protein

ABCA4 Immunizing Peptide

MBS425337

0.1 mg

190 USD

Peptide

ABCA4 Immunizing Peptide

ABCA4

ABCA4; ATP-binding cassette, sub-family A (ABC1), member 4; ABC10; ABCR; ARMD2; CORD3; DKFZp781N1972; FFM; FLJ17534; RMP; RP19; STGD; STGD1; ATP binding cassette transporter; ATP-binding cassette, sub-family A member 4; ATP-binding transporter, retina-spe

retinal-specific ATP-binding cassette transporter; Retinal-specific ATP-binding cassette transporter; retinal-specific ATP-binding cassette transporter; ATP binding cassette subfamily A member 4; ATP-binding cassette sub-family A member 4; RIM ABC transporter; RIM protein; RmP; Stargardt disease protein

ABCA4

ABCA4; ABCA4; FFM; RMP; ABCR; RP19; STGD; ABC10; ARMD2; CORD3; STGD1; ABCR; RIM protein; RmP

ABCA4_HUMAN

Human

2273

EPECPGPQLNTGTQ

100ug of dried peptide

Shipped at ambient temperature, store at -20 degree C

105990541

NP_000341.2

NM_000350.2

255,944 Da

ABC Transporters Pathway (83035); ABC Transporters Pathway (436); ABC-family Proteins Mediated Transport Pathway (1269904); Signal Transduction Pathway (1269379); The Canonical Retinoid Cycle In Rods (twilight Vision) Pathway (1269625); Transmembrane Transport Of Small Molecules Pathway (1269903); Visual Phototransduction Pathway (1269623)

The membrane-associated protein encoded by this gene is a member of the superfamily of ATP-binding cassette (ABC) transporters. ABC proteins transport various molecules across extra- and intracellular membranes. ABC genes are divided into seven distinct subfamilies (ABC1, MDR/TAP, MRP, ALD, OABP, GCN20, White). This protein is a member of the ABC1 subfamily. Members of the ABC1 subfamily comprise the only major ABC subfamily found exclusively in multicellular eukaryotes. This protein is a retina-specific ABC transporter with N-retinylidene-PE as a substrate. It is expressed exclusively in retina photoreceptor cells, indicating the gene product mediates transport of an essental molecule across the photoreceptor cell membrane. Mutations in this gene are found in patients diagnosed with Stargardt disease, a form of juvenile-onset macular degeneration. Mutations in this gene are also associated with retinitis pigmentosa-19, cone-rod dystrophy type 3, early-onset severe retinal dystrophy, fundus flavimaculatus, and macular degeneration age-related 2. [provided by RefSeq, Jul 2008]

ABCA4: In the visual cycle, acts as an inward-directed retinoid flipase, retinoid substrates imported by ABCA4 from the extracellular or intradiscal (rod) membrane surfaces to the cytoplasmic membrane surface are all-trans-retinaldehyde (ATR) and N-retinyl-phosphatidyl-ethanolamine (NR-PE). Once transported to the cytoplasmic surface, ATR is reduced to vitamin A by trans- retinol dehydrogenase (tRDH) and then transferred to the retinal pigment epithelium (RPE) where it is converted to 11-cis-retinal. May play a role in photoresponse, removing ATR/NR-PE from the extracellular photoreceptor surfaces during bleach recovery. Defects in ABCA4 are the cause of Stargardt disease type 1 (STGD1). STGD is one of the most frequent causes of macular degeneration in childhood. It is characterized by macular dystrophy with juvenile-onset, rapidly progressive course, alterations of the peripheral retina, and subretinal deposition of lipofuscin-like material. STGD1 inheritance is autosomal recessive. Defects in ABCA4 are the cause of fundus flavimaculatus (FFM). FFM is an autosomal recessive retinal disorder very similar to Stargardt disease. In contrast to Stargardt disease, FFM is characterized by later onset and slowly progressive course. Defects in ABCA4 may be a cause of age-related macular degeneration type 2 (ARMD2). ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid (known as drusen) that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane. Defects in ABCA4 are the cause of cone-rod dystrophy type 3 (CORD3). CORDs are inherited retinal dystrophies belonging to the group of pigmentary retinopathies. CORDs are characterized by retinal pigment deposits visible on fundus examination, predominantly in the macular region, and initial loss of cone photoreceptors followed by rod degeneration. This leads to decreased visual acuity and sensitivity in the central visual field, followed by loss of peripheral vision. Severe loss of vision occurs earlier than in retinitis pigmentosa. Defects in ABCA4 are the cause of retinitis pigmentosa type 19 (RP19). RP leads to degeneration of retinal photoreceptor cells. 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. RP19 is characterized by choroidal atrophy. Inheritance is autosomal recessive. Belongs to the ABC transporter superfamily. ABCA family. Protein type: Membrane protein, integral; Transporter, ABC family; Membrane protein, multi-pass; Transporter. Chromosomal Location of Human Ortholog: 1p22. Cellular Component: integral to plasma membrane; intracellular membrane-bound organelle; membrane. Molecular Function: ATP binding; ATPase activity, coupled to transmembrane movement of substances; eye pigment precursor transporter activity; phospholipid-translocating ATPase activity; transporter activity. Biological Process: lipid transport; phospholipid transfer to membrane; phospholipid translocation; photoreceptor cell maintenance; phototransduction, visible light; retinoid metabolic process; transmembrane transport; transport; visual perception. Disease: Cone-rod Dystrophy 3; Macular Degeneration, Age-related, 2; Retinitis Pigmentosa 19; Stargardt Disease 1

0.1 mg

190 USD