MLYCD anticorps

N° du produit ABIN2856728

Détail du produit anti-MLYCD anticorps

Antigène: MLYCD (Malonyl CoA Decarboxylase (MLYCD))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MLYCD est non-conjugé

Application: Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris

Attributs du produit: Rabbit Polyclonal antibody to MCD (malonyl-CoA decarboxylase)
MCD antibody [N2C1], Internal

Purification: Purified by antigen-affinity chromatography.

Immunogène: Recombinant protein encompassing a sequence within the center region of human MCD. The exact sequence is proprietary.

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Commentaires:

Positive Control: C8D30

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1XPBS ( pH 7), 20 % Glycerol, 0.01 % Thimerosal

Agent conservateur: Thimerosal (Merthiolate)

Précaution d'utilisation: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: 4 °C,-20 °C

Stockage commentaire: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Détails sur MLYCD

Antigène: MLYCD (Malonyl CoA Decarboxylase (MLYCD))

Autre désignation: malonyl-CoA decarboxylase (MLYCD Produits)

Synonymes: anticorps MCD, anticorps AI324784, anticorps Mcd, anticorps MaLonyl CoA Decarboxylase, anticorps malonyl-CoA decarboxylase, anticorps mlcd-1, anticorps MLYCD, anticorps Mlycd

Sujet: The product of this gene catalyzes the breakdown of malonyl-CoA to acetyl-CoA and carbon dioxide. Malonyl-CoA is an intermediate in fatty acid biosynthesis, and also inhibits the transport of fatty acyl CoAs into mitochondria. Consequently, the encoded protein acts to increase the rate of fatty acid oxidation. It is found in mitochondria, peroxisomes, and the cytoplasm. Mutations in this gene result in malonyl-CoA decarboyxlase deficiency.

Cellular Localization: Mitochondrion , Cytoplasm , Peroxisome

Poids moléculaire: 55 kDa

ID gène: 23417

UniProt: O95822

Pathways: Regulation of Carbohydrate Metabolic Process