Geobacillus thermodenitrificans Heptaprenylglyceryl phosphate synthase (pcrB) -Baculovirus

• Catalog number
  GEN1142152.Baculovirus
• Price
  Please ask
• Size
  100ug

• Long name
  Recombinant Geobacillus thermodenitrificans 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
  GTNG_0254; pcrB; HepGP synthase
• General description
  Heptaprenylglyceryl phosphate synthase (pcrB) is a recombinant protein expressed in Baculovirus . 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
  Baculovirus
• 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.

• Gene target
  Geobacillus   thermodenitrificans   Heptaprenylglyceryl   phosphate   synthase   pcrB   Baculovirus  
• Short name
  Heptaprenylglyceryl phosphate synthase (pcrB)
• Alternative name
  Geobacillus thermodenitrificans Heptaprenylglyceryl phosphate synthase (pcrB) -Baculovirus

MeSH Data

• Name
  Polymerase Chain Reaction
• 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

Similar products