RHAG antibody (AA 1-50)

Catalog No. ABIN6579575

This Rabbit Polyclonal antibody specifically detects RHAG in WB, IHC, ELISA and IF. It exhibits reactivity toward Human, Mouse and Rat.

Quick Overview for RHAG antibody (AA 1-50) (ABIN6579575)

Target: RHAG (Rh Family A Glycoprotein (RHAG))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This RHAG antibody is un-conjugated

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA, Immunofluorescence (IF)

Product Details anti-RHAG Antibody

Binding Specificity: AA 1-50

Purpose: CD241 Antibody

Specificity: CD241 Polyclonal Antibody detects endogenous levels of CD241 protein.

Purification: The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.

Immunogen: The antiserum was produced against synthesized peptide derived from the N-terminal region of human RHAG. AA range:1-50

Isotype: IgG

Application Details

Application Notes: WB 1:500 - 1:2000. IHC: 1:100-300 ELISA: 1:20000.. IF 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C/1 year

Expiry Date: 12 months

Target Details for RHAG

Target: RHAG (Rh Family A Glycoprotein (RHAG))

Alternative Name: RHAG

Background:

Synonyms: RHAG, RH50, Ammonium transporter Rh type A, Erythrocyte membrane glycoprotein Rh50, Erythrocyte plasma membrane 50 kDa glycoprotein, Rh50A, Rhesus blood group family type A glycoprotein, Rh family type A glycoprotein, Rh type A glycoprotein, Rhesus blood group-associated ammonia channel, Rhesus blood group-associated glycoprotein, CD241

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.[provided by RefSeq, Mar 2009],

Gene Name: RHAG

Protein Name: Ammonium transporter Rh type A

Molecular Weight: 44 kDa

Gene ID: 6005

OMIM: 180297

UniProt: Q02094