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BCAT1 anticorps
BCAT1
Reactivité: Humain, Souris
IHC, ELISA
Hôte: Lapin
Polyclonal
unconjugated
N° du produit ABIN7236350
Détail du produit anti-BCAT1 anticorps
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Antigène
Voir toutes BCAT1 Anticorps
BCAT1
(Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
Reactivité
Toutes les réactivités sur BCAT1 Anticorps
Humain, Souris
Hôte
Toutes les hôtes sur BCAT1 Anticorps
Lapin
Clonalité
Toutes les clonalités sur BCAT1 Anticorps
Polyclonal
Conjugué
Tous les conjugués à travers BCAT1 Anticorps
Cet anticorp BCAT1 est non-conjugé
Application
Tous les applications à travers BCAT1 Anticorps.
Immunohistochemistry (IHC), ELISA
Attributs du produit
Polyclonal Antibody
Purification
Affinity purification
Immunogène
Recombinant protein of human BCAT1
Isotype
IgG
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Alternatives
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Information d'application
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Indications d'application
IHC 1:50-1:200
Restrictions
For Research Use only
Stockage
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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
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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
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