ACSF3 anticorps (C-Term)

N° du produit ABIN2785334

Détail du produit anti-ACSF3 anticorps

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

Épitope: C-Term

Reactivité: Humain, Souris, Rat, Cobaye, Boeuf (Vache), Chien, Cheval, Saccharomyces cerevisiae, Poisson zèbre (Danio rerio)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ACSF3 est non-conjugé

Application: Western Blotting (WB)

Séquence: YWNKPEETKS AFTLDGWFKT GDTVVFKDGQ YWIRGRTSVD IIKTGGYKVS

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

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

Purification: Affinity Purified

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

Information d'application

Restrictions: For Research Use only

Stockage

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.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeat freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: 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.

Détails sur ACSF3

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

Autre désignation: ACSF3 (ACSF3 Produits)

Synonymes: anticorps BB101783, anticorps acyl-CoA synthetase family member 3, anticorps ACSF3, anticorps Acsf3

Sujet: 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

Poids moléculaire: 34 kDa

ID gène: 197322

NCBI Accession: NM_001284316, NP_001271245

UniProt: F5H5A1