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Retinitis pigmentosa 1-like 1 protein

Required for the differentiation of photoreceptor cells. Plays a role in the organization of outer segment of rod and cone photoreceptors (By similarity).

Below are the list of possible Retinitis pigmentosa 1-like 1 protein products. If you cannot find the target and/or product is not available in our catalog, please click here to contact us and request the product or submit your request for custom elisa kit production, custom recombinant protein production or custom antibody production. Custom ELISA Kits, Recombinant Proteins and Antibodies can be designed, manufactured and produced according to the researcher's specifications.

Retinitis pigmentosa 1-like 1 protein

 Retinitis pigmentosa 1-like 1 protein ELISA Kit
 Retinitis pigmentosa 1-like 1 protein Recombinant
 Retinitis pigmentosa 1-like 1 protein Antibody
RP1L1: Required for the differentiation of photoreceptor cells. Plays a role in the organization of outer segment of rod and cone photoreceptors. Defects in RP1L1 are the cause of occult macular dystrophy (OCMD). An inherited macular dystrophy characterized by progressive loss of macular function but normal ophthalmoscopic appearance. It is typically characterized by a central cone dysfunction lea
ding to a loss of vision despite normal ophthalmoscopic appearance, normal fluorescein angiography, and normal full-field electroretinogram (ERGs), but the amplitudes of the focal macular ERGs and multifocal ERGs are significantly reduced at the central retina. 2 isoforms of the human protein are produced by alternative splicing.

Protein type: Unknown function

Chromosomal Location of Human Ortholog: 8p23.1

Cellular Component: axoneme; photoreceptor connecting cilium; photoreceptor outer segment

Biological Process: axoneme biogenesis; photoreceptor cell development; photoreceptor cell maintenance; retina development in camera-type eye

Disease: Occult Macular Dystrophy
 RP1L1 Recombinant
 RP1L1 Antibody
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