GJB6 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-12383
Catalog Number: E-AB-12383
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB,IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: WB,IHC,ELISA
Datasheet, Questions? Contact us!
Background:
Gap junctions allow the transport of ions and metabolites between the cytoplasm of adjacent cells. They are formed by two hemichannels, made up of six connexin proteins assembled in groups. Each connexin protein has four transmembrane segments, two extracellular loops, a cytoplasmic loop formed between the two inner transmembrane segments, and the N- and C-terminus both being in the cytoplasm. The specificity of the gap junction is determined by which connexin proteins comprise the hemichannel. In the past, connexin protein names were based on their molecular weight, however the new nomenclature uses sequential numbers based on which form (alpha or beta) of the gap junction is present. This gene encodes one of the connexin proteins. Mutations in this gene have been found in some forms of deafness and in some families with hidrotic ectodermal dysplasia.
Research Area: Neuroscience, Signal Transduction
Synonyms:
Connexin 30, Connexin-30, Cx30, CXB6, DFNA3, DFNA3B, DFNB1B, ECTD2, ectodermal dysplasia 2, hidrotic (Clouston syndrome), ED2, EDH, Gap junction beta 6 protein, Gap junction beta-6 protein, gap junction protein, beta 6 (connexin 30), gap junction protein, beta 6, Gap junction protein, beta 6, 30kDa, GJB6, HED, HED2, NSRD1
Immunogen: Synthetic peptide of human GJB6
Swissprot: O95452
Gene Accession: NP_006774
Calculated MW: 30 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.3 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:25-1:100
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-84801/sc-84802
Gap junctions allow the transport of ions and metabolites between the cytoplasm of adjacent cells. They are formed by two hemichannels, made up of six connexin proteins assembled in groups. Each connexin protein has four transmembrane segments, two extracellular loops, a cytoplasmic loop formed between the two inner transmembrane segments, and the N- and C-terminus both being in the cytoplasm. The specificity of the gap junction is determined by which connexin proteins comprise the hemichannel. In the past, connexin protein names were based on their molecular weight, however the new nomenclature uses sequential numbers based on which form (alpha or beta) of the gap junction is present. This gene encodes one of the connexin proteins. Mutations in this gene have been found in some forms of deafness and in some families with hidrotic ectodermal dysplasia.
Research Area: Neuroscience, Signal Transduction
Synonyms:
Connexin 30, Connexin-30, Cx30, CXB6, DFNA3, DFNA3B, DFNB1B, ECTD2, ectodermal dysplasia 2, hidrotic (Clouston syndrome), ED2, EDH, Gap junction beta 6 protein, Gap junction beta-6 protein, gap junction protein, beta 6 (connexin 30), gap junction protein, beta 6, Gap junction protein, beta 6, 30kDa, GJB6, HED, HED2, NSRD1
Immunogen: Synthetic peptide of human GJB6
Swissprot: O95452
Gene Accession: NP_006774
Calculated MW: 30 kDa
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.3 mg/mL
Dilution: WB 1:500-1:2000, IHC 1:25-1:100
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-84801/sc-84802
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