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Interphotoreceptor matrix proteoglycan

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May interact with hyaluronan which may serve to form a basic macromolecular scaffold comprising the insoluble interphotoreceptor matrix.

Below are the list of possible Interphotoreceptor matrix proteoglycan 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.
 

Interphotoreceptor matrix proteoglycan 1

 Interphotoreceptor matrix proteoglycan 1 ELISA Kit
 Interphotoreceptor matrix proteoglycan 1 Recombinant
 Interphotoreceptor matrix proteoglycan 1 Antibody
Also known as Interphotoreceptor matrix proteoglycan 1 (Interphotoreceptor matrix proteoglycan of 150 kDa) (IPM-150) (Sialoprotein associated with cones and rods).
IMPG1: May interact with hyaluronan which may serve to form a basic macromolecular scaffold comprising the insoluble interphotoreceptor matrix.

Protein type: Secreted; Secreted, signal peptide

Chromosomal Location of Human Ortholog: 6q14.2-q15

Cellular Component: proteinaceous extracellular matrix

Molecular Function: extracellular matrix structural constituent

Biological Process: visual percepti
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on

Disease: Macular Dystrophy, Vitelliform, 4
 IMPG1 ELISA Kit
 IMPG1 Recombinant
 IMPG1 Antibody
 IPM150 ELISA Kit
 IPM150 Recombinant
 IPM150 Antibody
 SPACR ELISA Kit
 SPACR Recombinant
 SPACR Antibody
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Interphotoreceptor matrix proteoglycan 2

 Interphotoreceptor matrix proteoglycan 2 ELISA Kit
 Interphotoreceptor matrix proteoglycan 2 Recombinant
 Interphotoreceptor matrix proteoglycan 2 Antibody
Also known as Interphotoreceptor matrix proteoglycan 2 (Interphotoreceptor matrix proteoglycan of 200 kDa) (IPM 200) (Sialoprotein associated with cones and rods proteoglycan) (Spacrcan).
IMPG2: Chondroitin sulfate- and hyaluronan-binding proteoglycan involved in the organization of interphotoreceptor matrix; may participate in the maturation and maintenance of the light- sensitive photorecepto
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r outer segment. Binds heparin. Defects in IMPG2 are the cause of retinitis pigmentosa type 56 (RP56). RP56 is a retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well. Defects in IMPG2 are the cause of maculopathy IMPG2- related (MACLP-IMPG2). MACLP-IMPG2 is a mild maculopathy characterized by full-field electroretinogram responses within normal limits, normal color vision, elevation of the photoreceptor layer in the foveal region and mild nuclear sclerosis.

Protein type: Extracellular matrix; Membrane protein, integral

Chromosomal Location of Human Ortholog: 3q12.2-q12.3

Cellular Component: proteinaceous extracellular matrix; receptor complex

Molecular Function: extracellular matrix structural constituent; hyaluronic acid binding

Biological Process: visual perception

Disease: Macular Dystrophy, Vitelliform, 5; Retinitis Pigmentosa 56
 IMPG2 ELISA Kit
 IMPG2 Recombinant
 IMPG2 Antibody
 IPM200 ELISA Kit
 IPM200 Recombinant
 IPM200 Antibody
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