
Thermo Fisher Scientific Connexin 26 Polyclonal Antibody
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Applications
Tested Dilution
Publications
Western Blot (WB)
0.01-1 µg/mL
Immunohistochemistry (IHC)
-
View 1 publication 1 publication
Flow Cytometry (Flow)
10 µg/mL
Product Specifications
Species Reactivity
Human, Mouse, Rat
Published species
Not Applicable
Host/Isotype
Goat / IgG
Class
Polyclonal
Type
Antibody
Immunogen
Synthetic peptide sequence (YLLIRYCSGKSKKP) corresponding to the C-terminus amino acids of GJB2 (aa 212-225). if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
Connexin 26,
uniProtId:
P29033-1,
ncbiNodeId:
9606,
antigenRange:
212-225,
antigenLength:
226,
antigenImageFileName:
PA5-18618_Connexin_26_P29033-1_Goat.svg,
antigenImageFileNamePDP:
PA5-18618_Connexin_26_P29033-1_Goat_PDP.jpeg,
sortOrder:
1}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
Ammonium sulfate precipitation
Storage buffer
TBS, pH 7.3, with 0.5% BSA
Contains
0.02% sodium azide
Storage conditions
-20° C, Avoid Freeze/Thaw Cycles
Shipping conditions
Wet ice
RRID
AB_10982506
Product Specific Information
This antibody is predicted to react with human and rat based on sequence homology.
This antibody is tested in Peptide ELISA: antibody detection limit dilution 128,000.
Target Information
Gap junctions are conduits that allow the direct cell-to-cell passage of small cytoplasmic molecules, including ions, metabolic intermediates, and second messengers, and thereby mediate intercellular metabolic and electrical communication. Gap junction channels consist of connexin protein subunits, which are encoded by a multigene family. GJBs (gap-junction proteins or connexins) play crucial functional roles associated with these channels. Defects in GJB3 have been linked to erythrokeratodermia variables (EKV) is an autosomal dominant genodermatosis characterized by transient figurate red patches or hyperkeratosis. Mutations in GJB2 have also been associated with genetically derived hearing impairments, including autosomal recessive nonsyndromic deafness.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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