Human ATP Binding Cassette Transporter A4 (ABCA4) ELISA Kit (96T)

Human ATP Binding Cassette Transporter A4 (ABCA4) ELISA Kit (96T)

Catalog #: TD3028
Availability: In Stock
¥649.00
Detection range: 0.312-20ng/mL    
Sensitivity: 0.112ng/mL    
Type: Traditional ABCA4 ELISA kit    
Synonyms: ABC-A4; ABC10; ABCR; ARMD2; CORD3; FFM; RMP; RP19; STGD; STGD1; Stargardt disease protein; Retinal-specific ATP-binding cassette transporter; RIM ABC transporter
Species: Human
Sample type: tissue homogenates, cell lysates or other biological fluids.
Experimental method: Sandwich
Shelf life: 12 months
Gene ID: 24
UniProt ID: P78363
Components: 1. Pre-coated, ready to use 96-well strip plate 1
2. Plate sealer for 96 wells 2
3. Standard 2
4. Diluents buffer: 1×45 mL
5. Detection Reagent A: 1×120 μL
6. Detection Reagent B: 1×120 μL
7. TMB Substrate: 1×9 mL
8. Stop Solution: 1×6 mL
9. Wash Buffer (30× concentrate): 1×20 mL




Background

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, and the gene product mediates transport of an essental molecule, all-trans-retinal aldehyde (atRAL), 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.

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ABCA4