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ASXL1 p.G646fs Reference Standard

CBP10641

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索取COA
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产品数据库
Introduction 
Format Genomic DNA
Description ASXL1 (ASXL Transcriptional Regulator 1) is a Protein Coding gene. Diseases associated with ASXL1 include Bohring-Opitz Syndrome and Myelodysplastic Syndrome. Among its related pathways are Metabolism of proteins and Deubiquitination.
   
Technical Data 
DNA Change: c.1934del
AA Change p.G646fs
Mutation type N/A
Zygosity Heterozygous
Allelic Frequency 50.00%
Transcript NM_015338.6
Cosmic ID N/A
Chr position(GRCh37) N/A
Buffer: Tris-EDTA
   
Product Information 
Intended Use Research Use Only
Unit Size 1ug
Concentration Download for COA
Purity Download for COA
DNA electrophoresis Download for COA
Sanger sequencing Download for COA
Storage 2-8℃
Expiry 36 months from the date of manufacture
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

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