Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
预测分子量
55 kDa
纯化方式
Affinity Purification
标记类型
Un-conjugated
克隆性
Monoclonal
来源
Rabbit
免疫源
Recombinant protein of human DFNA5/GSDME
实际分子量
55 kDa
反应种属
HumanMouseRat
产品别名
DFNA5; ICERE-1
货号: RMA01503
DFNA5/GSDME Recombinant Rabbit mAb
应用:
FCIPWB
反应种属:
HumanMouseRat
¥ 1280
/ 50ul
库存充足
50ul100ul
产品详情
产品特性
应用
FCIPWB
Uniprot
O60443
GeneID
1687
Isotype
IgG
Background
Hearing impairment is a heterogeneous condition with over 40 loci described. The protein encoded by this gene is expressed in fetal cochlea, however, its function is not known. Nonsyndromic hearing impairment is associated with a mutation in this gene. Three transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]