FII Protrombin (G20210A) SNP-Screen RT-PCR test for detection of prothrombin F2 gene mutation (rs1799963), ready to use 0,2 ml tube format
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Catalog number
T01102-50-T
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Price
Please ask
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Size
60 tests
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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.
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Group
PCR, polymerase chain reaction, RT-PCR mixes
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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.
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Properties
Thermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
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Gene target
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Short name
FII Protrombin (G20210A) SNP-Screen RT-PCR test for of prothrombin F2 mutation (rs1799963), 2 tube format
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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
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Alternative name
FII Protrombin (G20210A) SNP-Screen Reverse transcription PCR test kit test to measure quantification on prothrombin coagulation factor II (thrombin) gene mutation (rs1799963), ready to use 0,2 milliliter tube supplied
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Alternative technique
rtpcrkits, tests, tubes, dna-amplification
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Alternative to gene target
coagulation factor II (thrombin), PT and RPRGL2 and THPH1, F2 and IDBG-42048 and ENSG00000180210 and 2147, thrombospondin receptor activity, Extracellular, F2 and IDBG-191373 and ENSMUSG00000027249 and 14061, F2 and IDBG-637247 and ENSBTAG00000007148 and 280685
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MeSH Data
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Name
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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.
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Tree numbers
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Qualifiers
ethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data
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