Protocadherin 21 (PCDH24) ELISA Kits

PCDH24 is a member of the cadherin superfamily of calcium-dependent cell-cell adhesion molecules. Zusätzlich bieten wir Ihnen Protocadherin 21 Antikörper (27) und Protocadherin 21 Proteine (9) und viele weitere Produktgruppen zu diesem Protein an.

list all ELISA KIts Gen GeneID UniProt
PCDH24 92211 Q96JP9
PCDH24 170677 Q8VHP6
PCDH24 93662 Q91XU7
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Top Protocadherin 21 ELISA Kits auf antikoerper-online.de

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Katalog Nr. Reaktivität Sensitivität Bereich Bilder Menge Anbieter Lieferzeit Preis Details
Human 0.16 ng/mL   96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
772,39 €
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Maus
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
788,70 €
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Ratte
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
788,70 €
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Rind (Kuh)
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
945,85 €
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Huhn
  96 Tests Anmelden zum Anzeigen 13 bis 17 Tage
1.013,20 €
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Weitere ELISA Kits für Protocadherin 21 Interaktionspartner

Human Protocadherin 21 (PCDH24) Interaktionspartner

  1. 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.

  2. we delineate the retinal pathology of two families segregating autosomal recessive retinal dystrophy (zeige MERTK ELISA Kits) due to two previously undescribed mutations in CDHR1.

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

  4. 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.

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

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

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

  8. 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) Interaktionspartner

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

  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) Antigen-Profil

Beschreibung des Gens

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.

Genbezeichner und Symbole assoziert mit Protocadherin 21 (PCDH24) ELISA Kits

  • cadherin-related family member 1 (CDHR1) Antikörper
  • cadherin-related family member 1 (Cdhr1) Antikörper
  • cadherin-related family member 1 (cdhr1) Antikörper
  • CORD15 Antikörper
  • mKIAA1775 Antikörper
  • pcdh21 Antikörper
  • prCAD Antikörper
  • RP65 Antikörper

Bezeichner auf Proteinebene für Protocadherin 21 (PCDH24) ELISA Kits

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

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