Anti-SLC4A1 aptamer SELEX Service(Cat#: CTApt-1845)
This is an aptamer development services to screening aptamers binds to the SLC4A1 with an affinity of 1nM~1μM.
Specific Inquiry 
Summary
Specifications
| Target Category |
Protein |
| Target |
SLC4A1 |
| Alternative Names |
Solute Carrier Family 4 Member 1 (Diego Blood Group) ; Solute Carrier Family 4, Anion Exchanger, Member 1 (Erythrocyte Membrane Protein Band 3, Diego Blood Group) ; Solute Carrier Family 4 (Anion Exchanger), Member 1 (Diego Blood Group) ; Erythrocyte Membrane Protein Band 3; Band 3 Anion Transport Protein; Anion Exchange Protein 1; Waldner Blood Group; Froese Blood Group; Wright Blood Group; Swann Blood Group; Diego Blood Group; CD233; RTA1A; EPB3; Solute Carrier Family 4 (Anion Exchanger), Member ; Solute Carrier Family 4, Anion Exchanger, Number 1; Erythroid Anion Exchange Protein; Solute Carrier Family 4 Member 1; Band 3 Anion Exchanger; Anion Exchanger-1; Anion Exchanger 1; CD233 Antigen; SLC4A1; EMPB3; BND3; SPH4; AE 1; CHC; WD1 |
| Gene ID |
6521 |
| UniProt ID |
P02730 |
| Target Overview |
The protein encoded by this gene is part of the anion exchanger (AE) family and is expressed in the erythrocyte plasma membrane, where it functions as a chloride/bicarbonate exchanger involved in carbon dioxide transport from tissues to lungs. The protein comprises two domains that are structurally and functionally distinct. The N-terminal 40kDa domain is located in the cytoplasm and acts as an attachment site for the red cell skeleton by binding ankyrin. The glycosylated C-terminal membrane-associated domain contains 12-14 membrane spanning segments and carries out the stilbene disulphonate-sensitive exchange transport of anions. The cytoplasmic tail at the extreme C-terminus of the membrane domain binds carbonic anhydrase II. The encoded protein associates with the red cell membrane protein glycophorin A and this association promotes the correct folding and translocation of the exchanger. This protein is predominantly dimeric but forms tetramers in the presence of ankyrin. Many mutations in this gene are known in man, and these mutations can lead to two types of disease: destabilization of red cell membrane leading to hereditary spherocytosis, and defective kidney acid secretion leading to distal renal tubular acidosis. Other mutations that do not give rise to disease result in novel blood group antigens, which form the Diego blood group system. Southeast Asian ovalocytosis (SAO, Melanesian ovalocytosis) results from the heterozygous presence of a deletion in the encoded protein and is common in areas where Plasmodium falciparum malaria is endemic. One null mutation in this gene is known, resulting in very severe anemia and nephrocalcinosis. |
| Chemical Modification |
N/A |
| Type |
DNA |
| Length |
20-80 nt |
| Affinity (Kd) |
1nM~1μM |
| Binding Conditions/Buffer |
PBS; buffer system with Serum; other |
For Research Use Only. Not for Diagnostic or Therapeutic Applications.
