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Cadherin 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 (54) and CDH23 Proteins (5) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Mouse CDH23 CDH23 22295 Q99PF4
Anti-Human CDH23 CDH23 64072 Q9H251
Anti-Rat CDH23 CDH23 114102 P58365
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More ELISA Kits for CDH23 Interaction Partners

Mouse (Murine) Cadherin 23 (CDH23) interaction partners

  1. Our results showed that systemic treatment with TUDCA significantly alleviated hearing loss and suppressed hair cell death in erl(Cdh23) mice. Additionally.

  2. This study further resolves the interaction between Atp2b2 (show ATP2B2 ELISA Kits) and Cdh23 in a gene dosage and frequency-dependent manner, and finds that low auditory frequencies are significantly affected by the interaction.

  3. crystallography, molecular dynamics simulations and binding experiments to characterize the protocadherin 15 (show PCDH15 ELISA Kits)-cadherin 23 bond

  4. A point mutation in the Cdh23 gene (208T>C) of C57BL/6J mice results in hearing loss around 1 month after birth.

  5. the Cdh23(nmf308/nmf308) mice with progressive hair cell loss had specific morphological changes and suffered a base to apex gradient and age-related hearing loss (AHL), and that mutations in cdh23 were linked to AHL

  6. A novel synaptic Usher complex comprised of clarin-1 and specific isoforms of CDH23, PCDH15 and VLGR1, was identified.

  7. Although Cdh23(ahl) homozygosity is necessary, it is not by itself sufficient to account for the accelerated hearing loss of C57BL/6J mice.

  8. ENU-induced mutation of Cdh23 causes congenital hearing loss, but no vestibular dysfunction, in mice

  9. results therefore provide genetic evidence consistent with PCDH15 (show PCDH15 ELISA Kits) and CDH23 being part of the tip-link complex and necessary for normal mechanotransduction

  10. Cadherin-23, myosin VIIa (show MYO7A ELISA Kits) and harmonin (show USH1C ELISA Kits) form a ternary complex and interact with phospholipids.

Human Cadherin 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.

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 23 (CDH23) ELISA Kits

  • cadherin 23 (otocadherin) (Cdh23) antibody
  • cadherin-related 23 (CDH23) antibody
  • cadherin-related 23 (Cdh23) antibody
  • 4930542A03Rik antibody
  • ahl antibody
  • ahl1 antibody
  • bob antibody
  • bus antibody
  • CDHR23 antibody
  • mdfw antibody
  • nmf112 antibody
  • nmf181 antibody
  • nmf252 antibody
  • sals antibody
  • USH1D antibody
  • v antibody
  • W antibody

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

age related hearing loss 1 , bobby , bustling , cadherin-23 , modifier of deaf waddler , otocadherin , waltzer , cadherin-like 23 , cadherin-related family member 23 , Waltzing , cadherin 23 (otocadherin) , cadherin related 23

22295 Mus musculus
64072 Homo sapiens
114102 Rattus norvegicus
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