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南京科佰生物科技有限公司

中級(jí)會(huì)員 | 第11年

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產(chǎn)品簡介

SMN1 E7-E8Del (muscle atrophy) Reference Standard

SMN1 E7-E8Del (muscle atrophy) Reference Standard

Introduction
Format	Genomic DNA
Description	Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disease characterized by progressive muscle weakness and atrophy caused by the degeneration of motor neurons in the anterior horn of the spinal cord. The disease is the number one fatal genetic disease in infancy, and it is estimated that there is one case in every 10,000 live births; the carrier rate of the general population is about 1/50, and the carrier rate of the domestic population is about 1/42.

Technical Data
Copy number	SMN1 CN=0
Copy number	SMN2 CN=2
Definition	SMN1 Loss
Definition	SMN2 Normal

MLPA Result Graph


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	Download for COA
Storage	2-8°C
Expiry	36 months from the date of manufacture