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  2. Polyclonal

GTX17229

Connexin 26 antibody

Cannot supply to this region.

SKU:
GTX17229
Additional Names:
gap junction protein beta 2 , CX26 , DFNA3 , DFNA3A , DFNB1 , DFNB1A , HID , KID , NSRD1 , PPK
Application:
ELISA, WB
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human
Buffer:
PBS, 0.02% Sodium azide.
Immunogen:
Connexin 26 antibody was raised against a 16 amino acid peptide near the center of human Connexin 26.The immunogen is located within amino acids 80 - 130 of Connexin 26.
Uniprot:
P29033
Synonyms:
BAPS;connexin 26;Connexin-26;CX26;DFNA3;DFNA3A;DFNB1;DFNB1A;gap junction beta 2 proteinc;gap junction beta-2 protein;gap junction protein, beta 2, 26kDa;HID;KID;mutant gap junction beta 2 protein;mutant gap junction protein beta 2;NSRD1;PPK
Extra Details:
This gene encodes a member of the gap junction protein family. The gap junctions were first characterized by electron microscopy as regionally specialized structures on plasma membranes of contacting adherent cells. These structures were shown to consist of cell-to-cell channels that facilitate the transfer of ions and small molecules between cells. The gap junction proteins, also known as connexins, purified from fractions of enriched gap junctions from different tissues differ. According to sequence similarities at the nucleotide and amino acid levels, the gap junction proteins are divided into two categories, alpha and beta. Mutations in this gene are responsible for as much as 50% of pre-lingual, recessive deafness. [provided by RefSeq, Oct 2008]
Shipping Conditions:
Blue Ice