Bacillus thuringiensis Heptaprenylglyceryl phosphate synthase (pcrB) -Mammalian Cell

  • Catalog number
    GEN1005575.Mammalian Cell
  • Price
    Please ask
  • Size
    100ug
  • Long name
    Recombinant Bacillus thuringiensis Heptaprenylglyceryl phosphate synthase (pcrB)
  • Alternative names
    geranylgeranylglyceryl phosphate synthase; Heptaprenylglyceryl phosphate synthase; geranylgeranylglyceryl phosphate synthase; Glycerol-1-phosphate heptaprenyltransferase
  • Gene name
    pcrB
  • Other gene names
    BALH_0296; pcrB; HepGP synthase
  • General description
    Heptaprenylglyceryl phosphate synthase(pcrB) is a recombinant protein expressed in Mammalian Cell . The protein can be with or without a His-Tag or other tag in accordance to customer's request. All of our recombinant proteins are manufactured in strictly controlled facilities and by using a well established technology which guarantees full batch-to-bact consistency and experiment reproducibility.
  • Product category
    Recombinant Proteins
  • Expression system
    Mammalian Cell
  • Available also expressed in
    E Coli ; Yeast ; Baculovirus ; Mammalian Cell
  • Purity
    Greater than 90% (determined by SDS-PAGE)
  • Form
    Lyophilized protein
  • Storage
    This protein can be stored at -20 degrees Celsius. For extended periods of time it is recommended to keep the protein frozen at -40 or -80 degrees Celsius. Avoid cycles of freezing and thawing as they might denaturate the polypeptide chains.
  • Applications
    This protein can be used as a positive control for applications such as ELISA, IFA, RIA, Western Blot, etc.
  • Description
    Bacillus Anthracis and Cereus are the most known Bacilli. Anthrax has a very high toxin level and is used in Biologic warfare. However 1 is a harmless product. For cells, cell lines and tissues in culture till half confluency.
MeSH Data
  • Name
  • Concept
    Scope note: In vitro method for producing large amounts of specific DNA or RNA fragments of defined length and sequence from small amounts of short oligonucleotide flanking sequences (primers). The essential steps include thermal denaturation of the double-stranded target molecules, annealing of the primers to their complementary sequences, and extension of the annealed primers by enzymatic synthesis with DNA polymerase. The reaction is efficient, specific, and extremely sensitive. Uses for the reaction include disease diagnosis, detection of difficult-to-isolate pathogens, mutation analysis, genetic testing, DNA sequencing, and analyzing evolutionary relationships.
  • Tree numbers
    • E05.393.620.500
  • Qualifiers
    ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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