MTR (A2756G) SNP-Screen RT-PCR test for detection of methionine synthase gene mutation (Asp919Gly; rs1805087), ready to use 0,2 ml tube format

  • Catalog number
    T01143-50-T
  • Price
    Please ask
  • Size
    60 tests
  • Description
    The detections of the targets with this kit is a type of test that can be performed on any target containing biological samples after clean up of interfering agents. The assay must be performed following the protocol. cDNA genes are a locus (or region) of DNA for functional transcript RNA or protein. An ELISA is used to detect the expressed protein in biological fluids, serum, saliva.
  • Group
    PCR, polymerase chain reaction, RT-PCR mixes
  • 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
    MTR
  • Short name
    MTR (A2756G) SNP-Screen RT-PCR test for of methionine synthase mutation (Asp919Gly; rs1805087), 2 tube format
  • Technique
    detection, RT-PCR, tube, 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. Sacace tubes
  • Alternative name
    MTR (A2756G) SNP-Screen Reverse transcription PCR test kit test to measure quantification on methionine synthase gene mutation (Asp919Gly; rs1805087), ready to use 0,2 milliliter tube supplied
  • Alternative technique
    rtpcrkits, tests, tubes, dna-amplification
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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