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基因檢測(cè)標(biāo)準(zhǔn)品 > 遺傳性耳聾 > CBPD0017SMN1 E7-E8Del (muscle atrophy) Reference Standard

SMN1 E7-E8Del (muscle atrophy) Reference Standard
名稱 SMN1 E7-E8Del (muscle atrophy) Reference Standard
型號(hào) CBPD0017
報(bào)價(jià)
特點(diǎn) SMN1 E7-E8Del (muscle atrophy) Reference Standard
  • 詳細(xì)內(nèi)容

SMN1 E7-E8Del (muscle atrophy) Reference Standard

Introduction
FormatGenomic DNA
DescriptionSpinal 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 numberSMN1  CN=0
SMN2  CN=2
DefinitionSMN1  Loss 
SMN2  Normal
　　
MLPA Result Graph　

SMN1 E7-E8Del (muscle atrophy) Reference Standard

 
Product Information　
Intended UseResearch Use Only
Unit Size1ug
ConcentrationDownload for COA
PuroficationDownload for COA
DNA electrophoresisDownload for COA
Sanger sequencingDownload for COA
Storage2-8°C
Expiry36 months from the date of manufacture


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