BCAT1 Protein (Myc-DYKDDDDK Tag)

Produktnummer ABIN2715183

Produktdetails

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

Protein-Typ: Recombinant

Spezies: Human

Quelle: HEK-293 Cells

Aufreinigungstag / Konjugat: Dieses BCAT1 Protein ist gelabelt mit Myc-DYKDDDDK Tag.

Applikation: Antibody Production (AbP), Standard (STD)

Produktmerkmale:

• Recombinant human BCAT1 protein expressed in HEK293 cells.
• Produced with end-sequenced ORF clone

Reinheit: > 80 % as determined by SDS-PAGE and Coomassie blue staining

Anwendungsinformationen

Applikationshinweise: Recombinant human proteins can be used for:
Native antigens for optimized antibody production
Positive controls in ELISA and other antibody assays

Kommentare:

The tag is located at the C-terminal.

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Konzentration: 50 μg/mL

Buffer: 25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10 % glycerol.

Lagerung: -80 °C

Informationen zur Lagerung: 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.

Antigendetails

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

Andere Bezeichnung: Bcat1 (BCAT1 Produkte)

Synonyme: 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

Hintergrund: 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.

Molekulargewicht: 42.8 kDa

NCBI Accession: NP_005495