Recombinant Human ABCA4 protein
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Recombinant Human ABCA4 protein is a Human Fragment protein, in the 2174 to 2273 aa range, expressed in Wheat germ, suitable for SDS-PAGE, ELISA, WB.
View Alternative Names
ABCR, ABCA4, Retinal-specific phospholipid-transporting ATPase ABCA4, ATP-binding cassette sub-family A member 4, RIM ABC transporter, Retinal-specific ATP-binding cassette transporter, Stargardt disease protein, RIM proteinv, RmP
- SDS-PAGE
Unknown
SDS-PAGE - Recombinant Human ABCA4 protein (AB114660)
SDS-PAGE analysis of ab114660 on a 12.5% gel stained with Coomassie Blue.
Reactivity data
Sequence info
Properties and storage information
Shipped at conditions
Appropriate short-term storage conditions
Appropriate long-term storage conditions
Aliquoting information
Storage information
Supplementary information
This supplementary information is collated from multiple sources and compiled automatically.
Biological function summary
ABCA4 has an important function in the clearance of retinal pigments and it operates as part of a larger complex with other visual cycle proteins. Its activity prevents the accumulation of toxic substances that can damage photoreceptors. ABCA4's transport activity is ATP-dependent meaning it requires energy from ATP hydrolysis to perform its duties. This energy consumption highlights the protein's dynamic role in retinal health and visual processes.
Pathways
ABCA4 is an important component in the visual cycle and the retinoid cycle pathway in rods and cones. These pathways are vital for regenerating visual pigments and ensuring proper vision. ABCA4 works alongside related proteins like RPE65 and RDH12 both of which also contribute to retinoid processing and photoreceptor function. The proper flow of retinoids and prevention of toxic buildup depend heavily on ABCA4 and these associated proteins.
Specifications
Form
Liquid
General info
Function
Flippase that catalyzes in an ATP-dependent manner the transport of retinal-phosphatidylethanolamine conjugates like the 11-cis and all-trans isomers of N-retinylidene-phosphatidylethanolamine from the lumen to the cytoplasmic leaflet of photoreceptor outer segment disk membranes, where N-cis-retinylidene-phosphatidylethanolamine (N-cis-R-PE) is then isomerized to its all-trans isomer (N-trans-R-PE) and reduced by RDH8 to produce all-trans-retinol (all-trans-rol) and therefore prevents the accumulation of excess of 11-cis-retinal and its schiff-base conjugate and the formation of toxic bisretinoid (PubMed : 10075733, PubMed : 20404325, PubMed : 22735453, PubMed : 23144455, PubMed : 24097981, PubMed : 29847635, PubMed : 33375396). May display both ATPase and GTPase activity that is strongly influenced by the lipid environment and the presence of retinoid compounds (PubMed : 22735453). Binds the unprotonated form of N-retinylidene-phosphatidylethanolamine with high affinity in the absence of ATP, and ATP binding and hydrolysis induce a protein conformational change that causes the dissociation of N-retinylidene-phosphatidylethanolamine (By similarity).
Sequence similarities
Belongs to the ABC transporter superfamily. ABCA family.
Post-translational modifications
Proteolytic cleavage by trypsin leads to a 120-kDa N-terminal fragment and a 115-kDa C-terminal fragment that are linked through disulfide bonds.. N-glycosylated.. Phosphorylation is independent of light exposure and modulates ATPase activity.
Target data
Product promise
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