5’ and 3’ AAVS1 Positive Control Donor Vector Primer Mixes for Junction PCR Assays (10 µM)

  • Catalog number
    GE603PR-1
  • Price
    Please ask
  • Size
    100 ul
  • Shipping Temperature
    RT/Blue Ice/ Dry Ice
  • Product category
    Gene Editing
  • Description
    Isotype or positive controls by peptides, antibodies and deactivated samples. Positive controls are the same as the target vector or antibody or protein and can be spiked to the sample before the analysis starts.
  • Group
    PCR, polymerase chain reaction, positif
  • 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
    AAVS1   Donor   Vector   Primer   Mixes   for   Junction   Assays  
  • Gene symbol
    AAVS1, PPP1R12C
  • Short name
    5’ 3’ AAVS1 Positive Control Donor Vector Primer Mixes for Junction PCR Assays (10 µM)
  • Technique
    Positive, Control, PCR, controls, 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. Vectors
  • Alternative name
    5’ and 3’ AAVS1 Positive reference origin integrating Desoxyribonucleic acid sequence Primer Mixes to measure Junction PCR test kit tests (10 µM)
  • Alternative technique
    controls, pcr-sequence, dna-amplification
  • Tissue
    control, donor
Gene info
  • Identity
  • Gene
  • Long gene name
    adeno-associated virus integration site 1
  • Synonyms
  • GenBank acession
  • Locus
  • Discovery year
    1990-09-10
  • Entrez gene record
    17
  • Pubmed identfication
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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