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验证数据展示

  • WB analysis using 29778-1-AP (same clone as 29778-1-PBS)

    WB analysis using 29778-1-AP (same clone as 29778-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 29778-1-AP (RPGRIP1L antibody) at dilution of 1:1000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 29778-1-PBS in a different storage buffer formulation.

  • WB analysis using 29778-1-AP (same clone as 29778-1-PBS)

    WB analysis using 29778-1-AP (same clone as 29778-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 29778-1-AP (RPGRIP1L antibody) at dilution of 1:2500 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 29778-1-PBS in a different storage buffer formulation.

RPGRIP1L Polyclonal antibody, PBS Only

RPGRIP1L Polyclonal Antibody for WB, Indirect ELISA
Cat No. 29778-1-PBS

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat

应用

WB, Indirect ELISA

别名

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

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产品信息

29778-1-PBS targets RPGRIP1L in WB, Indirect ELISA applications and shows reactivity with human, mouse, rat samples.

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

CatNo: Ag31168

Product name: Recombinant human RPGRIP1L protein

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

Tag: GST

Domain: 1-140 aa of NM_015272

Sequence: MSGPTDETAGDLPVKDTGLNLFGMGGLQETSTTRTMKSRQAVSRVSREELEDRFLRLHDENILLKQHARKQEDKIKRMATKLIRLVNDKKRYERVGGGPKRLGRDVEMEEMIEQLQEKVHELEKQNETLKNRLISAKQQL

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 RPGRIP1-like
别名
计算分子量 151 kDa
观测分子量151 kDa
GenBank蛋白编号NM_015272
基因名称 RPGRIP1L
Gene ID (NCBI) 23322
RRIDAB_2923607
偶联类型 Unconjugated
形式Liquid
纯化方式Antigen affinity purification
UNIPROT IDQ68CZ1
储存缓冲液 PBS only, pH 7.3.
储存条件Store at -80°C.
The product is shipped with ice packs. Upon receipt, store it immediately at -80°C

背景介绍

RPGRIP1L, also named as FTM, KIAA1005, belongs to the RPGRIP1 family. It negatively regulates signaling through the G-protein coupled thromboxane A2 receptor. RPGRIP1L may be involved in mechanisms like programmed cell death, craniofacial development, patterning of the limbs, and formation of the left-right axis.(PMID:17558409) Defects in RPGRIP1L are the cause of Joubert syndrome type 7 (JBTS7). Defects in RPGRIP1L are the cause of Meckel syndrome type 5 (MKS5).

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