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Mitofusin-2 Rabbit mAb

商品貨號(hào)： PRM8283

適應(yīng) 性： 人,小鼠,大鼠

￥7000元

規(guī)格：

500ul

在線咨詢

MSDS

說(shuō)明書

商品描述

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Mfn2
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 86kD
MW(Observed)： 86kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1:1000;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)： PT0529R
特異性： Endogenous
基因名稱： MFN2
蛋白名稱： Mitofusin-2
別名： MFN2;CPRP1;KIAA0214;Mitofusin-2;Transmembrane GTPase MFN2
Organism-1： Human
基因ID-1： 9927
SwissProt-1： O95140
Organism-2： Mouse
基因ID-2： 170731
SwissProt-2： Q80U63
Organism-3： Rat
SwissProt-3： Q8R500
背景： This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008],
細(xì)胞定位： Mitochondrion outer membrane

Mitofusin-2 Rabbit mAb

Catalog No PRM8283

Product information

發(fā)貨日期：現(xiàn)貨
靶點(diǎn)-Target： Mfn2
反應(yīng)性-Reactivity：人,小鼠,大鼠
應(yīng)用-Applications： WB,IHC,IF,IP,ELISA
MW(Calculated)： 86kD
MW(Observed)： 86kD
宿主物種-Host Species： Rabbit
同種型-Isotype： IgG,Kappa
偶聯(lián)-Conjugate： Unmodified
推薦稀釋比： IHC 1:200-1:1000;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)： PT0529R
特異性： Endogenous
基因名稱： MFN2
蛋白名稱： Mitofusin-2
別名： MFN2;CPRP1;KIAA0214;Mitofusin-2;Transmembrane GTPase MFN2
Organism-1： Human
基因ID-1： 9927
SwissProt-1： O95140
Organism-2： Mouse
基因ID-2： 170731
SwissProt-2： Q80U63
Organism-3： Rat
SwissProt-3： Q8R500
背景： This gene encodes a mitochondrial membrane protein that participates in mitochondrial fusion and contributes to the maintenance and operation of the mitochondrial network. This protein is involved in the regulation of vascular smooth muscle cell proliferation, and it may play a role in the pathophysiology of obesity. Mutations in this gene cause Charcot-Marie-Tooth disease type 2A2, and hereditary motor and sensory neuropathy VI, which are both disorders of the peripheral nervous system. Defects in this gene have also been associated with early-onset stroke. Two transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008],
細(xì)胞定位： Mitochondrion outer membrane

Hunan UPT Biotechnology Co.,Ltd

Website：m.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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