epitope corresponding to amino acids 929-1144 of ABCC11 of human origin
Modification Notes
ATP-binding cassette (ABC) transporters belong to an evolutionarily conserved family of proteins that catalyze the transport of molecules across extra- and intracellular membranes through the energy of ATP hydrolysis. ABC genes comprise seven subfamilies, designated ABC1, MDR/TAP, MRP, ALD, OABP, GCN20 and White (1). The complete human ABCC subfamily has 12 identified members (ABCC1–12), nine from the multidrug resistance-like subgroup, two from the sulfonylurea receptor subgroup, and the CFTR gene (2). The human ABCC11 gene maps to chromosome 16q12.1 and encodes a 1,382 amino acid protein (1–4). The human ABCC12 gene maps to chromosome 16q12.1 and encodes a 1,359 amino acid protein (1,4). Transcripts of ABCC11 and ABCC12 genes are present in various adult human tissues, including liver, lung and kidney, and also in several fetal tissues (3,4). Their chromosomal localization, potential function and expression patterns identify them as candidates for paroxysmal kinesigenic choreoathetosis, a disorder characterized by attacks of involuntary movements and postures, chorea and dystonia (1,3). Other inherited disorders where ABC transporters are implicated include cystic fibrosis, neurological disease, retinal degeneration, cholesterol and bile transport defects, anemia and drug response (5,6).
Key Feature
Clonality
Polyclonal
Isotype
IgG
Host Species
Rabbit
Tested Applications
WBIPIFELISA
recommended for detection of ABCC11 of human origin by WB, IP, IF and ELISA:
Species Reactivity
HumanMouseRat
Concentration
1mg/ml
Purification
Affinity purified
Target Information
Alternative Names
epitope corresponding to amino acids 929-1144 of ABCC11 of human origin
Tissue Specificity
epitope corresponding to amino acids 929-1144 of ABCC11 of human origin