- Catalog number
- A05223-3
- Size / count
- 100 µg/Vial
- Dry ice
- No
- Hazardous
- No
- Discontinued
- No
- Background
- Acyl-CoA dehydrogenase family member 9, mitochondrial is an enzyme that in humans is encoded by the ACAD9 gene. This gene encodes a member of the acyl-CoA dehydrogenase family. Members of this family of proteins localize to the mitochondria and catalyze the rate-limiting step in the beta-oxidation of fatty acyl-CoA. The encoded protein is specifically active toward palmitoyl-CoA and long-chain unsaturated substrates. Mutations in this gene cause acyl-CoA dehydrogenase family member type 9 deficiency. Alternate splicing results in multiple transcript variants.
- Synonyms
- Histone deacetylase 10; HD10; HDAC10
- Gene Name
- ACAD9
- Gene ID
- 28976
- UniProt
- Q9H845
- Host
- Rabbit
- Reactivity
- Human
- Cross Reactivity
- No cross-reactivity with other proteins.
- Immunogen
- E.coli-derived human ACAD9 recombinant protein (Position: K92-C621) .
- Clonality
- Polyclonal
- Tissue Specificity
- Ubiquitous. High expression in liver, spleen, pancreas and kidney.
- Applications
- WB, IHC, IF, Flow Cytometry, ELISA
- Field of Research
- Acetylation, Chromatin Modifying Enzymes, Class I, Epigenetics and Nuclear Signaling, Signaling Pathways, Stem Cells
- Purification
- Immunogen affinity purified.
- Concentration
- Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
- Form
- Lyophilized
- Reconstitution
- Adding 0.2 ml of distilled water will yield a concentration of 500 μg/ml.
- Function
- Responsible for the deacetylation of lysine residues on the N-terminal part of the core histones (H2A, H2B, H3 and H4) . Histone deacetylation gives a tag for epigenetic repression and plays an important role in transcriptional regulation, cell cycle progression and developmental events. Histone deacetylases act via the formation of large multiprotein complexes.
- References & Citations
- 1. Dewulf, J. P., Barrea, C., Vincent, M.-F., De Laet, C., Van Coster, R., Seneca, S., Marie, S., Nassogne, M.-C. Evidence of a wide spectrum of cardiac involvement due to ACAD9 mutations: report on nine patients. Molec. Genet. Metab. 118: 185-189, 2016. 2. Ensenauer, R., He, M., Willard, J.-M., Goetzman, E. S., Corydon, T. J., Vandahl, B. B., Mohsen, A.-W., Isaya, G., Vockley, J. Human acyl-CoA dehydrogenase-9 plays a novel role in the mitochondrial beta-oxidation of unsaturated fatty acids. J. Biol. Chem. 280: 32309-32316, 2005. 3. Haack, T. B., Danhauser, K., Haberberger, B., Hoser, J., Strecker, V., Boehm, D., Uziel, G., Lamantea, E., Invernizzi, F., Poulton, J., Rolinski, B., Iuso, A., Biskup, S., Schmidt, T., Mewes, H.-W., Wittig, I., Meitinger, T., Zeviani, M., Prokisch, H. Exome sequencing identifies ACAD9 mutations as a cause of complex I deficiency. Nature Genet. 42: 1131-1134, 2010.
- Storage Conditions
- At -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freezing and thawing.
- Calculated Molecular Weight
- 39411 MW
- Observed Molecular Weight
- 69 kDa
- Applications Notes
- 6
- Gene Name Synonym
- Histone deacetylase 10
- Subcellular Location
- Cytoplasm. Nucleus. Excluded from the nucleoli.
- Protein Name
- Long-chain-fatty-acid--CoA ligase 5
- Isotype
- Rabbit IgG
- Contents
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4.