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α-thalassemia αα/--SEA Reference Standard

CBPD0029

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产品描述

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Introduction
Format	Genomic DNA
Description	a-thalassemia is the most common human monogenic hereditary diseases in theworld. Generally, a-thalassemia is mainly resulted from a-globin gene defects whichlocated in 16p13.3. a-thalassemia is classified as deletional or non-deletional accordingto the mutational.The most common mutation producing this syndrome is the Southeast Asian (- SEA ) double -globin gene deletion mechanism involved.

Technical Data
Mutation information	Variation site: N/A
	Zygosity: Heterozygous
	Allelic Frequency: 50%
Transcript	N/A
Chr position(GRCh37)	chr16:215396-234699 del
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℃
Expiry	36 months from the date of manufacture

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