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上海允麥生物科技有限公司
中級會員·7年
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- 麥經(jīng)理
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Recombinant human VLDL Receptor
Very low density lipoprotein receptor; VLDL R; VLDLR; VLDL-R; VLDLRCH.
濃度：1mg/ ml
來源：Recombinant Human
純度：≥95% SDS-PAGE
表達系統(tǒng)：HEK 293 cells
標簽：His tag C-Terminus
蛋白長度：Full length protein
內(nèi)毒素水平：<1.000 Eu/µg
純化方法：HPLC
應用：SDS-PAGE，Western blot，ELISA
Biological activity,immunology research
保存：-20℃
保質(zhì)期：1年
VLDL (very low density lipoprotein) cholesterol is one of the three major types of cholesterol found in blood. VLDL receptor plays an essential role in triglyceride metabolism. It binds VLDL and transports it into cells by endocytosis. In order to be internalized, the receptor-ligand complexes must first cluster into clathrin coated pits. Binding to Reelin induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation.
產(chǎn)品名稱：Rabbit Anti-VLDL Receptor antibody
Rabbit Anti-VLDL Receptor
別名：Very low density lipoprotein receptor; VLDL R; VLDLR; VLDL-R; VLDLRCH.
來源：Rabbit
克隆類型：Polyclonal
濃度：1mg/ml
亞型：IgG
應用： 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: Human (predicted: Mouse,Rat,Rabbit,Pig,Dog,Horse)
理論分子量：93kDa
免疫原：KLH conjugated synthetic peptide derived from human VLDL Receptor
保存：-20℃
保質(zhì)期：1年
單克隆抗體
產(chǎn)品名稱：Anti-VLDL Receptor antibody
Mouse Anti-VLDL Receptor
別名：Very low density lipoprotein receptor; VLDL R; VLDLR; VLDL-R; VLDLRCH.
來源：Mouse
克隆類型：Monoclonal
濃度：1mg/ml
亞型：IgG
應用： 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: Human
理論分子量：93kDa
免疫原：KLH conjugated synthetic peptide derived from human VLDL Receptor
保存：-20℃
保質(zhì)期：1年
VLDL (very low density lipoprotein) cholesterol is one of the three major types of cholesterol found in blood. VLDL receptor plays an essential role in triglyceride metabolism. It binds VLDL and transports it into cells by endocytosis. In order to be internalized, the receptor-ligand complexes must first cluster into clathrin coated pits. Binding to Reelin induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation.
