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Retinitis pigmentosa 9 protein

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Is thought to be a target protein for the PIM1 kinase. May play some roles in B-cell proliferation in association with PIM1 (By similarity).

Below are the list of possible Retinitis pigmentosa 9 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 9 protein

 Retinitis pigmentosa 9 protein ELISA Kit
 Retinitis pigmentosa 9 protein Recombinant
 Retinitis pigmentosa 9 protein Antibody
Also known as Retinitis pigmentosa 9 protein (Pim-1-associated protein) (PAP-1).
RP9: Is thought to be a target protein for the PIM1 kinase. May play some roles in B-cell proliferation in association with PIM1. Defects in RP9 are the cause of retinitis pigmentosa type 9 (RP9). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and loss of mid
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peripheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP9 inheritance is autosomal dominant.

Protein type: RNA processing

Chromosomal Location of Human Ortholog: 7p14.3

Cellular Component: cytoplasm; nucleus

Molecular Function: protein binding

Biological Process: cognition; RNA splicing

Disease: Retinitis Pigmentosa 9
 RP9 ELISA Kit
 RP9 Recombinant
 RP9 Antibody
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Retinitis pigmentosa 9 protein homolog

 Retinitis pigmentosa 9 protein homolog ELISA Kit
 Retinitis pigmentosa 9 protein homolog Recombinant
 Retinitis pigmentosa 9 protein homolog Antibody
Also known as Retinitis pigmentosa 9 protein homolog (Pim-1-associated protein) (PAP-1).
RP9: Is thought to be a target protein for the PIM1 kinase. May play some roles in B-cell proliferation in association with PIM1. Defects in RP9 are the cause of retinitis pigmentosa type 9 (RP9). RP leads to degeneration of retinal photoreceptor cells. Patients typically have night vision blindness and los
>>>
s of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. RP9 inheritance is autosomal dominant.

Protein type: RNA processing

Cellular Component: cytoplasm; nuclear speck; nucleus; signal recognition particle receptor complex

Molecular Function: protein binding

Biological Process: cognition
 rp9 ELISA Kit
 rp9 Recombinant
 rp9 Antibody
 Rp9h ELISA Kit
 Rp9h Recombinant
 Rp9h Antibody
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