BCAT1 Antibody

Western Blot: BCAT1 Antibody [H00000586-B01P] - Analysis of BCAT1 expression in transfected 293T cell line by BCAT1 polyclonal antibody. Lane 1: BCAT1 transfected lysate(35.31 KDa). Lane 2: Non-transfected lysate.

Product Discontinued

BCAT1 Antibody Summary

• Description: Quality control test: Antibody reactive against mammalian transfected lysate.
• Immunogen: BCAT1 (AAH33864, 1 a.a. - 320 a.a.) full-length human protein. MDCSNGCSAECTGEGGSKEVVGTFKAKDLIVTPATILKEKPDPNNLVFGTVFTDHMLTVEWSSEFGWEKPHIKPLQNLSLHPGSSALHYAVELFEGLKAFRGVDNKIRLFQPNLNMDRMYRSAVRATLPVFDKEELLECIQQLVKLDQEWVPYSTSASLYIRPTFIGTEPSLGVKKPTKALLFVLLSPVGPYFSSGTFNPVSLWANPKYVRAWKGGTGDCKMGGNYGSSLFAQCEAVDNGCQQVLWLYGEDHQITEVGTMNLFLYWINEDGEEELATPPLDGIILPGVTRRCILDLAHQWDTELSLFSINLPDFLQFIYF
• Specificity: BCAT1 - branched chain aminotransferase 1, cytosolic,
• Isotype: IgG
• Clonality: Polyclonal
• Host: Mouse
• Gene: BCAT1
• Purity: Protein A purified

Applications/Dilutions

• Dilutions:
  • Western Blot
• Application Notes: Antibody reactivity against Recombinant Protein with GST tag on ELISA and WB and also on transfected lysate in WB. GST tag alone is used as a negative control.

Packaging, Storage & Formulations

• Storage: Aliquot and store at -20C or -80C. Avoid freeze-thaw cycles.
• Buffer: PBS (pH 7.4)
• Preservative: No Preservative
• Purity: Protein A purified

Notes

This product is produced by and distributed for Abnova, a company based in Taiwan.

Alternate Names for BCAT1 Antibody

• BCAT(c)
• BCAT1
• BCAT-1
• BCATC
• BCT1
• BCT1PNAS121
• branched chain amino-acid transaminase 1, cytosolic
• branched chain aminotransferase 1, cytosolic
• branched-chain-amino-acid aminotransferase, cytosolic
• DKFZp686E12175
• EC 2.6.1.42
• ECA39
• MECA39
• placental protein 18
• PNAS121
• PP18
• Protein ECA39

Background

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. [provided by RefSeq]

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

Bioinformatics

• Gene Symbol: BCAT1
• Entrez:
  • 586(Human)