Gjb4 Antibodies

AND Gjb4 ELISA kits, Gjb4 Proteins

Many biological assays use antibodies to detect Gjb4, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with Gjb4 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop Gjb4 antibodies...

We validate the specificity of these antibodies to Gjb4 by testing them on tissues known to express Gjb4 positively and negatively. Browse below to find the Gjb4 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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Gjb4 Infographic by Boster Bio

All Gjb4 Products

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Specificity

Applications

Price

GJB4 (NM_153212) Human Recombinant Protein

$813
Cat # PROTQ9NTQ9
20 µg

GJB4 (NM_153212) Human Over-expression Lysate

Human

$628
Cat # LS127534
100 µg

Gjb4 Overview

Facts about Gap junction beta-4 protein.

Gap junction beta-4 protein (Gjb4)

One gap junction consists of a cluster of closely packed pairs of transmembrane channels, the connexons, through which materials of low MW diffuse from one cell to a neighboring cell. .

Gene Information

Mouse
Gene Name:	Gjb4
Uniprot:	Q02738
Entrez:	14621

Family

Belongs to:

connexin family

Alternative Names

beta 4; Connexin 30.3; connexin-30.3; CX30.3; EKV; gap junction beta-4 protein; gap junction protein, beta 4 (connexin 30.3); gap junction protein, beta 4, 30.3kDa; GJB4; MGC21116

Molecular Weight

Mass (kDA):
30.389 kDA

Genomic Context


Mouse

Location:	4 D2.2\|4 61.51 cM
Sequence:	4;

Tissue Specificity

Expressed in skin.

Diseases

Erythrokeratodermia Variabilis
Skin Diseases, Genetic
Hyperkeratosis
Erythema
Sensorineural Hearing Loss (disorder)
Dermatologic Disorders
Keratosis
Bullous Congenital Ichthyosiform Erythroderma (disorder)
Complete Hearing Loss
Palmoplantar Keratosis

Hidrotic Ectodermal Dysplasia
Dystrophia Unguium
Ainhum
Dysplasia
Nails, Malformed

Pathways

Cornification
Keratinization
Dna Amplification
Keratinocyte Differentiation
Pathogenesis
Localization

PTMs

Disulfide bond

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/Gjb4

References

PMID: 1512260 by Hennemann H., et al. Two gap junction genes, connexin 31.1 and 30.3, are closely linked on mouse chromosome 4 and preferentially expressed in skin.

PMID: 15692151 by Sun J., et al. Cochlear gap junctions coassembled from Cx26 and 30 show faster intercellular Ca2+ signaling than homomeric counterparts.