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ADA rabbit pAb
This gene encodes an enzyme that catalyzes the hydrolysis of adenosine to inosine. Various mutations have been described for this gene and have been linked to human diseases. Deficiency in this enzyme causes a form of severe combined immunodeficiency disease (SCID), in which there is dysfunction of both B and T lymphocytes with impaired cellular immunity and decreased production of immunoglobulins, whereas elevated levels of this enzyme have been associated with congenital hemolytic anemia. [provided by RefSeq, Jul 2008],
100
P00813
Cell membrane ; Peripheral membrane protein; Extracellular side. Cell junction. Cytoplasmic vesicle lumen. Cytoplasm. Lysosome. Colocalized with DPP4 at the cell surface..
Rabbit
Human,Rat,Mouse,
Synthesized peptide derived from human protein . at AA range: 80-160
Polyclonal
WB,ELISA
1 year
1 mg/mL
WB 1:500-2000 ELISA 1:5000-20000
39kD
PBS with 0.02% sodium azide and 50% glycerol pH 7.4. Store at -20°C. Avoid repeated freeze-thaw cycles.
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