DFNA5/GSDME Rabbit mAb

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商品货号： PRM8258

适应性： 人,小鼠,大鼠

￥800元

规格：

50ul

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说明书

商品描述

发货日期：现货
靶点-Target： DFNA5
反应性-Reactivity：人,小鼠,大鼠
应用-Applications： WB,IF,IP,ELISA
MW(Calculated)： 55kD
MW(Observed)： 55kD
宿主物种-Host Species： Rabbit
同种型-Isotype： IgG,Kappa
偶联-Conjugate： Unmodified
推荐稀释比： WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
组成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
纯化工艺： Protein A
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0634R
特异性： Endogenous
基因名称： DFNA5
蛋白名称： Non-syndromic hearing impairment protein 5
别名： DFNA5;ICERE1;Non-syndromic hearing impairment protein 5;Inversely correlated with estrogen receptor expression 1;ICERE-1
Organism-1： Human
基因ID-1： 1687
SwissProt-1： O60443
Organism-2： Mouse
SwissProt-2： Q9Z2D3
背景： 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],
细胞定位： Membrane, Cytoplasm

DFNA5/GSDME Rabbit mAb

Catalog No PRM8258

Product information

发货日期：现货
靶点-Target： DFNA5
反应性-Reactivity：人,小鼠,大鼠
应用-Applications： WB,IF,IP,ELISA
MW(Calculated)： 55kD
MW(Observed)： 55kD
宿主物种-Host Species： Rabbit
同种型-Isotype： IgG,Kappa
偶联-Conjugate： Unmodified
推荐稀释比： WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
组成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
纯化工艺： Protein A
储存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆号： PT0634R
特异性： Endogenous
基因名称： DFNA5
蛋白名称： Non-syndromic hearing impairment protein 5
别名： DFNA5;ICERE1;Non-syndromic hearing impairment protein 5;Inversely correlated with estrogen receptor expression 1;ICERE-1
Organism-1： Human
基因ID-1： 1687
SwissProt-1： O60443
Organism-2： Mouse
SwissProt-2： Q9Z2D3
背景： 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],
细胞定位： Membrane, Cytoplasm

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