ACSF3 antibody (C-Term)

Catalog No. ABIN2785334

The Rabbit Polyclonal anti-ACSF3 antibody has been validated for WB. It is suitable to detect ACSF3 in samples from Human, Mouse, Rat, Guinea Pig, Cow, Dog, Horse, Saccharomyces cerevisiae and Zebrafish (Danio rerio).

Quick Overview for ACSF3 antibody (C-Term) (ABIN2785334)

Target: ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

Reactivity: Human, Mouse, Rat, Guinea Pig, Cow, Dog, Horse, Saccharomyces cerevisiae, Zebrafish (Danio rerio)

Host: Rabbit

Clonality: Polyclonal

Conjugate: This ACSF3 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-ACSF3 Antibody

Binding Specificity: C-Term

Sequence: YWNKPEETKS AFTLDGWFKT GDTVVFKDGQ YWIRGRTSVD IIKTGGYKVS

Predicted Reactivity: Cow: 93%, Dog: 93%, Guinea Pig: 100%, Horse: 93%, Human: 100%, Mouse: 100%, Rat: 100%, Yeast: 92%, Zebrafish: 93%

Characteristics: This is a rabbit polyclonal antibody against ACSF3. It was validated on Western Blot.

Purification: Affinity Purified

Immunogen: The immunogen is a synthetic peptide directed towards the C-terminal region of human ACSF3

Application Details

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Handling Advice: Avoid repeat freeze-thaw cycles.

Storage: -20 °C

Storage Comment: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Target Details for ACSF3

Target: ACSF3 (Acyl-CoA Synthetase Family Member 3 (ACSF3))

Alternative Name: ACSF3

Background: This gene encodes a member of the acyl-CoA synthetase family of enzymes that activate fatty acids by catalyzing the formation of a thioester linkage between fatty acids and coenzyme A. The encoded protein is localized to mitochondria, has high specificity for malonate and methylmalonate and possesses malonyl-CoA synthetase activity. Mutations in this gene are a cause of combined malonic and methylmalonic aciduria. Alternatively spliced transcript variants have been observed for this gene.
Protein Size: 311

Molecular Weight: 34 kDa

Gene ID: 197322

NCBI Accession: NM_001284316, NP_001271245

UniProt: F5H5A1