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Invitrogen
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This antibody is tested in Peptide ELISA: antibody detection limit dilution 1,000.
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: Cadherin; cadherin 23; Cadherin-23; cadherin-like 23; cadherin-related family member 23; DFNB12; DKFZp434P2350; FLJ00233; FLJ36499; MGC102761; Otocadherin; OTTHUMP00000044780; USH1H
基因别名: CDH23; CDHR23; KIAA1774; KIAA1812; UNQ1894/PRO4340; USH1D
UniProt ID: (Human) Q6UWW1
Entrez Gene ID: (Human) 64072