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Rabbit polyclonal ACAD9 antibody (A7798)
Supplier: ABclonal Inc.
Recommended applications: WB,IHC,IF
WB 1:500 – 1:2000 IHC 1:50 – 1:200 IF 1:50 – 1:100
Recommended protocols: check protocols
Click or hover above images to see image description for Rabbit polyclonal ACAD9 antibody.
Check alternative names for the antibodyExpand
Acyl CoA dehydrogenase 9 antibody|Acyl Coenzyme A dehydrogenase family, member 9 antibody|acyl-CoA dehydrogenase family member 9, mitochondrial antibody|FLJ23533 antibody|MGC14452 antibody|NPD002 antibody|Very long chain acyl CoA dehydrogenase VLCAD antibody|Anti-ACAD9 antibody (ab99952)
SCBT cat No: sc-135148|
Rabbit polyclonal ACAD9 antibody
|Catalogue No.|| |
Human, Mouse, Rat
Recombinant protein of human ACAD9
WB, IHC, IF
|Recommended dilution|| |
WB 1:500 – 1:2000
|Molecular weight|| |
Predicted: 69kDa/Observed: Refer to figures
ACAD9 antibody was tube-contained.
ACAD9 antibody was purified using affinity purification.
Store at -20 Celsius degree. Avoid freeze / thaw cycles.
|Alternative antibody names|| |
|Database links|| |
|Protein names|| |
|Protein function|| |
Required for mitochondrial complex I assembly . Has a dehydrogenase activity on palmitoyl-CoA (C16:0) and stearoyl-CoA (C18:0). It is three times more active on palmitoyl-CoA than on stearoyl-CoA. However, it does not play a primary role in long-chain fatty acid oxidation in vivo . Has little activity on octanoyl-CoA (C8:0), butyryl-CoA (C4:0) or isovaleryl-CoA (5:0).
|Protein tissue specificity|| |
Ubiquitously expressed in most normal human tissues and cancer cell lines with high level of expression in heart, skeletal muscles, brain, kidney and liver.
|Protein sequence and domain|| |
Belongs to the acyl-CoA dehydrogenase family.
|Protein cellular localization|| |
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.
AntibodyPlus can customize ACAD9 antibody according to your requirement, including bulk product size,etc. Please contact firstname.lastname@example.org. AntibodyPlus provides antibody trial sample for your own antibody validation.
|Product type|| |
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