|Western Blot (WB)||1-3 ug/ml|
|Tested Species reactivity||Human|
|Host / Isotype||Goat / IgG|
|Immunogen||Synthetic peptide sequence (YNISLYENVTVGTS ) corresponding to the internal amino acids of CDH23|
|Purification||Antigen affinity chromatography|
|Storage buffer||TBS, pH 7.3, with 0.5% BSA|
|Contains||0.02% sodium azide|
|Storage conditions||-20° C, Avoid Freeze/Thaw Cycles|
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: cadherin 23; cadherin related 23; Cadherin-23; cadherin-like 23; cadherin-related family member 23; CDH23; DFNB12; DKFZp434P2350; FLJ00233; FLJ36499; KIAA1774; KIAA1812; MGC102761; Otocadherin; OTTHUMP00000044780; USH1D; USH1H
Gene Aliases: CDH23; CDHR23; KIAA1774; KIAA1812; UNQ1894/PRO4340; USH1D
UniProt ID: (Human) Q9H251
Entrez Gene ID: (Human) 64072
Molecular Function: cadherin
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