2×TransTaq GENTAUR-T PCR SuperMix ( +dye)

  • Catalog number
    AS122-11
  • Price
    Please ask
  • Size
    1 ml
  • Group
    PCR, polymerase chain reaction
  • About
    TAQ or Pfu or Pfx or other enzymes are used for polycmerase chain reaction and have different specificity. The mores specific the lower the yield.
  • Properties
    Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
  • Gene target
  • Gene symbol
    TBXT, PLS3, ABAT, DBET, TBX21, H2BC20P, ARHGAP11B, RBMXL2, HLA-T, PRSS55
  • Short name
    2×TransTaq GENTAUR-T PCR SuperMix ( +dye)
  • Technique
    PCR, The polymerase chain reaction (PCR) amplifies the DNA in your sample. For real time PCR the cycle threshold Ct values willneed to be set before the experiment. Than the RT-PCR starts from RNA and real time PCR quantitates the cDNA so the RNA in the sample on given time of the experiment.
  • Label
    dye
  • Alternative name
    2×TransTaq GENTAUR-T PCR test kit SuperMix ( +dye)
  • Alternative technique
    dna-amplification
Gene info
  • Identity
  • Gene
  • Long gene name
    T-box transcription factor T
  • Synonyms gene
  • Synonyms gene name
    • T, brachyury homolog (mouse)
    • T brachyury transcription factor
  • GenBank acession
  • Locus
  • Discovery year
    1996-04-12
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • T-box transcription factors
  • VEGA ID
Gene info
Gene info
Gene info
Gene info
Gene info
  • Identity
  • Gene
  • Long gene name
    H2B clustered histone 20, pseudogene
  • Synonyms gene
  • Synonyms gene name
    • histone 2, H2bc
    • histone cluster 2, H2bc
    • histone cluster 2, H2bc (pseudogene)
    • histone cluster 2 H2B family member c (pseudogene)
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    2003-02-20
  • Entrez gene record
  • Pubmed identfication
  • RefSeq identity
  • Classification
    • H2B histones
  • VEGA ID
Gene info
Gene info
Gene info
Gene info
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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