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2X TOPsimple™ PreMIX (aliquot)–multi HOT

No Product Name Cat.# Conc Size Price(₩) Add
1 2X TOPsimple™ PreMIX (aliquot)–multi HOT P661HC 2X 96 tubes ₩ 90,000 추가
2 2X TOPsimple™ PreMIX (aliquot)–multi HOT P662HC 2X 960 tubes ₩ 720,000 추가
3 2X TOPsimple™ PreMIX (aliquot)–multi HOT P661HC-50 2X 96 tubes ₩ 180,000 추가
4 2X TOPsimple™ PreMIX (aliquot)–multi HOT P662HC-50 2X 960 tubes ₩ 1,440,000 추가
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Product description

2X TOPsimple™ PreMIX (aliquot)-multi HOT is aliquoted into PCR tube strips. For example, 8 strips of 12 tubes are provided for 96 PCR reactions (Cat. P661HC). 2X TOPsimple™ PreMIX-HOT is a ready-to-use PCR mixture containing 2X concentration of DNA polymerase, reaction buffer and dNTP. This product can be used in general multiplex PCR and genotyping experiment related to genetic diagnostics because it produces up to 20 different amplified products within a single tube reaction.

 

Characteristics

- Single-tube convenience

- Well-suited to analysis of a large number of samples.

- A-tail formation at 3’ ends of amplified duplex DNA

 

Applications

- High specific amplification of DNA fragments shorter than 3 kb.

- Amplification of cDNA and genomic DNA.

- Amplification of template DNA with secondary or higher ordered structure that is resistant to PCR amplification

- Primer extension

- Multiplex PCR

- Well-suited for an automated PCR machines, for which PCR reaction mixtures are prepared at the room 

  temperature

- Colony PCR

- Labeling of DNA fragments with radioactive-isotopes

- Nucleotide sequencing 

 

Components (2X)

- nTaq-multi HOT DNA polymerase: 0.2 unit/µl

- nTaq-multi HOT buffer (containing 4 mM MgCl2)

- dNTP mixture: 0.4 mM each

- Stabilizer

 

Storage

Stable up to 18 months at -20 or 3 months at 4 (Storage at -20 is recommended).

 

Standard reaction conditions

PCR mixturea

Component

Reaction volume

(20 μl)

Reaction volume

(50 μl)

2X TOPsimple™ PreMIX(aliquot)-multi HOT

1 tube

1 tube

Template DNAb (0.1~500 ng/μl)

1 μl

2.5 μl

Primer 1 (5 pmole/μl)

1 μl

2.5 μl

Primer 2 (5 pmole/μl)

1 μl

2.5 μl

Sterile water

up to 20 μl

up to 50 μl

aAssmeble the reaction mixture on ice

bPlasmid DNA, 0.1 ng-30 ng; genomic DNA, 50 ng-500 ng

 

- PCR cycles

Step

Temperature

Time

Cycle

Initial denaturationa

95

10 min

1

Denaturation

95

30 sec

25~35

Annealingb

55~65

30~60 sec

Elongation

72

1 min/kb

Final elongation

72

5 min

1

When cycles are over, keep the reaction at 4; may add 10 mM EDTA until use to prevent DNA degradation

aAt least 10 min of initial denaturation time is required to fully activate the chemically modified PCR DNA polymerase

bRecommend annealing temperature is 5 to 10 below the lower Tm of the two primers used.

 

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