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當(dāng)前位置:首頁(yè)資料下載Utrophin抗原,肌營(yíng)養(yǎng)不良蛋白相關(guān)蛋白1抗原

Utrophin抗原,肌營(yíng)養(yǎng)不良蛋白相關(guān)蛋白1抗原

發(fā)布時(shí)間:2024/12/18點(diǎn)擊次數(shù):227

Recombinant human Utrophin   

DHTX; Disrupted in heterotaxy; p63; UV radiation resistance associated; UV radiation resistance associated gene; UV radiation resistance associated gene protein; UV radiation resistance-associated gene protein; UtrophinUtrophin_HUMAN.    

濃度:1mg/ ml

來(lái)源:Recombinant Human

純度:≥95% SDS-PAGE

表達(dá)系統(tǒng):Wheat germ

標(biāo)簽:GST tag N-Terminus

蛋白長(zhǎng)度:Protein fragment

內(nèi)毒素水平:<1.000 Eu/µg

純化方法:HPLC

應(yīng)用:SDS-PAGE,Western blot,ELISA

Biological activity,immunology research

保存:-20℃

保質(zhì)期:1年

Dystrophin and utrophin are related structural, Actin-binding proteins that are involved in anchoring the cytoskeleton to the plasma membrane. Dystrophin is the protein product of the Duchenne/Becker muscular dystrophy gene. Dystrophin expression is found in muscle and brain tissues, where it is localized to the inner surface of the plasma membrane. It has been speculated that alternative splicing of the carboxy terminus allows dystrophin to interact with a variety of proteins. Research has shown that the loss of dystrophin-associated proteins in Duchenne afflicted muscle is due to the absence of dystrophin rather than to muscle degradation and that the lack of dystrophin results in the loss of linkage between the cytoskeleton and the extracellular matrix. Evidence suggests that the upregulation of utrophin can reduce the dystrophic pathology.


抗體

產(chǎn)品名稱:Rabbit Anti-Utrophin antibody

Rabbit Anti-Utrophin  

別名:DMDL; DRP 1; DRP; DRP-1; DRP1; Dystrophin like protein; Dystrophin related protein 1; Dystrophin related protein; Dystrophin-related protein 1; FLJ23678; UTRN; UTRO_HUMAN; Utrophin (homologous to dystrophin); Utrophin     

來(lái)源:Rabbit

克隆類型:Polyclonal

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反應(yīng):Human (predicted: Mouse,Rat,Pig,Sheep,Cow,Chicken,Dog)

理論分子量:394kDa

免疫原:KLH conjugated synthetic peptide derived from Human Utrophin 

保存:-20
保質(zhì)期:1

 

單克隆抗體

產(chǎn)品名稱:Anti-Utrophin antibody

Mouse Anti-Utrophin 

別名:DMDL; DRP 1; DRP; DRP-1; DRP1; Dystrophin like protein; Dystrophin related protein 1; Dystrophin related protein; Dystrophin-related protein 1; FLJ23678; UTRN; UTRO_HUMAN; Utrophin (homologous to dystrophin); Utrophin  

來(lái)源:Mouse

克隆類型:Monoclonal

濃度:1mg/ml

亞型:IgG

應(yīng)用: WB=1:1000-1:2000,Elisa=1:1000-1:2000,IHC-P=1:100-500,IHC-F=1:100-500,ICC/IF=1:100-500,IF=1:100-500

反應(yīng): Human 

理論分子量:394kDa

免疫原:KLH conjugated synthetic peptide derived from Human Utrophin  

保存:-20
保質(zhì)期:1

Dystrophin and utrophin are related structural, Actin-binding proteins that are involved in anchoring the cytoskeleton to the plasma membrane. Dystrophin is the protein product of the Duchenne/Becker muscular dystrophy gene. Dystrophin expression is found in muscle and brain tissues, where it is localized to the inner surface of the plasma membrane. It has been speculated that alternative splicing of the carboxy terminus allows dystrophin to interact with a variety of proteins. Research has shown that the loss of dystrophin-associated proteins in Duchenne afflicted muscle is due to the absence of dystrophin rather than to muscle degradation and that the lack of dystrophin results in the loss of linkage between the cytoskeleton and the extracellular matrix. Evidence suggests that the upregulation of utrophin can reduce the dystrophic pathology.

 

 


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