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AccuAmp Fast SYBR® Green qPCR Master Mix

Cat. No.

Size

Price

Quantity

11018-100

100 x 25-µl reactions (1.25 ml)

$89.00

11018-400

400 x 25-µl reactions (4 x 1.25 ml)

$309.00

11018-01k

1000 x 25-µl reactions (12.5 ml)

$729.00

11018-02k

2000 x 25-µl reactions (25 ml)

$1359.00

 

Benefits

Description

AccuAmp Fast SYBR® Green qPCR Master Mix is a 2X concentrated, ready-to-use reaction cocktail that contains all components, except primers and template, for rapid real-time PCR on a variety of instruments that do not require a reference dye. This master mix provides highly specific and sensitive real-time quantification of genomic DNA and cDNA targets using SYBR® Green I, under fast cycling conditions. Since SYBR® Green dye binds to all double-stranded DNA, it is crucial to reduce/ avoid any nonspecific products and primer–dimers generated during amplification. AccuAmp Fast SYBR® Green qPCR Master Mix promotes highly specific annealing of primers to the PCR template through our unique combination of proprietary buffer, stabilizers, and specially modified hot-start Taq DNA polymerase, which prevents any polymerase activity before heat activation, thereby eliminating amplification of nonspecific products.

Compatible Instrument

Storage

AccuAmp Fast SYBR® Green qPCR Master Mix is stable for 1 year when stored at –20°C in a constant-temperature freezer, protected from light.  After thawing, mix thoroughly before using.

Quick-Reference Protocol

1. Thaw AccuAmp Fast SYBR Green qPCR Master Mix (2X), template, and primers. Mix the individual solutions.

2. Prepare a reaction mix.

Component

Volume/Reaction

Final Concentration

AccuAmp Fast SYBR Green qPCR
Master Mix(2X)

12.5 µl

1X

Forward Primer

Variable

300 nM

Reverse Primer

Variable

300 nM

Template DNA or cDNA

Variable

Up to 100 ng/reaction

Nuclease-free Water

Variable

 

Total Reaction Volume

25 µl

 

 

3. Mix the reaction mix thoroughly. After sealing each reaction, centrifuge reaction tubes briefly to avoid bubbles.

4. Program your thermal cycler.

Step

Temperature &Time

Notes

PCR initial activation step

95°C, 10 min

Hot-start Taq DNA polymerase is activated by this heating step.

2-step cycling (40 cycles)*

a. 95°C, 10 sec (Denaturation)
b. 60°C, 30 sec (Annealing/Extension)

Collect fluorescence data at step b.

Melting curve analysis

Refer to instrument instructions

Strongly recommended

 

* The primer Tm may be above or below the temperature of annealing/extension.  As a starting point, use primers with Tm 60-65ºC.

5. Place the PCR tubes or plates in the real-time cycler, and start the cycling program.

6. Follow instruction provided by the cycler supplier, and perform a melting curve analysis of the PCR product(s).