ADA Polyclonal Antibody
Product Specifications
Background
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.
Synonyms
ADA
Gene ID
100
Swiss Prot
P00813
Cellular Locus
Cytoplasm, Cell membrane, Extracellular domain
Host
Rabbit
Cross Reactivity
Human, Mouse, Rat
Target
ADA
Clonality
Polyclonal
Isotype
IgG
Conjugation
Unconjugated
Source
Recombinant fusion protein containing a sequence corresponding to amino acids 1-363 of human ADA (NP_000013.2) .
Applications
WB, IF
Purification
Purified by Protein A.
Concentration
1µg/µl
Dilution
WB (1:300-5000), IF ()
Buffer
0.01M TBS (pH7.4) with 1% BSA, 0.02% Proclin300 and 50% Glycerol.
Modification
Unmodified
Storage Conditions
Store at -20°C for 12 months.
Gene ID URL
100
Frequently Asked Questions
More Discoveries
Explore Other Products
Browse additional items from our catalog
