BCAT1 Protein (Myc-DYKDDDDK Tag)
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- Antigène Voir toutes BCAT1 Protéines
- BCAT1 (Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
- Type de proteíne
- Recombinant
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Origine
- Humain
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Source
- HEK-293 Cells
- Purification/Conjugué
- Cette BCAT1 protéine est marqué à la Myc-DYKDDDDK Tag.
- Application
- Antibody Production (AbP), Standard (STD)
- Attributs du produit
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- Recombinant human BCAT1 protein expressed in HEK293 cells.
- Produced with end-sequenced ORF clone
- Pureté
- > 80 % as determined by SDS-PAGE and Coomassie blue staining
- Top Product
- Discover our top product BCAT1 Protéine
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- Indications d'application
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Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays - Commentaires
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The tag is located at the C-terminal.
- Restrictions
- For Research Use only
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- Concentration
- 50 μg/mL
- Buffer
- 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.
- Stock
- -80 °C
- Stockage commentaire
- Store at -80°C. Thaw on ice, aliquot to individual single-use tubes, and then re-freeze immediately. Only 2-3 freeze thaw cycles are recommended.
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- Antigène
- BCAT1 (Branched Chain Amino-Acid Transaminase 1, Cytosolic (BCAT1))
- Autre désignation
- Bcat1 (BCAT1 Produits)
- Synonymes
- fj66g02 Protein, zgc:73157 Protein, wu:fj66g02 Protein, Bcatc Protein, BCATC Protein, BCT1 Protein, ECA39 Protein, MECA39 Protein, PNAS121 Protein, PP18 Protein, BCATc Protein, Eca39 Protein, branched chain amino-acid transaminase 1, cytosolic Protein, branched chain amino acid transaminase 1 Protein, branched chain amino-acid transaminase 1, cytosolic L homeolog Protein, branched chain aminotransferase 1, cytosolic Protein, bcat1 Protein, BCAT1 Protein, bcat1.L Protein, Bcat1 Protein
- 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.
- Poids moléculaire
- 42.8 kDa
- NCBI Accession
- NP_005495
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