BCAT1 anticorps

N° du produit ABIN7236350

Détail du produit anti-BCAT1 anticorps

Antigène: BCAT1 (Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp BCAT1 est non-conjugé

Application: Immunohistochemistry (IHC), ELISA

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant protein of human BCAT1

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.4 mg/mL

Buffer: PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4

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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur BCAT1

Antigène: BCAT1 (Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))

Autre désignation: BCAT1 (BCAT1 Produits)

Synonymes: anticorps fj66g02, anticorps zgc:73157, anticorps wu:fj66g02, anticorps Bcatc, anticorps BCATC, anticorps BCT1, anticorps ECA39, anticorps MECA39, anticorps PNAS121, anticorps PP18, anticorps BCATc, anticorps Eca39, anticorps branched chain amino-acid transaminase 1, cytosolic, anticorps branched chain amino acid transaminase 1, anticorps branched chain amino-acid transaminase 1, cytosolic L homeolog, anticorps branched chain aminotransferase 1, cytosolic, anticorps bcat1, anticorps BCAT1, anticorps bcat1.L, anticorps Bcat1

Sujet: This gene encodes the cytosolic form of the enzyme branched-chain amino acid transaminase. This enzyme catalyzes the reversible transamination of branched-chain alpha-keto acids to branched-chain L-amino acids essential for cell growth. Two different clinical disorders have been attributed to a defect of branched-chain amino acid transamination: hypervalinemia and hyperleucine-isoleucinemia. As there is also a gene encoding a mitochondrial form of this enzyme, mutations in either gene may contribute to these disorders. Alternatively spliced transcript variants have been described.

NCBI Accession: NP_005495

UniProt: P54687