- No products in the cart.
Applications
- Routine PCR up to 6 kb with a direct gel loading option
- PCR of GC rich templates
- Colony PCR, Fast PCR, TA cloning
Benefits
- Premixed with the dye and density reagent for direct loading on the gels
- Higher yields under standard and fast cycling
- Success with longer (6 kb) and GC rich templates
highQu ALLin™ Taq DNA Polymerase is the versatile engineered enzyme which in combination with the optimized ALLin™ buffer provides higher success rates in demanding PCR applications like amplification of complex templates, crude sample PCR and fast cycling. ALLin™ Taq DNA Polymerase has the same PCR accuracy like Taq DNA Polymerase, 4.5 x 104 (a number of correct nucleotides incorporated before the error occurs) and produces A-tailed products suitable for ligating into TA cloning vectors.
The convenience of ALLin™ Taq DNA Polymerase is maximized by the use of 2X Red Mastermix providing the additional advantage of reduced pipetting and minimized errors.
ALLin™ Red Taq Mastermix, 2X is premixed with red dye and density reagents for direct loading on the gels after the PCR.
In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose TAE gel with ~ 600 bp DNA fragments.
The mastermix is even supplied with the PCR Water, and the only thing to add is the template with primers.
mportant Notes
- Take typical measures to prevent PCR cross over contamination, keep your bench clean, wear gloves, use sterile tubes and filter pipet tips.
- Include a no-template control and positive control in parallel.
- Thaw and keep reagents on ice. Mix well before use.
- The longer the amplicon, the longer the extension time: 15 sec/kb - <6kb and 1 sec/kb - <1kb. Use >90 sec extension for multiplexing
- Run an annealing temperature gradient from 55°C to 65°C to choose the best specificity conditions.
- Do not use fast cycling for multiplexing.
Prepare a 50 µl PCR reaction
| Rev. & For. Primers | variable, up to 0.4 µM final each (2 µl of 10 µM each) |
|
cDNA Template or gDNA Template |
<100 ng or 5 - 500 ng |
| PCR Water | to 25 μl |
| ALLin™ Red Taq Mastermix, 2X | 25 µl |
- Mix gently, avoid bubbles.
- Place into the instrument set like:
| Initial denaturation | 1 cycle: 95°C - 1 min |
| Denaturation | 40 cycles: 95°C - 15 sec |
| Annealing | 40 cycles: 55-65°C - 15 sec |
| Extension | 40 cycles: 72°C – 1 - 90 sec (15 sec/kb) |
-
Load probes on the agarose gel. The red loading dye is included in the mastermix.
-
ALLin™ Red Taq Mastermix, 2X is premixed with red dye and density reagents for direct loading on the gels after the PCR. In a 2% agarose TAE gel the dye migrates with~350 bp DNA, in 1% agarose TAE gel with ~ 600 bp DNA fragments.
- Store probes on ice shortly, store at -20°C for long term.
|
Cat. |
Size |
Components |
Composition |
|
| PCM0201 |
200 r of 50 µl |
5 x 1 ml - ALLin™ Red Taq Mastermix, 2X 5 x 1 ml - PCR Water |
1X mastermix contains 0.25 mM dNTPs, 3 mM MgCl2, enhancers, stabilizers, red electrophoresis tracking dye and density reagents for gel loading |
|
| PCM0205 |
1000 r of 50 µl |
25 x 1 ml - ALLin™ Red Taq Mastermix, 2X 25 x 1 ml - PCR Water |
1X mastermix contains 0.25 mM dNTPs, 3 mM MgCl2, enhancers, stabilizers, red electrophoresis tracking dye and density reagents for gel loading |
|
|
Storage |
In the dark at -20°C. |
|||
