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Red Load Taq Master (5x)

Kód produktu: PCR-108L Kód výrobce: PCR-108L Výrobce: Jena Bioscience GmbH
6 640,66 Kč
5 488,15 Kč bez DPH
do týdne

Red Load Taq Master (5x)
Master mix for direct gel loading

Zobraz detailní popis

Detailní popis

For in vitro use only!

Shipping: shipped on blue ice

Storage Conditions: store at -20 °C
avoid freeze/thaw cycles

Shelf Life: 12 months

Form: liquid

Concentration: 5x conc.

Description:
Red Load Taq Master contains an inherent red dye and allows the direct loading of the PCR reaction product onto the gel. It contains all reagents required for PCR (except template and primer) in a premixed 5x concentrated ready-to-use solution.
The Master Mix is recommended for use in routine PCR reactions. It is optimized for high specificity and guarantees minimal by-product formation. The mix is particularly suitable for plate based PCR and automated pipetting where a detergent free buffer system is required.
The enzyme catalyzes the polymerization of nucleotides into duplex DNA in 5'→3' direction in the presence of magnesium. It also possesses a 5'→3' polymerization-dependent exonuclease replacement activity but lacks a 3'→5' exonuclease activity.

Content:
5x Red Load Taq Master (red cap)
master mix of thermostable DNA polymerase, dATP, dCTP, dGTP, dTTP, KCl, MgCl2, red dye, gel loading buffer and stabilizers.

PCR grade water (white cap)

Recommended 50 μl PCR assay:

10 μl 5x Taq Master Mix red cap
0.2 - 1 μM each Primer -
2 - 50 ng Template DNA -
Fill up to 50 μl PCR grade Water white cap

Recommended cycling conditions:
Initial
denaturation
94 °C 2 min 1x
Denaturation 94 °C 30 sec 30x
Annealing1) 45 - 68 °C 30 sec 30x
Elongation2) 72 °C 30 sec - 3 min 30x
Final
elongation
72 °C 2 min 1x

1) The annealing temperature depends on the melting temperature of the primers used.
2) The elongation time depends on the length of the fragments to be amplified. A time of 1 min/kb is recommended.

 

For optimal specificity and amplification an individual optimization of the recommended parameters may be necessary for each new template DNA and/or primer pair.

 

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