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Cadherin-Like 23 (CDH23) ELISA Kits

CDH23 is a member of the cadherin superfamily, whose genes encode calcium dependent cell-cell adhesion glycoproteins. Additionally we are shipping CDH23 Antibodies (13) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human CDH23 CDH23 64072 Q9H251
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More ELISA Kits for CDH23 Interaction Partners

Human Cadherin-Like 23 (CDH23) interaction partners

  1. A new diagnosis of sector retinitis pigmentosa was found to have two novel compound heterozygous mutations in CDH23, including one missense (c.8530C > A; p.Pro2844Thr) and one splice-site (c.5820 + 5G > A) mutation.

  2. Four (3.1 %) of 128 children carried two CDH23 mutant alleles, and SLC26A4 (show SLC26A4 ELISA Kits) and GJB2 (show GJB2 ELISA Kits) accounted for 18.0 and 17.2 %, respectively and showed profound nonsyndromic sensorineural hearing loss with minimal residual hearing.

  3. The results revealed that CDH23 mutations are highly prevalent in patients with congenital high-frequency sporadic or recessively inherited hearing loss

  4. Description of the spectrum of mutations in CDH23 in 374 families with autosomal recessive, non-syndromic hearing loss from India.

  5. The results of this study confirm that CDH23 genetic variant may modify the susceptibility to noise-induced hearing loss development in humans

  6. mutations in the CDH23 gene are one of the most important causes of non-syndromic hearing loss in East Asians.

  7. Hearing loss was found to co-segregate with locus-specific STR (show STATH ELISA Kits) markers for CDH23 in 1 Pakistani family.

  8. mutations of the CDH23 gene are an important cause of non-syndromic hearing loss.

  9. Large protein assemblies formed by multivalent interactions between cadherin23 and harmonin (show USH1C ELISA Kits) suggest a stable anchorage structure at the tip link of stereocilia

  10. Despite that the Ahl allele of Cdh23 had been implicated with ARHI in mice, we found no positive association of the CDH23 tag SNP in intron 7 with ARHI in Han Chinese.

Zebrafish Cadherin-Like 23 (CDH23) interaction partners

  1. Unlike other vertebrates, cdh23 is not detectable in zebrafish photoreceptors but instead expressed by a small subset of GABAergic amacrine cells.

  2. Cdh23 is an essential tip link component required for hair-cell mechanotransduction

CDH23 Antigen Profile

Antigen Summary

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.

Gene names and symbols associated with Cadherin-Like 23 (CDH23) ELISA Kits

  • cadherin-related 23 (CDH23) antibody
  • cadherin-like 23 (cdh23) antibody
  • cadherin-like 23 (CDH23) antibody
  • cadherin-like 23 (LOC100337921) antibody
  • CDH23 antibody
  • CDHR23 antibody
  • USH1D antibody

Protein level used designations for Cadherin-Like 23 (CDH23) ELISA Kits

cadherin-23 , cadherin-like 23 , cadherin-related family member 23 , otocadherin , cadherin 23 , cadherin related 23 , spu , sputnik , ush1d

64072 Homo sapiens
407978 Danio rerio
423718 Gallus gallus
450516 Pan troglodytes
784716 Bos taurus
100337921 Oryctolagus cuniculus
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