RHAG Polyclonal Antibody

Verified Samples in WB: 293T, K562, HepG2
Verified Samples in IHC: Human tonsil, Human cervical cancer

WB 1:1000-1:5000, IHC 1:50-1:300

Polyclonal

IgG

Fusion protein of human RHAG

RHAG

Abnormal Rhesus blood group associated glycoprotein, Ammonium transporter Rh type A, CD241, CD241 antigen, Erythrocyte membrane glycoprotein Rh50, Erythrocyte plasma membrane 50 kDa glycoprotein, Rh associated glycoprotein, Rh family type A glycoprotein, Rh type

Q02094

44 kDa

Refer to figures

Cell membrane, multi-pass membrane protein.

2.34 mg/mL

Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.

PBS with 0.05% NaN3 and 40% Glycerol, pH 7.4.

Antigen affinity purification

Cardiovascular

Unconjugated

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.