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Progressive Rod-Cone Degeneration (PRCD) ELISA Kits

PRCD is predominantly expressed in the retina, and mutations in PRCD are the cause of autosomal recessive retinal degeneration in both humans and dogs. Additionally we are shipping PRCD Proteins (3) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human PRCD PRCD 768206 Q00LT1
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More ELISA Kits for PRCD Interaction Partners

Human Progressive Rod-Cone Degeneration (PRCD) interaction partners

  1. The identification of a third mutation in PRCD confirms its role in the pathogenesis of retinitis pigmentosa.

  2. The identification of a second pathogenic mutation of PRCD in multiple retinitis pigmentosa (RP) patients confirms the role of PRCD in the aetiology of RP in humans.

PRCD Antigen Profile

Antigen Summary

This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene.

Gene names and symbols associated with PRCD

  • progressive rod-cone degeneration (PRCD) antibody
  • RP36 antibody

Protein level used designations for PRCD

progressive rod-cone degeneration protein

GENE ID SPECIES
768206 Homo sapiens
100049006 Canis lupus familiaris
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