PRPH2 Antibody (N-term) Blocking peptide
€363.00
In stock
SKU
AC-BP12554a
Background:
The protein encoded by this gene is a member of thetransmembrane 4 superfamily, also known as the tetraspanin family.Most of these members are cell-surface proteins that arecharacterized by the presence of four hydrophobic domains. Theproteins mediate signal transduction events that play a role in theregulation of cell development, activation, growth and motility.This encoded protein is a cell surface glycoprotein found in theouter segment of both rod and cone photoreceptor cells. It mayfunction as an adhesion molecule involved in stabilization andcompaction of outer segment disks or in the maintenance of thecurvature of the rim. This protein is essential for diskmorphogenesis. Defects in this gene are associated with bothcentral and peripheral retinal degenerations. Some of the variousphenotypically different disorders are autosomal dominant retinitispigmentosa, progressive macular degeneration, macular dystrophy andretinitis pigmentosa digenic.
Other Names:
Peripherin-2, Retinal degeneration slow protein, Tetraspanin-22, Tspan-22, PRPH2, PRPH, RDS, TSPAN22
Gene Name: PRPH2
Gene ID: 5961
Primary Accession: P23942
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
The protein encoded by this gene is a member of thetransmembrane 4 superfamily, also known as the tetraspanin family.Most of these members are cell-surface proteins that arecharacterized by the presence of four hydrophobic domains. Theproteins mediate signal transduction events that play a role in theregulation of cell development, activation, growth and motility.This encoded protein is a cell surface glycoprotein found in theouter segment of both rod and cone photoreceptor cells. It mayfunction as an adhesion molecule involved in stabilization andcompaction of outer segment disks or in the maintenance of thecurvature of the rim. This protein is essential for diskmorphogenesis. Defects in this gene are associated with bothcentral and peripheral retinal degenerations. Some of the variousphenotypically different disorders are autosomal dominant retinitispigmentosa, progressive macular degeneration, macular dystrophy andretinitis pigmentosa digenic.
Other Names:
Peripherin-2, Retinal degeneration slow protein, Tetraspanin-22, Tspan-22, PRPH2, PRPH, RDS, TSPAN22
Gene Name: PRPH2
Gene ID: 5961
Primary Accession: P23942
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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