ACAD9 antibody (AA 92-621)

Catalog No. ABIN7877173

The Rabbit Polyclonal anti-ACAD9 antibody (ABIN7877173) specifically detects ACAD9 in ELISA, WB, IF, FACS and IHC (p). The antibody is reactive with Human samples.

Quick Overview for ACAD9 antibody (AA 92-621) (ABIN7877173)

Target: ACAD9 (Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ACAD9 antibody is un-conjugated

Application: ELISA, Western Blotting (WB), Immunofluorescence (IF), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Product Details anti-ACAD9 Antibody

Binding Specificity: AA 92-621

Purpose: Acyl-CoA dehydrogenase family member 9 Antibody / ACAD9

Purification: Antigen affinity purified

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.

Isotype: IgG

Application Details

Application Notes: Optimal dilution of the Acyl-CoA dehydrogenase family member 9 antibody should be determined by the researcher.

Restrictions: For Research Use only

Handling

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Storage: 4 °C,-20 °C

Storage Comment: 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.

Target Details for ACAD9

Target: ACAD9 (Acyl-CoA Dehydrogenase Family, Member 9 (ACAD9))

Alternative Name: Acyl-CoA dehydrogenase family member 9

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.

UniProt: Q9H845

Pathways: SARS-CoV-2 Protein Interactome