SPECIES REACTIVITY: | Human |
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TESTED APPLICATIONS: | ELISA, WB |
APPLICATIONS: | AADAC antibody can be used for detection of AADAC by ELISA at 1:1562500. AADAC antibody can be used for detection of AADAC by western blot at 2.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000. |
USER NOTE: | Optimal dilutions for each application to be determined by the researcher. |
POSITIVE CONTROL: | 1) Cat. No. XBL-10409 - Fetal Liver Tissue Lysate |
PREDICTED MOLECULAR WEIGHT: | 44 kDa |
IMMUNOGEN: | Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human AADAC. |
HOST SPECIES: | Rabbit |
PURIFICATION: | Antibody is purified by protein A chromatography method. |
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PHYSICAL STATE: | Lyophilized |
BUFFER: | Antibody is lyophilized in PBS buffer with 2% sucrose. Add 100 μL of distilled water. Final antibody concentration is 1 mg/mL. |
CONCENTRATION: | 1 mg/ml |
STORAGE CONDITIONS: | For short periods of storage (days) store at 4˚C. For longer periods of storage, store AADAC antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles. |
CLONALITY: | Polyclonal |
CONJUGATE: | Unconjugated |
ALTERNATE NAMES: | AADAC, DAC, CES5A1 |
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ACCESSION NO.: | NP_001077 |
PROTEIN GI NO.: | 68299767 |
OFFICIAL SYMBOL: | AADAC |
GENE ID: | 13 |
BACKGROUND: | Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens.Microsomal arylacetamide deacetylase competes against the activity of cytosolic arylamine N-acetyltransferase, which catalyzes one of the initial biotransformation pathways for arylamine and heterocyclic amine carcinogens. |
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REFERENCES: | 1) Frick, C., (2004) J. Biol. Chem. 279 (30), 31131-31138. |
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