs*2/p.M34T double mutation 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：ChrMT_1494 m.1494C>T Reference Standard

下一篇：AI-Edigene® SLC26A4 p.H723R Reference Standard Plus

返回列表

药靶模型联系方式: 华东销售经理：18240630236 全国销售经理：18066071954
诊断标准品联系方式：华东销售经理：15000320447 华北销售经理：18131625521 华南销售经理：13484295986 华中&西南销售经理：13871580511 全国销售经理：13484295986

扫二维码