Easy-Do PCR PreMix, 20ul reaction, 0.2ml thin-well tube
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Catalog number
EQ2.2-10X100
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Price
Please ask
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Size
10X100 vials
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Description
Easy-Do PCR PreMix, 20ul reaction, 0.2ml thin-well tube is a kit that is used to amplify a single copy or a several copies of a piece of DNA, generating many copies of an appropriate DNA sequence.
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Storage
Store at -20℃
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Shelf life
1 year
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Contents
U-Taq DNA Polymerase ; 10×PCR reaction buffer ; dNTPs (10 mM each) ; Loading dye ; Stabilizer
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Data sheet
Contact us to request a Data sheet
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Ordering
To order Easy-Do PCR PreMix, 20ul reaction, 0.2ml thin-well tube , please use the Cat. Nr.EQ2.2-10X100 and submit your purchase order by email or by fax. A discount is available for larger or bulk quantities, please contact us for more information
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Tips
Our specialists recommend you to follow carefully the pre-registered instructions for Easy-Do PCR PreMix, 20ul reaction, 0.2ml thin-well tube
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Group
PCR, polymerase chain reaction
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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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Additional description
Premixes for PCR contain dNTPs and MgCl. A PCR premix is much easier for DNA amplification than standard TAQ polymerase.
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Gene target
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Short name
Easy-Do PCR PreMix, 20ul , 2ml thin- tube
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Technique
Premix, 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. premix, SBS Genetcech tubes
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Alternative name
Easy-Do PCR test kit PreMix, 20ul reaction, 0.2ml thin-well tube
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Alternative technique
easyuse, tubes, dna-amplification
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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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