Anti-Human/Mouse/Rat ADA Polyclonal Antibody

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.
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Properties

Data Sheet Click for Datasheet
Catalog Number PA12905
Size 100μl
Host Type Rabbit
Immunogen Recombinant protein of human ADA
Specificity Found in all tissues, occurs in large amounts in T-lymphocytes and, at the time of weaning, in gastrointestinal tissues.
Isotype IgG
Reacitivity Human,Mouse,Rat
Clone
Uniprot P00813
Concentration 0.1 mg/mL
Dilution WB 1:200-1:1000, IHC 1:25-1:100
Formulation
Application WB,IHC,ELISA
Other Names ada,ADA,ADA1,Adenosine aminohydrolase,Adenosine deaminase
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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