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GJB3 Polyclonal antibody

GJB3 Polyclonal Antibody for WB, IHC, IF-P, IP, ELISA
Cat No. 12880-1-AP

产品说明书

宿主/亚型

Rabbit / IgG

种属反应性

human, mouse, rat and More (1)

应用

WB, IHC, IF-P, IP, ELISA and More (1)

EKV, DFNA2B, DFNA2, CX31, Connexin-31

缓冲液配方:  PBS and Azide
PBS and Azide
偶联物:  Unconjugated
Unconjugated
规格: 

-/ -


经过测试的应用

Positive WB detected inmouse stomach tissue, mouse ovary tissue, HeLa cells
Positive IP detected inHeLa cells
Positive IHC detected inmouse placenta tissue, human ovary tumor tissue, human cervix tissue, human skin cancer tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0
Positive IF-P detected inhuman placenta tissue

推荐稀释比

应用推荐稀释比
Western Blot (WB)WB : 1:1000-1:4000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochemistry (IHC)IHC : 1:50-1:500
Immunofluorescence (IF)-PIF-P : 1:50-1:500
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

12880-1-AP targets GJB3 in WB, IHC, IF-P, IP, ELISA applications and shows reactivity with human, mouse, rat samples.

经测试应用 WB, IHC, IF-P, IP, ELISA Application Description
文献引用应用WB, IHC, IF
经测试反应性 human, mouse, rat
文献引用反应性human, mouse, rat, marmoset
免疫原 GJB3 fusion protein Ag3839 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 gap junction protein, beta 3, 31kDa
别名 EKV, DFNA2B, DFNA2, CX31, Connexin-31
计算分子量 270 aa, 31 kDa
观测分子量 31 kDa
GenBank蛋白编号BC012918
基因名称 GJB3
Gene ID (NCBI) 2707
RRIDAB_2110907
偶联类型 Unconjugated
形式 Liquid
纯化方式Antigen affinity purification
UNIPROT IDO75712
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

GJB3, also known as Connexin-31 (Cx31), belongs to the connexin family. Connexins are membrane-spanning proteins that assemble to form gap junction channels that facilitate the transfer of ions and small molecules between cells. Mutations in the gene of GJB3 have been described in patients with dominant and recessive hearing impairment and in patients with erythrokeratodermia variabilis (EKV).

实验方案

Product Specific Protocols
WB protocol for GJB3 antibody 12880-1-APDownload protocol
IHC protocol for GJB3 antibody 12880-1-APDownload protocol
IF protocol for GJB3 antibody 12880-1-APDownload protocol
IP protocol for GJB3 antibody 12880-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

发表文章

SpeciesApplicationTitle
humanWB

Cell Rep

Cochlear Cell Modeling Using Disease-Specific iPSCs Unveils a Degenerative Phenotype and Suggests Treatments for Congenital Progressive Hearing Loss.

Authors - Makoto Hosoya
mouseIHC

Stem Cells

FBXL12-Mediated Degradation of ALDH3 Is Essential for Trophoblast Differentiation during Placental Development.

Authors - Masaaki Nishiyama
mouseIF

J Neurosci

Glial-Specific Deletion of Med12 Results in Rapid Hearing Loss via Degradation of the Stria Vascularis.

Authors - Teng-Wei Huang
marmosetIF

Sci Rep

Distinct Expression Patterns Of Causative Genes Responsible For Hereditary Progressive Hearing Loss In Non-Human Primate Cochlea.

Authors - Makoto Hosoya
mouseIF

Placenta

In vitro fertilization causes excessive glycogen accumulation in mouse placenta.

Authors - Jie Dong
mouseIHC

J Pain Res

PMID: 29692624

Authors - Brice Bellessort
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