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BBIP1 Polyclonal antibody

BBIP1 Polyclonal Antibody for WB, ELISA
Cat No. 33050-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human

应用

WB, ELISA

BBIP10, BBSome Interacting Protein 1, BBSome-interacting protein 1, BBSome-interacting protein of 10 kDa, NCRNA00081

缓冲液配方:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
偶联物:  Unconjugated
Unconjugated
规格价格库存


经过测试的应用

Positive WB detected inA549 cells, PANC-1 cells, U-87 MG cells

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:500-1:3000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

产品信息

33050-1-AP targets BBIP1 in WB, ELISA applications and shows reactivity with human samples.

经测试应用 WB, ELISA Application Description
经测试反应性 human
免疫原

CatNo: Ag36924

Product name: Recombinant human BBIP1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-92 aa of BC015550

Sequence: MLKAAAKRPELSGKNTISNNSDMAEVKSMFREVLPKQGPLFVEDIMTMVLCKPKLLPLKSLTLEKLEKMHQAAQNTIRQQEMAEKDQRQITH*

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Polyclonal
产品类型 Antibody
全称 non-protein coding RNA 81
别名 BBIP10, BBSome Interacting Protein 1, BBSome-interacting protein 1, BBSome-interacting protein of 10 kDa, NCRNA00081
观测分子量22 kDa
GenBank蛋白编号BC015550
基因名称 NCRNA00081
Gene ID (NCBI) 92482
RRIDAB_3742837
偶联类型 Unconjugated
形式Liquid
纯化方式Antigen affinity Purification
UNIPROT IDA8MTZ0
储存缓冲液 PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
储存条件Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

背景介绍

The BBIP1 protein is a key component of the BBSome complex and was identified due to its role in the pathogenesis of Bardet-Biedl syndrome (BBS). This protein localizes to the base of cellular cilia and plays an indispensable role in ciliary assembly, maintenance, and signal transduction. As an adapter for membrane protein trafficking, BBIP1 works in coordination with other members of the BBSome to precisely transport specific cargo proteins into the cilium, an important cellular organelle. Loss of its function disrupts the stability of the BBSome complex, leading to abnormalities in ciliary structure and function. This, in turn, causes various clinical symptoms of BBS, including retinal degeneration, obesity, and polydactyly. Therefore, research on BBIP1 is central to understanding the molecular basis of cilia-related diseases (ciliopathies).

实验方案

Product Specific Protocols
WB protocol for BBIP1 antibody 33050-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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