Protocadherin 21 (PCDH24) Kits ELISA

PCDH24 is a member of the cadherin superfamily of calcium-dependent cell-cell adhesion molecules. De plus, nous expédions Protocadherin 21 Anticorps (24) et Protocadherin 21 Protéines (9) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
PCDH24 92211 Q96JP9
PCDH24 170677 Q8VHP6
PCDH24 93662 Q91XU7
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Top Protocadherin 21 Kits ELISA sur

Showing 5 out of 9 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Livraison Prix Détails
Humain 0.16 ng/mL n/a   96 Tests 15 to 18 Days
Souris < 46.9 pg/mL 78 pg/mL - 5000 pg/mL   96 Tests 11 to 18 Days
Rat < 0.094 ng/mL 0.156 ng/mL - 10 ng/mL   96 Tests 11 to 18 Days
Boeuf (Vache)
  96 Tests 15 to 18 Days
  96 Tests 15 to 18 Days

Plus Kits ELISA pour Protocadherin 21 partenaires d'interaction

Human Protocadherin 21 (PCDH24) interaction partners

  1. Mutations in CDHR1 are a rare cause of retinal dystrophy. This study further expands the mutational spectrum of this gene and the associated clinical presentation.

  2. CDHR1-related retinal dystrophy should be considered in adult patients with a retinal dystrophy who present with symptoms of cone-and-rod dysfunction and macular atrophy on ophthalmoscopic examination.

  3. the recessive retinal disorder previously reported to be due to homozygous mutation in RGR is, at least in part, due to variants in CDHR1 and that the true consequences of RGR knock-out on human retinal structure and function are yet to be determined.

  4. we delineate the retinal pathology of two families segregating autosomal recessive retinal dystrophy due to two previously undescribed mutations in CDHR1.

  5. Lack of CDHR1 in the human retina causes symptoms related to cone photoreceptor dysfunction.

  6. A novel splice site mutation of CDHR1, c.1485+2T>G, underlying autosomal recessive cone-rod dystrophy has been described in a consanguineous Israeli Christian Arab family.

  7. High-resolution retinal imaging revealed outer retinal changes suggesting that CDHR1 is important for normal photoreceptor structure and survival.

  8. To our knowledge, this is the first report of mutations in PCDH21 as a cause of human disease, autosomal recessive cone-rod dystrophy.

  9. Biallelic mutations in the photoreceptor-specific gene PCDH21 cause recessive retinal degeneration in humans.

  10. PCDH21 mutations are not a major cause of the retinal diseases investigated herein, and the corresponding human phenotype remains to be determined.

Mouse (Murine) Protocadherin 21 (PCDH24) interaction partners

  1. Data indicate junctions between the inner segment (IS) and the outer segment (OS) that contain the photoreceptor-specific cadherin, PCDH21 (pr-CAD).

  2. prCAD ectodomain cleavage is an integral part of the outer segment assembly process, and outer segment assembly might be driven, at least in part, by the near irreversibility of proteolysis.

Protocadherin 21 (PCDH24) profil antigène

Antigen Summary

This gene is a member of the cadherin superfamily of calcium-dependent cell-cell adhesion molecules. This non-classical cadherin appears to be exclusively expressed in the mitral and tufted cells in the main and accessory olfactory bulbs of the brain, suggesting a possible role in the formation and maintenance of neuronal networks. Alternatively spliced transcript variants encoding different isoform have been identified.

Gene names and symbols associated with Protocadherin 21 (PCDH24) Kits ELISA

  • cadherin related family member 1 (CDHR1) anticorps
  • cadherin-related family member 1 (Cdhr1) anticorps
  • cadherin related family member 1 L homeolog (cdhr1.L) anticorps
  • CORD15 anticorps
  • mKIAA1775 anticorps
  • pcdh21 anticorps
  • prCAD anticorps
  • RP65 anticorps

Protein level used designations for Protocadherin 21 (PCDH24) Kits ELISA

MT-protocadherin , photoreceptor cadherin , protocadherin-21 , protocadherin 21 , prCAD , photoreceptor protocadherin , Protocadherin-21

92211 Homo sapiens
170677 Mus musculus
93662 Rattus norvegicus
281996 Bos taurus
414847 Gallus gallus
100337587 Xenopus laevis
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