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Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1) ELISA Kits

RP1 encodes a member of the doublecortin family. Additionally we are shipping RP1 Antibodies (13) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Human RP1 RP1 6101 P56715
Anti-Rat RP1 RP1 681377  
Anti-Mouse RP1 RP1 19888 P56716
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More ELISA Kits for RP1 Interaction Partners

Human Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1) interaction partners

  1. The L66P mutation in the first doublecortin (show DCX ELISA Kits) domain of the Rp1 (show STK19 ELISA Kits) gene impairs Rp1 (show STK19 ELISA Kits) protein localization and function, leading to abnormalities in photoreceptor outer segment structure and progressive photoreceptor degeneration.

  2. We suggest that arRP patients with high myopic refractive error should be preferentially analysed for RP1 (show STK19 ELISA Kits) mutations.

  3. it reports that different regions of RP1 (show STK19 ELISA Kits) can also lead to arRCD.

  4. Two novel heterozygous null mutations in RP1 (show STK19 ELISA Kits) co-segregate with the disease in autosomal recessive retinitis pigmentosa patients.

  5. RP1 (show STK19 ELISA Kits) phosphorylation at Ser (show SIGLEC1 ELISA Kits)(236) by CK2 (show CSNK2A1 ELISA Kits) seems to play a significant role in cell adhesion and might initiate new insights in the CK2 (show CSNK2A1 ELISA Kits) and EB1 (show MAPRE2 ELISA Kits) family protein association.

  6. Data found pathogenic DNA variants in the genes RP1 (show STK19 ELISA Kits), USH2A (show USH2A ELISA Kits), CNGB3 (show CNGB3 ELISA Kits), NMNAT1 (show NMNAT1 ELISA Kits), CHM (show CHM ELISA Kits), and ABCA4 (show ABCA4 ELISA Kits), responsible for retinitis pigmentosa, Usher syndrome, achromatopsia, Leber congenital amaurosis, choroideremia (show CHM ELISA Kits), or recessive Stargardt/cone-rod dystrophy cases.

  7. The most severe missense mutation occurred in patients with p.D984G in RP1 (show STK19 ELISA Kits).

  8. A novel homozygous retinitis pigmentosa nonsense mutation in exon 4 of the RP1 (show STK19 ELISA Kits) gene, c.1012C>T (p.R338*) was identified in the proband and her two affected sisters.

  9. molecular mechanism of RP1 (show STK19 ELISA Kits) mutation

  10. The distribution of these novel and previously reported RP1 (show STK19 ELISA Kits) mutations makes it challenging to describe a unifying mutational mechanism for dominant versus recessive RP1 (show STK19 ELISA Kits)-related retinitis pigmentosa.

Mouse (Murine) Retinitis Pigmentosa 1 (Autosomal Dominant) (RP1) interaction partners

  1. The L66P mutation in the first doublecortin (show DCX ELISA Kits) domain of the Rp1 gene impairs Rp1 protein localization and function, leading to abnormalities in photoreceptor outer segment structure and progressive photoreceptor degeneration.

  2. RP1 is required for the correct orientation and higher order stacking of outer segment discs.

  3. RP1 is a photoreceptor-specific microtubule-associated protein (show SPAG5 ELISA Kits) that participates in controlling the length and stability of the photoreceptor axoneme.

  4. The disruption of Rp1 changed gene expression in the c-Jun N-terminal kinase signaling cascades.

  5. Rp1 and Rp1L1 (show RP1L1 ELISA Kits) play essential and synergistic roles in affecting photosensitivity and morphogenesis of rod photoreceptors. Our findings suggest that mutations in RP1L1 (show RP1L1 ELISA Kits) could underlie retinopathy or modify RP1 disease expression

RP1 Antigen Profile

Antigen Summary

This gene encodes a member of the doublecortin family. The protein encoded by this gene contains two doublecortin domains, which bind microtubules and regulate microtubule polymerization. The encoded protein is a photoreceptor microtubule-associated protein and is required for correct stacking of outer segment disc. This protein and the RP1L1 protein, another retinal-specific protein, play essential and synergistic roles in affecting photosensitivity and outer segment morphogenesis of rod photoreceptors. Because of its response to in vivo retinal oxygen levels, this protein was initially named ORP1 (oxygen-regulated protein-1). This protein was subsequently designated RP1 (retinitis pigmentosa 1) when it was found that mutations in this gene cause autosomal dominant retinitis pigmentosa. Mutations in this gene also cause autosomal recessive retinitis pigmentosa. Two transcript variants encoding distinct isoforms are resulted from alternative promoters and alternative splicing.

Gene names and symbols associated with RP1

  • retinitis pigmentosa 1 (autosomal dominant) (rp1) antibody
  • retinitis pigmentosa 1 (autosomal dominant) (RP1) antibody
  • retinitis pigmentosa 1 (human) (Rp1) antibody
  • Dcdc3 antibody
  • DCDC4A antibody
  • mG145 antibody
  • MGC83581 antibody
  • Orp1 antibody
  • Rp1h antibody

Protein level used designations for RP1

retinitis pigmentosa 1 (autosomal dominant) , retinitis pigmentosa RP1 protein , oxygen-regulated protein 1-like , oxygen-regulated protein 1 , retinitis pigmentosa 1 protein , retinitis pigmentosa RP1 protein homolog , retinitis pigmentosa 1 homolog

GENE ID SPECIES
447052 Xenopus laevis
472766 Pan troglodytes
677695 Macaca mulatta
100053179 Equus caballus
100188920 Xenopus (Silurana) tropicalis
100355685 Oryctolagus cuniculus
100444488 Pongo abelii
6101 Homo sapiens
280916 Bos taurus
403565 Canis lupus familiaris
681377 Rattus norvegicus
19888 Mus musculus
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