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SDHA Rabbit mAb

商品貨號(hào)： PRM8616

適應(yīng) 性： 人,小鼠,大鼠

￥800元

規(guī)格：

50ul

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MSDS

說(shuō)明書

商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： SDHA
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 73kD
MW(Observed)： 73kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1000;WB 1:1000-5000;IF 1:200-1000;ELISA 1:5000-20000;IP 1:50-200
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)： PT0711R
特異性： Endogenous
基因名稱： SDHA
蛋白名稱： Succinate dehydrogenase [ubiquinone] flavoprotein subunit mitochondrial
別名： SDHA;SDH2;SDHF;Succinate dehydrogenase [ubiquinone] flavoprotein subunit;mitochondrial;Flavoprotein subunit of complex II;Fp
Organism-1： Human
基因ID-1： 6389
SwissProt-1： P31040
Organism-2： Mouse
基因ID-2： 66945
SwissProt-2： Q8K2B3
Organism-3： Rat
基因ID-3： 157074
SwissProt-3： Q920L2
背景： This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014],
細(xì)胞定位： Cytoplasmic

SDHA Rabbit mAb

Catalog No PRM8616

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： SDHA
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 73kD
MW(Observed)： 73kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1000;WB 1:1000-5000;IF 1:200-1000;ELISA 1:5000-20000;IP 1:50-200
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)： PT0711R
特異性： Endogenous
基因名稱： SDHA
蛋白名稱： Succinate dehydrogenase [ubiquinone] flavoprotein subunit mitochondrial
別名： SDHA;SDH2;SDHF;Succinate dehydrogenase [ubiquinone] flavoprotein subunit;mitochondrial;Flavoprotein subunit of complex II;Fp
Organism-1： Human
基因ID-1： 6389
SwissProt-1： P31040
Organism-2： Mouse
基因ID-2： 66945
SwissProt-2： Q8K2B3
Organism-3： Rat
基因ID-3： 157074
SwissProt-3： Q920L2
背景： This gene encodes a major catalytic subunit of succinate-ubiquinone oxidoreductase, a complex of the mitochondrial respiratory chain. The complex is composed of four nuclear-encoded subunits and is localized in the mitochondrial inner membrane. Mutations in this gene have been associated with a form of mitochondrial respiratory chain deficiency known as Leigh Syndrome. A pseudogene has been identified on chromosome 3q29. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jun 2014],
細(xì)胞定位： Cytoplasmic

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