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Last updated: 2017/4/23

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BCAT1 rabbit monoclonal antibody

  • Catalog # : H00000586-K
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  • Specification
  • Product Description:
  • Rabbit monoclonal antibody raised against a human BCAT1 peptide using ARM Technology.
  • Immunogen:
  • A synthetic peptide of human BCAT1 is used for rabbit immunization.
    Customer or Abnova will decide on the preferred peptide sequence.
  • Host:
  • Rabbit
  • Reactivity:
  • Human
  • Purification:
  • Protein A
  • Isotype:
  • IgG
  • Quality Control Testing:
  • Antibody reactive against human BCAT1 peptide by ELISA and mammalian transfected lysate by Western Blot.
  • Storage Buffer:
  • In 1x PBS, pH 7.4
  • Storage Instruction:
  • Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
  • Note:
  • 1. Customer may provide cell or tissue lysate for antibody screening.
    2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.
  • Library Construction:
  • Non-fusion antibody library from rabbit spleen (ARM Technology).
  • Expression:
  • Overexpression vector and transfection into 293H cell line.
  • Deliverable:
  • Up to three rabbit IgG clones of 1 mg each will be delivered to customer.
  • Applications
  • ELISA
  • Application Image
  • Western Blot (Transfected lysate)
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 586
  • GeneBank Accession#:
  • BCAT1
  • Gene Name:
  • BCAT1
  • Gene Alias:
  • BCT1,DKFZp686E12175,ECA39,MECA39,PNAS-121,PP18
  • Gene Description:
  • branched chain aminotransferase 1, cytosolic
  • Gene Summary:
  • 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
  • Other Designations:
  • branched-chain-amino-acid aminotransferase, cytosolic,placental protein 18
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