hsa-mir-663a RT-PCR Detection and U6 Calibration Kit
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Catalog numberabx096638
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Price:
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Size50 rxns
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CategoryPCR Kits
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ClonalityN/A
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Raised inN/A
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TargetPCR Detection and U6 Calibration
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Immunogensee included datasheet or contact us
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Species reactivityHuman, Mouse, Rat (for other species please inquire)
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PurificationAffinity purified
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ApplicationsWB (for other applications please contact us)
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Stock availabilityShipped within 5-10 working days.
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Storage conditionsAliquot and store at -20 °C. Avoid repeated freeze/thaw cycles.
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FootnoteThis product is for research use only.
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DescriptionThe 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.
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GroupPCR, polymerase chain reaction, RT-PCR mixes
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AboutTAQ 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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PropertiesThermocyclers can be callibrated for identical ramping curves to obtain a more accurate PCR.
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Gene target
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Short namehsa-mir-663a RT-PCR U6 Calibration Kit
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Techniquedetection, RT-PCR, 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.
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LabelNo Label
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Alternative namehsa-mir-663a Reverse transcription PCR test kit quantification and U6 Calibration reagent
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Alternative techniquertpcrkits, kits, dna-amplification
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Alternative to gene targetv-kit Hardy-Zuckerman 4 feline sarcoma viral oncogene homolog, C-Kit and CD117 and PBT and SCFR, KIT and IDBG-18980 and ENSG00000157404 and 3815, transferase activity, Extracellular, Kit and IDBG-172083 and ENSMUSG00000005672 and 16590, KIT and IDBG-642326 and ENSBTAG00000002699 and 280832
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MeSH Data
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Name
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ConceptScope 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
- E05.393.620.500
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Qualifiersethics, trends, veterinary, history, classification, economics, instrumentation, methods, standards, statistics & numerical data