Rabbit ACAD9 Polyclonal Antibody | anti-ACAD9 antibody

ACAD9 Rabbit Polyclonal

Cat. Num. AAA766294

• Gene Names: ACAD9; NPD002
• Reactivity: Human, Mouse, Rat
• Applications: ELISA, Western Blot, Immunohistochemistry
• Purity: >=95% as determined by SDS-PAGE; Immunogen Affinity Purified
• Synonyms: ACAD9; Polyclonal Antibody; ACAD9 Rabbit Polyclonal; anti-ACAD9 antibody

• Host: Rabbit
• Reactivity: Human, Mouse, Rat
• Clonality: Polyclonal
• Isotype: IgG
• Purity/Purification: >=95% as determined by SDS-PAGE; Immunogen Affinity Purified
• Form/Format: Liquid
• Sequence Length: 621

• Applicable Applications for anti-ACAD9 antibody: ELISA (EIA), Western Blot (WB), Immunohistochemistry (IHC)
• Immunogen: Acyl-Coenzyme A dehydrogenase family, member 9
• Preparation and Storage: PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20 degree C for 24 months (Avoid repeated freeze / thaw cycles.)

Immunohistochemistry (IHC)

(Immunohistochemistry of paraffin-embedded human colon cancer using MBS766294 (ACAD9 antibody) at dilution of 1:50)

Western Blot (WB)

(MCF7 cells were subjected to SDS PAGE followed by western blot with MBS766294 (ACAD9 antibody) at dilution of 1:500)

NCBI and Uniprot Product Information

• NCBI GI #: 21361497
• NCBI GeneID: 28976
• NCBI Accession #: NP_054768.2
• NCBI GenBank Nucleotide #: NM_014049.4
• Molecular Weight: 68,760 Da
• NCBI Official Full Name: acyl-CoA dehydrogenase family member 9, mitochondrial
• NCBI Official Synonym Full Names: acyl-CoA dehydrogenase family member 9
• NCBI Official Symbol: ACAD9
• NCBI Official Synonym Symbols: NPD002
• NCBI Protein Information: acyl-CoA dehydrogenase family member 9, mitochondrial
• UniProt Protein Name: Acyl-CoA dehydrogenase family member 9, mitochondrial
• Protein Family: Acyl-CoA dehydrogenase family
• UniProt Gene Name: ACAD9
• UniProt Synonym Gene Names: ACAD-9
• UniProt Entry Name: ACAD9_HUMAN

NCBI Description

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.[provided by RefSeq, Mar 2010]

Uniprot Description

ACAD9: Has a dehydrogenase activity on palmitoyl-CoA (C16:0) and stearoyl-CoA (C18:0). It is three times more active on palmitoyl-CoA then on stearoyl-CoA. Has little activity on octanoyl-CoA (C8:0), butyryl-CoA (C4:0) or isovaleryl-CoA (5:0). Belongs to the acyl-CoA dehydrogenase family.

Protein type: Oxidoreductase; EC 1.3.99.-; Mitochondrial

Chromosomal Location of Human Ortholog: 3q21.3

Cellular Component: dendrite; mitochondrial inner membrane; mitochondrion; nucleus

Molecular Function: acyl-CoA binding; acyl-CoA dehydrogenase activity; electron carrier activity; FAD binding; protein binding

Biological Process: fatty acid beta-oxidation using acyl-CoA dehydrogenase; lipid homeostasis; mitochondrial respiratory chain complex I assembly

Disease: Acyl-coa Dehydrogenase Family, Member 9, Deficiency Of