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MTCO2 rabbit Rabbit mAb

商品貨號： PRM8612

適應(yīng) 性： 人,

￥800元

規(guī)格：

50ul

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商品描述

發(fā)貨日期：現(xiàn)貨
靶點-Target： COX2
反應(yīng)性-Reactivity：人,
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 26kD
MW(Observed)： 21kD
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
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0385R
特異性： Endogenous
基因名稱： MT-CO2 COII COXII MTCO2
蛋白名稱： Cytochrome c oxidase subunit 2 (Cytochrome c oxidase polypeptide II)
Organism-1： Human
基因ID-1： 4513
SwissProt-1： P00403
Organism-2： Mouse
SwissProt-2： P00405
Organism-3： Rat
SwissProt-3： P00406
背景： cofactor:Copper A.,disease:Defects in MT-CO2 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]; also called mitochondrial complex IV deficiency. COX deficiency is a clinically heterogeneous disorder. The clinical features are ranging from isolated myopathy to severe multisystem disease, with onset from infancy to adulthood.,disease:Defects in MT-CO2 are associated with tumor formation.,function:Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1.,similarity:Belongs to the cytochrome c oxidase subunit 2 family.,
細(xì)胞定位： Cytoplasmic

MTCO2 rabbit Rabbit mAb

Catalog No PRM8612

Product information

發(fā)貨日期：現(xiàn)貨
靶點-Target： COX2
反應(yīng)性-Reactivity：人,
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 26kD
MW(Observed)： 21kD
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
儲存： -15°C to -25°C/1 year(Do not lower than -25°C)
克隆性： Monoclonal
克隆號： PT0385R
特異性： Endogenous
基因名稱： MT-CO2 COII COXII MTCO2
蛋白名稱： Cytochrome c oxidase subunit 2 (Cytochrome c oxidase polypeptide II)
Organism-1： Human
基因ID-1： 4513
SwissProt-1： P00403
Organism-2： Mouse
SwissProt-2： P00405
Organism-3： Rat
SwissProt-3： P00406
背景： cofactor:Copper A.,disease:Defects in MT-CO2 are a cause of cytochrome c oxidase deficiency (COX deficiency) [MIM:220110]; also called mitochondrial complex IV deficiency. COX deficiency is a clinically heterogeneous disorder. The clinical features are ranging from isolated myopathy to severe multisystem disease, with onset from infancy to adulthood.,disease:Defects in MT-CO2 are associated with tumor formation.,function:Cytochrome c oxidase is the component of the respiratory chain that catalyzes the reduction of oxygen to water. Subunits 1-3 form the functional core of the enzyme complex. Subunit 2 transfers the electrons from cytochrome c via its binuclear copper A center to the bimetallic center of the catalytic subunit 1.,similarity:Belongs to the cytochrome c oxidase subunit 2 family.,
細(xì)胞定位： Cytoplasmic

Hunan UPT Biotechnology Co.,Ltd

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E-mail：service@uptbio.com

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