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Taq DNA Polymerase 1000U

Taq DNA Polymerase 1000U
New
Taq DNA Polymerase 1000U
$99.00
Ex Tax: $99.00
  • Stock: In Stock
  • Model: 0460

Product Introduction


Assay Protocol

 Routine PCR Protocol

1. Reaction setup:

We recommend assembling all reaction components on ice and quickly transferring the reactions to a thermocycler preheated to the denaturation temperature (95°C).

Component

Volume

10× Reaction buffer

5 μL

Taq DNA polymerase

0.5 μL(variable

dNTP Mix (10 mM each)

1 μL

Forward primer/Reverse primer (10 μM)

2 μL/2 μL

Template

Variable (0.1-50 ng)

Nuclease-Free water

To 50 μL

It could be added to no more than 10% DMSO to the reaction system for high GC templates.

The reaction volumes can be scaled up or down providing that the final concentrations of the components (DNA, dNTPs, labeled dNTP) are as indicated in the protocol.

2. Gently vortex the samples and spin down.

3. Perform PCR using the recommended thermal cycling conditions outlined below:

Step

Temperature

Time

Number ofCycles

Initial Denaturation

95℃

3 min

1

Denaturation

95℃

15-30 s

25-35

Annealing

50-68℃

15-30 s

Extension

72℃

1 min/kb

Final extension

72℃

5-10 min

1

Note

1. It is recommended that thereaction system should be prepared on ice.

2. The optimization of PCR reactions can be adjusted from Mg2+ concentration, template amount, enzyme amount, annealing temperature, etc.

3. For your safety and health, pleasewearsafety glasses, gloves, or protective clothing.

 

For Research Use Only!

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