GJB6 polyclonal antibody
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Specification
Product Description
Rabbit polyclonal antibody raised against synthetic peptide of GJB6.
Immunogen
A synthetic peptide (conjugated with KLH) corresponding to N-terminus of human GJB6.
Host
Rabbit
Reactivity
Human
Form
Liquid
Purification
Protein G purification
Recommend Usage
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) (1:50-100)
Western Blot (1:1000)
The optimal working dilution should be determined by the end user.Storage Buffer
In PBS (0.09% sodium azide)
Storage Instruction
Store at 4°C. For long term storage store at -20°C.
Aliquot to avoid repeated freezing and thawing.Note
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Applications
Western Blot (Transfected lysate)
Western blot analysis of GJB6 (arrow) using GJB6 polyclonal antibody (Cat # PAB3591).
293 cell lysates (2 ug/lane) either nontransfected (Lane 1) or transiently transfected with the GJB6 gene (Lane 2).Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Formalin-fixed and paraffin-embedded human cancer tissue reacted with GJB6 polyclonal antibody (Cat # PAB3591) , which was peroxidase-conjugated to the secondary antibody, followed by AEC staining. This data demonstrates the use of this antibody for immunohistochemistry ; clinical relevance has not been evaluated. BC = breast carcinoma.Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections)
Formalin-fixed and paraffin-embedded human prostate carcinomareacted with GJB6 polyclonal antibody (Cat # PAB3591), which was peroxidase-conjugated to the secondary antibody, followed by AEC staining.
This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated. -
Gene Info — GJB6
Entrez GeneID
10804Protein Accession#
O95452Gene Name
GJB6
Gene Alias
CX30, DFNA3, ED2, EDH, HED
Gene Description
gap junction protein, beta 6, 30kDa
Gene Ontology
HyperlinkGene Summary
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
Other Designations
OTTHUMP00000018096|OTTHUMP00000176870|OTTHUMP00000176871|OTTHUMP00000176872|connexin 30|ectodermal dysplasia 2, hidrotic (Clouston syndrome)|gap junction protein, beta 6|gap junction protein, beta 6 (connexin 30)
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Interactome
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Disease
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Publication Reference
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Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells.
Beltramello M, Bicego M, Piazza V, Ciubotaru CD, Mammano F, D'Andrea P.
Biochemical and Biophysical Research Communications 2003 Jun; 305(4):1024.
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Functional studies of human skin disease- and deafness-associated connexin 30 mutations.
Common JE, Becker D, Di WL, Leigh IM, O'Toole EA, Kelsell DP.
Biochemical and Biophysical Research Communications 2002 Nov; 298(5):651.
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A novel connexin 30 mutation in Clouston syndrome.
Smith FJ, Morley SM, McLean WH.
The Journal of Investigative Dermatology 2002 Mar; 118(3):530.
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Permeability and gating properties of human connexins 26 and 30 expressed in HeLa cells.
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