Product Name
GJB6, Blocking Peptide
Product Synonym Names
Gap junction beta-6 protein; Connexin-30; Cx30; GJB6
Product Gene Name
GJB6 blocking peptide
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Antibody/Peptide Pairs
GJB6 peptide (MBS9221332) is used for blocking the activity of GJB6 antibody (MBS9212066)
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
3D Structure
ModBase 3D Structure for O95452
Specificity
The synthetic peptide sequence used to generate the antibody was selected from the N-term region of human GJB6. A 10 to 100 fold molar excess to antibody is recommended. Precise conditions should be optimized for a particular assay.
Form/Format
The synthetic peptide was lyophilized with 100% acetonitrile and is supplied as a powder. Reconstitute with 0.1 ml deionized water for a final concentration of 1 mg/ml.
Cellular Location
Cell membrane; Multi-pass membrane protein. Cell junction, gap junction
Preparation and Storage
Maintain refrigerated at 2-8 degree C for up to 6 months. For long term storage store at -20 degree C.
Other Notes
Small volumes of GJB6 blocking peptide vial(s) may occasionally become entrapped in the seal of the product vial during shipment and storage. If necessary, briefly centrifuge the vial on a tabletop centrifuge to dislodge any liquid in the container`s cap. Certain products may require to ship with dry ice and additional dry ice fee may apply.
Related Product Information for
GJB6 blocking peptide
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.
NCBI/Uniprot data below describe general gene information for GJB6. It may not necessarily be applicable to this product.
NCBI Accession #
O95452.2
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UniProt Primary Accession #
O95452
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UniProt Secondary Accession #
Q5Q1H9; Q5Q1I0; Q5Q1I1; Q5T5U0; Q8IUP0; B3KQN2[Other Products]
UniProt Related Accession #
O95452[Other Products]
Molecular Weight
30,387 Da
NCBI Official Full Name
Gap junction beta-6 protein
NCBI Official Synonym Full Names
gap junction protein beta 6
NCBI Official Symbol
GJB6 [Similar Products]
NCBI Official Synonym Symbols
ED2; EDH; HED; CX30; HED2; DFNA3; ECTD2; DFNA3B; DFNB1B
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NCBI Protein Information
gap junction beta-6 protein
UniProt Protein Name
Gap junction beta-6 protein
UniProt Synonym Protein Names
Connexin-30; Cx30
Protein Family
Gap junction beta-6 protein
UniProt Gene Name
GJB6 [Similar Products]
UniProt Synonym Gene Names
Cx30 [Similar Products]
UniProt Entry Name
CXB6_HUMAN
NCBI Summary for GJB6
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. [provided by RefSeq, Jul 2008]
UniProt Comments for GJB6
GJB6: 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. Belongs to the connexin family. Beta-type (group I) subfamily. A connexon is composed of a hexamer of connexins. Interacts with CNST
Protein type: Membrane protein, multi-pass
Chromosomal Location of Human Ortholog: 13q12
Cellular Component: cell junction
Disease: Clouston Syndrome; Deafness, Autosomal Dominant 3b; Deafness, Autosomal Recessive 1a; Deafness, Autosomal Recessive 1b; Deafness, X-linked 2
Research Articles on GJB6
1. identification and functional characterization of a new Cx30 mutation in a family with hearing impairment in association with previously unreported skin anomalies
Precautions
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Disclaimer
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