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DFNA5/GSDME Rabbit mAb

商品貨號(hào)： PRM8258

適應(yīng) 性： 人,小鼠,大鼠

￥800元

規(guī)格：

50ul

說(shuō)明書(shū)

商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： DFNA5
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IF,IP,ELISA
MW(Calculated)： 55kD
MW(Observed)： 55kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0634R
特異性： Endogenous
基因名稱(chēng)： DFNA5
蛋白名稱(chēng)： Non-syndromic hearing impairment protein 5
別名： 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],
細(xì)胞定位： Membrane, Cytoplasm

DFNA5/GSDME Rabbit mAb

Catalog No PRM8258

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： DFNA5
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IF,IP,ELISA
MW(Calculated)： 55kD
MW(Observed)： 55kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： WB 1:2000-1:10000;IF 1:200-1:1000;ELISA 1:5000-1:20000;IP 1:50-1:200;
組成： PBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
純化工藝： Protein A
儲(chǔ)存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號(hào)： PT0634R
特異性： Endogenous
基因名稱(chēng)： DFNA5
蛋白名稱(chēng)： Non-syndromic hearing impairment protein 5
別名： 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],
細(xì)胞定位： Membrane, Cytoplasm

Hunan UPT Biotechnology Co.,Ltd

Website：www.tjdqdt.com Servive hotline :4006916686

E-mail：service@uptbio.com

Address：

Room 402, Building 13, Xinggong International Industrial Park, 100 Guyuan Road, Yuelu District, Changsha City, Hunan Province, China.

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