ACAD9 Antibody

Product Specifications

Background

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.

NCBI Gene ID

28976

Swiss Prot

Q9H845

Host

Rabbit

Reactivity

Human, Mouse

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 1-270 of human ACAD9 (NP_054768.2) .

Clonality

Polyclonal

Conjugation

Unconjugated

Type

Primary Antibodies

Field of Research

Cancer, Signal Transduction

Purification

Affinity purification

Positive Control

SKOV3

Concentration

Batch dependent

Buffer

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

Modification

None

Shipping Conditions

Blue Ice

Storage Conditions

Store at -20˚ C. Avoid freeze / thaw cycles.

Calculated Molecular Weight

Observed: 69kDa

Fragment

IgG

Symbol

ACAD9

Positive Control 2

U-251MG

Positive Control 3

MCF7

Positive Control 4

293T

Positive Control 5

NCI-H460

Positive Control 6

Mouse kidney

NCBI Official Name

Acyl-CoA dehydrogenase family member 9

NCBI Organism

Homo sapiens

Other Product Names

MC1DN2NPD002, acyl-CoA dehydrogenase family member 9, mitochondrial, acyl-Coenzyme A dehydrogenase family, member 9, very-long-chain acyl-CoA dehydrogenase VLCAD