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顶部产品介绍抗原信息化学信息储存和溶解信息计算器

Anti-GPIHBP1 Polyclonal Antibody

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货号 TMAB-06670

Anti-GPIHBP1 Polyclonal Antibody 是一种 Rabbit 抗体，靶向 GPIHBP1。Anti-GPIHBP1 Polyclonal Antibody 可用于 IHC-P,IHC-Fr,IF。

Anti-GPIHBP1 Polyclonal Antibody

Anti-GPIHBP1 Polyclonal Antibody

一键复制产品信息
Rating icon 还可以
货号 TMAB-06670

Anti-GPIHBP1 Polyclonal Antibody 是一种 Rabbit 抗体，靶向 GPIHBP1。Anti-GPIHBP1 Polyclonal Antibody 可用于 IHC-P,IHC-Fr,IF。

规格价格库存数量
50 μL
¥ 1,160
5日内发货
100 μL
¥ 1,960
5日内发货
200 μL
¥ 2,795
5日内发货
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产品介绍

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产品描述
Anti-GPIHBP1 Polyclonal Antibody is a Rabbit antibody targeting GPIHBP1. Anti-GPIHBP1 Polyclonal Antibody can be used in IHC-P,IHC-Fr,IF.
Ig Type
IgG
反应种属
Human
应用IHC-PIHC-FrIF
推荐剂量
IHC-P: 1:100-500; IHC-Fr: 1:100-500; IF: 1:100-500
抗体种类
Polyclonal
宿主来源Rabbit
亚细胞定位Cell membrane. Localized at the cell surface.
构建方式Polyclonal Antibody
纯化方式Protein A purified
性状Liquid
缓冲液0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
浓度1mg/ml
研究背景GPIHBP1 (glycosylphosphatidylinositol anchored high density lipoprotein binding protein 1) is a capillary endothelial cell protein that provides a platform for LPL-mediated processing of chylomicrons. Consisting of 184 amino acids, GPIHBP1 is a single-pass membrane protein that may be regulated by dietary factors and by PPARγ. Mutations in the gene encoding GPIHBP1 are linked to chylomicronemia syndrome, a rare genetic disorder caused by LPL deficiency and is characterized by enlarged liver and spleen, inflammation of the pancreas, fatty deposits under the skin and possibly deposits in the retina of the eye.
抗原信息
免疫原
KLH conjugated synthetic peptide: human GPIHBP1
抗原种属
Human
基因名称
GPIHBP1
基因ID
338328
蛋白名称
Glycosylphosphatidylinositol-anchored high density lipoprotein-binding protein 1
Uniprot ID
Q8IV16
功能
Plays a key role in the lipolytic processing of chylomicrons.
化学信息
分子量Theoretical: 18 kDa.
储存&溶解度
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.
运输方式Shipping with blue ice.

计算器

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