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Anti-VLDLR Antibody (3U184)

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产品编号 TMAY-01596

Anti-VLDLR Antibody (3U184) 是一种 Mouse 抗体,靶向 VLDLR。Anti-VLDLR Antibody (3U184) 可用于 ELISA。

Anti-VLDLR Antibody (3U184)

Anti-VLDLR Antibody (3U184)

Rating icon 还可以
产品编号 TMAY-01596

Anti-VLDLR Antibody (3U184) 是一种 Mouse 抗体,靶向 VLDLR。Anti-VLDLR Antibody (3U184) 可用于 ELISA。

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产品介绍

生物活性
产品描述
Anti-VLDLR Antibody (3U184) is a Mouse antibody targeting VLDLR. Anti-VLDLR Antibody (3U184) can be used in ELISA.
Ig Type
Monoclonal Mouse IgG1
克隆号
3U184
交叉反应
Human
应用
ELISA
推荐剂量
ELISA: 1:1000-1:2000
抗体种类
Monoclonal
宿主来源Mouse
构建方式This antibody was produced from a hybridoma resulting from the fusion of a mouse myeloma with B cells obtained from a mouse immunized with purified, recombinant Human VLDLR / VLDL Receptor (rh VLDLR / VLDL Receptor; TMPY-01085; NP_003374.3; Met 1-Ser 797). The IgG fraction of the cell culture supernatant was purified by Protein A affinity chromatography.
纯化方式Protein A
性状Liquid
缓冲液0.2 μm filtered solution in PBS
研究背景The very low density lipoprotein receptor, known as VLDLR, is a single-pass type 1 integral membrance protein and a member of the LDL receptor family. This receptor family includes LDL receptor, LRP, megalin, VLDLR and ApoER2, and is characterized by a cluster of cysteine-rich class A repeats, epidermal growth factor (EGF)-like repeats, YWTD repeats and an O-linked sugar sdomain. VLDLR contains 3 EGF-like domains, 8 LDL-receptor class A domains, as well as 6 LDL-receptor class B repeats, and is abundant in heart, skeletal muscle, also ovary and kidney, but not in liver. VLDLR 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. VLDLR mediates the phosphorylation of mDab1 (mammalian disabled protein) via binding to Reelin, and induces the modulation of Tau phosphorylation. This pathway regulates the migration of neurons along with the radial glial fiber network during brain development. Defects of VLDLR may be the cause of VLDLR-associated cerebellar hypoplasia (VLDLRCH), a syndrome characterized by moderate-to-profound mental retardation, delayed ambulation, and predominantly truncal ataxia.
偶联与修饰
偶联
Unconjugated
抗原信息
免疫原
Recombinant Human VLDLR / VLDL Receptor protein (TMPY-01085)
抗原种属
Human
存储&运输
储存方式Store at 2°C-8°C for 1 month. Store at -20°C or -80°C for 12 months. Avoid repeated freeze-thaw cycles. Preservative-Free.
运输方式Shipping with blue ice.

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