ACADL Antibody Cat. No.: 25-166

ACADL Antibody

Specifications

HOST SPECIES: Rabbit

SPECIES REACTIVITY: Human, Mouse

Antibody produced in rabbits immunized with a synthetic peptide corresponding a region IMMUNOGEN: of human ACADL.

TESTED APPLICATIONS: ELISA, WB

ACADL antibody can be used for detection of ACADL by ELISA at 1:312500. ACADL APPLICATIONS: antibody can be used for detection of ACADL by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

POSITIVE CONTROL: 1) Cat. No. 1309 - Human Placenta Lysate

PREDICTED MOLECULAR 44 kDa WEIGHT:

Properties

PURIFICATION: Antibody is purified by peptide affinity chromatography method.

CLONALITY: Polyclonal

CONJUGATE: Unconjugated

PHYSICAL STATE: Liquid

September 26, 2021 1 https://www.prosci-inc.com/acadl-antibody-25-166.html Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% BUFFER: sucrose.

CONCENTRATION: batch dependent

For short periods of storage (days) store at 4˚C. For longer periods of storage, store STORAGE CONDITIONS: ACADL antibody at -20˚C. As with any antibody avoid repeat freeze-thaw cycles.

Additional Info

OFFICIAL SYMBOL: ACADL

ALTERNATE NAMES: ACADL, ACAD4, LCAD

ACCESSION NO.: NP_001599

PROTEIN GI NO.: 4501857

GENE ID: 33

USER NOTE: Optimal dilutions for each application to be determined by the researcher.

Background and References

ACADL belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta- oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl- CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.The protein BACKGROUND: encoded by this gene belongs to the acyl-CoA dehydrogenase family, which is a family of mitochondrial flavoenzymes involved in fatty acid and branched chain amino-acid metabolism. This protein is one of the four enzymes that catalyze the initial step of mitochondrial beta-oxidation of straight-chain fatty acid. Defects in this gene are the cause of long-chain acyl-CoA dehydrogenase (LCAD) deficiency, leading to nonketotic hypoglycemia.

REFERENCES: 1) Lea, W., Biochim. Biophys. Acta 1485 (2-3), 121-128 (2000).

ANTIBODIES FOR RESEARCH USE ONLY.

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