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Connexin 26, Polyclonal Antibody

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產品名稱: Connexin 26, Polyclonal Antibody
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Connexin 26, Polyclonal Antibody


Connexin 26, Polyclonal Antibody  的詳細介紹
Product Name

Connexin 26 (CX26), Polyclonal Antibody

Popular Item
Full Product Name

Connexin 26 Antibody

Product Synonym Names
connexin 26; Connexin-26; CXB2_HUMAN; DFNA3; DFNB1; Gap junction beta-2 protein; GJB2; HID; KID; NSRD1; PPK
Product Gene Name

anti-CX26 antibody

[Similar Products]
Product Synonym Gene Name
GJB2[Similar Products]
Research Use Only
For Research Use Only. Not for use in diagnostic procedures.
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3D Structure
ModBase 3D Structure for P29033
Clonality
Polyclonal
Isotype
IgG
Host
Rabbit
Species Reactivity
Human, Mouse, Rat
Specificity
Connexin 26 antibody detects endogenous levels of total Connexin 26
Purity/Purification
The antiserum was purified by peptide affinity chromatography using SulfoLink Coupling Resin.
Form/Format
Liquid
Phosphate buffered saline, pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
Concentration
1mg/ml (lot specific)
Immunogen
A synthesized peptide derived from human Connexin 26
Subcellular Location
Cell Membrane. Cell Junction > Gap Junction.
Predicted Cross Reactivity
Pig, Bovine, Horse, Sheep, Rabbit, Dog
Similarity
Pig (100%), Bovine (91%), Horse (100%), Sheep (91%), Rabbit (100%), Dog (100%)
Conjugation
Unconjugated
Preparation and Storage
Store at -20 degree C. Stable for 12 months from date of receipt.
ISO Certification
Manufactured in an ISO 9001:2015 Certified Laboratory.
Supply Chain Verification
Manufactured in a lab with traceable raw materials manufactured on site. Coordinated product portfolio of antibodies, pairs, conjugates, recombinant proteins, and immunoassay materials available, please inquire.
Other Notes
Small volumes of anti-CX26 antibody 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.
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Related Product Information for
anti-CX26 antibody
Description: A form of non-syndromic sensorineural hearing loss. Sensorineural deafness results from damage to the neural receptors of the inner ear, the nerve pathways to the brain, or the area of the brain that receives sound information. Note: The disease is caused by mutations affecting the gene represented in this entry.
Function: 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.
Subunit Structure: A connexon is composed of a hexamer of connexins. Interacts with CNST (By similarity).
Similarity: Belongs to the connexin family. Beta-type (group I) subfamily.
Applications Tested/Suitable for anti-CX26 antibody
Western Blot (WB), Immunohistochemistry (IHC), ELISA (EIA)
Application Notes for anti-CX26 antibody
WB: 1:500-1:2000
IHC: 1:200

Immunohistochemistry (IHC) of anti-CX26 antibody
MBS9601289 at 1/100 staining Mouse intestine tissue by IHC-P. The sample was formaldehyde fixed and a heat mediated antigen retrieval step in citrate buffer was performed. The sample was then blocked and incubated with the antibody for 1.5 hours at 22 degree C. An HRP conjugated goat anti-rabbit antibody was used as the secondary.
anti-CX26 antibody Immunohistochemistry (IHC) (IHC) image
Western Blot (WB) of anti-CX26 antibody
Western blot analysis of Connexin 26 expression in Jurkat cells, The lane on the left is treated with the antigen-specific peptide.
anti-CX26 antibody Western Blot (WB) (WB) image
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NCBI/Uniprot data below describe general gene information for CX26. It may not necessarily be applicable to this product.
NCBI GI #
42558283
NCBI GeneID
2706
NCBI Accession #
NP_003995.2 [Other Products]
NCBI GenBank Nucleotide #
NM_004004.5 [Other Products]
UniProt Primary Accession #
P29033 [Other Products]
UniProt Secondary Accession #
Q508A5; Q508A6; Q5YLL0; Q5YLL1; Q5YLL4; Q6IPV5; Q86U88; Q96AK0; Q9H536; Q9NNY4[Other Products]
UniProt Related Accession #
P29033[Other Products]
Molecular Weight
Observed: 26 kDa
Predicted: 27 kDa
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NCBI Official Full Name
gap junction beta-2 protein
NCBI Official Synonym Full Names
gap junction protein beta 2
NCBI Official Symbol
GJB2??[Similar Products]
NCBI Official Synonym Symbols
HID; KID; PPK; CX26; DFNA3; DFNB1; NSRD1; DFNA3A; DFNB1A
??[Similar Products]
NCBI Protein Information
gap junction beta-2 protein
UniProt Protein Name
Gap junction beta-2 protein
UniProt Synonym Protein Names
Connexin-26; Cx26
UniProt Gene Name
GJB2??[Similar Products]
UniProt Synonym Gene Names
Cx26??[Similar Products]
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NCBI Summary for CX26
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]
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UniProt Comments for CX26
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.CautionThe Thr-34 allele was originally thought to be a cause of autosomal dominant and recessive deafness (DFNA3 and DFNB1) (PubMed:9139825). However, Thr-34 effect on hearing is controversial. Some studies supports its pathogenic role (PubMed:17935238 and PubMed:16849369). Others provide evidence of the non-pathogenic nature of this variant (PubMed:9422505 and PubMed:14694360).
Research Articles on CX26
1. It was shown that thiol levels increased and disulphide levels decreased in patients with autosomal recessive non-syndromic hearing loss and GJB2 gene mutations.
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Precautions
All of MyBioSource's Products are for scientific laboratory research purposes and are not for diagnostic, therapeutics, prophylactic or in vivo use. Through your purchase, you expressly represent and warrant to MyBioSource that you will properly test and use any Products purchased from MyBioSource in accordance with industry standards. MyBioSource and its authorized distributors reserve the right to refuse to process any order where we reasonably believe that the intended use will fall outside of our acceptable guidelines.
Disclaimer
While every efforts were made to ensure the accuracy of the information provided in this datasheet, MyBioSource will not be liable for any omissions or errors contained herein. MyBioSource reserves the right to make changes to this datasheet at any time without prior notice.

It is the responsibility of the customer to report product performance issues to MyBioSource within 30 days of receipt of the product. Please visit our Terms & Conditions page for more information.
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