Description
RHAG Polyclonal Antibody | E-AB-19025 | Gentaur US, UK & Europe Disrtribition
Reactivity: Human, Mouse
Host: Rabbit
Isotype: IgG
Application: WB, IHC, ELISA
Research Area: Cardiovascular
Background: The protein encoded by this gene is erythrocyte-specific and is thought to be part of a membrane channel that transports ammonium and carbon dioxide across the blood cell membrane. The encoded protein appears to interact with Rh blood group antigens and Rh30 polypeptides. Defects in this gene are a cause of regulator type Rh-null hemolytic anemia (RHN), or Rh-deficiency syndrome.RHAG (Rh-Associated Glycoprotein) is a Protein Coding gene. Diseases associated with RHAG include Anemia, Hemolytic, Rh-Null, Regulator Type and Stomatocytosis I. Among its related pathways are Transport of glucose and other sugars, bile salts and organic acids, metal ions and amine compounds and Erythrocytes take up carbon dioxide and release oxygen. GO annotations related to this gene include ankyrin binding and ammonium transmembrane transporter activity. An important paralog of this gene is RHCG.
Lead Time: 7~10 days
Concentration: 2.34 mg/mL
Storage: Store at -20°C. Avoid freeze / thaw cycles.
Immunogen: Fusion protein of human RHAG
Buffer: PBS with 0.05% NaN3 and 40% Glycerol, pH7.4
Purification: Antigen affinity purification
Dilution: WB 1:1000-1:5000, IHC 1:50-1:300, ELISA 1:5000-1:10000
Conjugation: Unconjugated
Calculated Molecular Weight: 44 kDa
Observed Molecular Weight: Refer to figures
Clonality: Polyclonal
