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NSJ Bioreagents

SKU:RQ7607

Acyl-CoA dehydrogenase family member 9 Antibody / ACAD9

Acyl-CoA dehydrogenase family member 9 Antibody / ACAD9

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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.

Specifications

Family Primary antibody
Formulation 0.5mg/ml if reconstituted with 0.2ml sterile DI water
Format Antigen affinity purified
Host Animal Rabbit
Clonality Polyclonal (rabbit origin)
Isotype Rabbit IgG
Species Reactivity Human
Application WB, IHC-P, IF, FACS, Direct ELISA
Application Details Western blot: 0.5-1ug/ml,Immunohistochemistry (FFPE): 2-5ug/ml,IF,Flow cytometry: 1-3ug/million cells,Direct ELISA: 0.1-0.5ug/ml
Application Note Optimal dilution of the Acyl-CoA dehydrogenase family member 9 antibody should be determined by the researcher.
Localization Cytoplasmic (mitochondria)
Immunogen E. coli-derived recombinant human protein (amino acids K92-C621) was used as the immunogen for the Acyl-CoA dehydrogenase family member 9 antibody.
Buffer Lyophilized from 1X PBS with 2% Trehalose
Purity Antigen affinity purified
Storage After reconstitution, the Acyl-CoA dehydrogenase family member 9 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
Limitation This Acyl-CoA dehydrogenase family member 9 antibody is available for research use only.
Uniprot # Q9H845
Status Available
PDF Link https://www.nsjbio.com/tds-pdf/acyl-coa-dehydrogenase-family-member-9-antibody-acad9-rq7607
Title Acyl-CoA dehydrogenase family member 9 Antibody / ACAD9
Description 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.
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