1_Drop PCR Mix [Squeeze Bottle. No Pipet]
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Descriptions
1_DROP PCR MIX [squeeze bottle. no pipet], the whole unit is disposable, 0,5ml size, 20+ PCR rxn, they prevent contamination between different samples, also air contamination, especially reliable, warm start, normal fidelity in order to perform the PCR.
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Application
Please consult labeling
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Shelf life
3months
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Sorage temperature
Store at -20 ℃
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Shipping condition
4°C
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Type of reagent
Please consult labeling
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Final product
Please consult labeling
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Regulatory approvals
Use only for research
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Tips
Our specialists recommend you to follow carefully the instructions when using the 1_Drop PCR Mix [Squeeze Bottle. No Pipet] . Check the lot number and expiration date before first use and follow the pre-written instructions in the technical sheet for long-term storage
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Ordering
To order 1_Drop PCR Mix [Squeeze Bottle. No Pipet], please use the Cat. N°.101Bio-W2599Sand 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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Technical file
Please contact our technical support - [email protected] - to request a datasheet, the user manual, certificate of analysis or the MSDS file.
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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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Gene target
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Short name
1_Drop PCR [Squeeze Bottle. No Pipet]
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Technique
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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Alternative name
1_Drop PCR test kit Mix [Squeeze Bottle. No liquid handling]
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Alternative technique
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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