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Invitrogen™ CDH23 Polyclonal Antibody
Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5102659
Description
Antibody detects endogenous levels of total CDH23.
This gene is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. The encoded protein is thought to be involved in stereocilia organization and hair bundle formation. The gene is located in a region containing the human deafness loci DFNB12 and USH1D. Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of this cadherin-like gene. Alternative splice variants encoding different isoforms have been described.
Specifications
CDH23 | |
Polyclonal | |
Unconjugated | |
CDH23 | |
4930542A03Rik; age related hearing loss 1; ahl; ahl1; bob; bobby; bus; bustling; Cadherin; cadherin 23; cadherin 23 (otocadherin); cadherin related 23; cadherin-23; cadherin-like 23; cadherin-related 23; cadherin-related family member 23; Cdh23; CDHR23; DFNB12; DKFZp434P2350; FLJ00233; FLJ36499; KIAA1774; KIAA1812; mdfw; MGC102761; modifier of deaf waddler; nmf112; nmf181; nmf252; otocadherin; OTTHUMP00000044780; sals; UNQ1894/PRO4340; USH1D; USH1H; v; W; waltzer; Waltzing | |
Rabbit | |
Affinity Chromatography | |
RUO | |
114102, 22295, 64072 | |
-20°C | |
Liquid |
Immunohistochemistry (Paraffin), Western Blot | |
1 mg/mL | |
PBS with 50% glycerol and 0.02% sodium azide; pH 7.4 | |
P58365, Q99PF4, Q9H251 | |
CDH23 | |
A synthesized peptide derived from human CDH23(Accession Q9H251), corresponding to amino acid residues K445-V495. | |
100 μL | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
Safety and Handling
WARNING: Cancer - www.P65Warnings.ca.gov
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