ELISA ABCA4 anti-
Quantity :50µL
Clone Number:
Aliases:ABC 10 antibody; ABC A4 antibody; ABC transporter; retinal-specific antibody; ABC10 antibody; ABCA 4 antibody; abcA4 antibody; ABCA4_ antibody; ABCR antibody; ARMD 2 antibody; ARMD2 antibody; ATP binding cassette 10 antibody; ATP binding cassette sub family A member 4 antibody; ATP binding cassette sub family A member4 antibody; ATP binding cassette transporter antibody; ATP binding cassette transporter retinal specific antibody; ATP binding cassette; sub family A (ABC1); member 4 antibody; ATP binding cassette; sub family A (ABC1); member4 antibody; ATP binding cassette10 antibody; ATP binding transporter; retina specific antibody; ATP-binding cassette sub-family A member 4 antibody; CORD 3 antibody; CORD3 antibody; DKFZp781N1972 antibody; FFM antibody; FLJ17534 antibody; Photoreceptor rim protein antibody; Retina specific ABC transporter antibody; Retinal specific ATP binding cassette transporter antibody; Retinal-specific ATP-binding cassette transporter antibody; RIM ABC transporter antibody; RIM protein antibody; RmP antibody; RP 19 antibody; RP19 antibody; Stargardt disease protein antibody; STGD antibody; STGD1 antibody
Product Type:Polyclonal Antibody
Immunogen Species:Homo sapiens ()
UniProt ID:P78363
Immunogen:Synthetic peptide of ABCA4
Raised in:Rabbit
Reactivity:
Tested Applications:ELISA, IHC; ELISA:1:2000-1:5000, IHC:1:50-1:200
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 molecµLes across extra- and intracellµLar 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 mµLticellµLar 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 molecµLe across the photoreceptor cell membrane. Mutations in this gene are found in patients diagnosed with Stargardt disease, a form of juvenile-onset macµLar degeneration. Mutations in this gene are also associated with retinitis pigmentosa-19, cone-rod dystrophy type 3, early-onset severe retinal dystrophy, fundus flavimacµLatus, and macµLar degeneration age-related 2.
Clonality:Polyclonal
Isotype:IgG
Purification Method:Antigen affinity purification
Conjµgate:Non-conjµgated
Buffer:-20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol
Form:Liquid
Stroage:Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Target Names:ABCA4
Research Areas:Neuroscience
Référence interne:
CSB-PA354357
URL de site web:
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