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ARMC4 Recombinant monoclonal antibody, PBS Only

ARMC4 Uni-rAb® Recombinant Antibody for WB, Indirect ELISA
Cat No. 84004-3-PBS

产品说明书

CloneNo. 241122G4

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse

应用

WB, Indirect ELISA

RP11 691I13.1, Outer dynein arm-docking complex subunit 2, ODAD2, Armadillo repeat-containing protein 4, armadillo repeat containing 4

缓冲液配方:  PBS Only
PBS and Azide
PBS Only
偶联物:  Unconjugated
规格价格库存


产品信息

84004-3-PBS targets ARMC4 in WB, Indirect ELISA applications and shows reactivity with human, mouse samples.

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

CatNo: Ag22340

Product name: Recombinant human ARMC4 protein

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

Tag: GST

Domain: 690-1044 aa of BC140846

Sequence: QEHCAMAIYQCAEDKETRDLVRLHGGLKPLASLLNNTDNKERLAAVTGAIWKCSISKENVTKFREYKAIETLVGLLTDQPEEVLVNVVGALGECCQERENRVIVRKCGGIQPLVNLLVGINQALLVNVTKAVGACAVEPESMMIIDRLDGVRLLWSLLKNPHPDVKASAAWALCPCIKNAKDAGEMVRSFVGGLELIVNLLKSDNKEVLASVCAAITNIAKDQENLAVITDHGVVPLLSKLANTNNNKLRHHLAEAISRCCMWGRNRVAFGEHKAVAPLVRYLKSNDTNVHRATAQALYQLSEDADNCITMHENGAVKLLLDMVGSPDQDLQEAAAGCISNIRRLALATEKARYT

种属同源性预测
宿主/亚型 Rabbit / IgG
抗体类别 Recombinant
产品类型 Antibody
全称 armadillo repeat containing 4
别名 RP11 691I13.1, Outer dynein arm-docking complex subunit 2, ODAD2, Armadillo repeat-containing protein 4, armadillo repeat containing 4
计算分子量 1044 aa, 116 kDa
观测分子量116 kDa
GenBank蛋白编号BC140846
基因名称 ODAD2
Gene ID (NCBI) 55130
偶联类型 Unconjugated
形式Liquid
纯化方式Protein A purfication
UNIPROT IDQ5T2S8
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

ODAD2 contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects.

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