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You are here:Home » Antibodies » Abs to Disease Markers » Anti -ADA, CT (ADA1, Adenosine deaminase, Adenosine aminohydrolase) (PE)

Anti -ADA, CT (ADA1, Adenosine deaminase, Adenosine aminohydrolase) (PE)

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Specifications

Clone Host Grade Applications
Monoclonal Mouse Affinity Purified B
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.
Catalog #030746-PE
ApplicationsSuitable for use in Western Blot, FLISA.
Recommended DilutionFLISA: 1:1,000
Western Blot: 1:100~250
Storage and StabilityMay be stored at 4°C for short-term only. For long-term storage, store . Aliquots are stable for at least 6 months. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer. Do not freeze R-Phycoerythrin conjugates. Light sensitive.
Note Applications are based on unconjugated antibody.
Clone TypeMonoclonal
IsotypeIgG1
Clone No608CT2.1.3
HostMouse
SourceHuman
ConcentrationAs reported
FormSupplied as a liquid in PBS, pH 7.2. Contains ~0.09% sodium azide. Conjugated to R-Phycoerythrin (R-PE).
PurityPurified by Protein G affinity chromatography.
ImmunogenADA Mab is generated from mouses immunized with a KLH conjugated synthetic peptide selected from human ADA.
SpecificityHuman
Important NoteThis product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications without the expressed written authorization of United States Biological.
Alternate namesADA, ADA1, Adenosine deaminase, Adenosine aminohydrolase


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