Anti-Human/Mouse/Rat Otocadherin Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12570
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human CDH23
Specificity Particularly strong expression in the retina. Found also in the cochlea.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot Q9H251
Concentration 0.1 mg/mL
Dilution IHC 1:50-1:200
Formulation
Application IHC,ELISA
Other Names Age related hearing loss 1,Ahl 1,Ahl,Ahl1,Bob,Bobby,Bus,Bustling,Cadherin 23,Cadherin23,CDH 23,Mdfw,Modifier of deaf waddler,nmf112,nmf181,nmf252,Otocadherin,USH 1D,USH1 D,USH1D,Waltzer
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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