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  2. Polyclonal

GTX47127

RHAG antibody, Internal

Cannot supply to this region.

SKU:
GTX47127
Additional Names:
Rh associated glycoprotein , CD241 , OHS , OHST , RH2 , RH50A , RHNR , Rh50 , Rh50GP , SLC42A1
Application:
WB
Concentration:
0.5-1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Protein A Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human
Buffer:
PBS, 2% Sucrose, 0.09% Sodium azide.
Immunogen:
A synthetic peptide corresponding to an Internal region of Human RHAG
Uniprot:
Q02094
Synonyms:
ammonium transporter Rh type A;CD241;erythrocyte membrane glycoprotein Rh50;erythrocyte plasma membrane 50 kDa glycoprotein;mutant Rh associated glycoprotein;OHS;OHST;Rh 50 glycoprotein;rh family type A glycoprotein;rh type A glycoprotein;RH2;Rh50;RH50A;Rh50GP;Rhesus associated polypeptide, 50-KD;rhesus blood group family type A glycoprotein;rhesus blood group-associated ammonia channel;Rhesus blood group-associated glycoprotein;RHNR;SLC42A1;truncated Rh-associated glycoprotein;truncated RhAG glycoprotein
Extra Details:
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]
Shipping Conditions:
Blue Ice