ACSF3 anticorps (C-Term)

N° du produit ABIN2785334

L’anticorps anti-ACSF3 Polyclonal produit chez le Lapin a été validé pour WB. Il convient pour la détection de ACSF3 dans des échantillons provenant de Humain, Souris, Cobaye, Rat, Boeuf (Vache), Chien, Cheval, Saccharomyces cerevisiae et Poisson zèbre (Danio rerio). }

Aperçu rapide pour ACSF3 anticorps (C-Term) (ABIN2785334)

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

Reactivité: Humain, Souris, Cobaye, Rat, 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)

Détail du produit anti-ACSF3 anticorps

Épitope: C-Term

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

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