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

CBPD0027

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產(chǎn)品描述

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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

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藥靶模型聯(lián)系方式: 華東銷售經(jīng)理(上海）：18240630236 華東銷售經(jīng)理(上海、江蘇、安徽）：15715191010 華北銷售經(jīng)理：18628311252 華南銷售經(jīng)理：13823536064 華中&華西銷售經(jīng)理：18071545918 華中&西南銷售經(jīng)理：13871580511 全國銷售經(jīng)理：13816461235
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AI-Edigene? SLC26A4 IVS7-2A>G Reference Standard Plus