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제품 설명
2X AmPelify™ PCR Master Mix
제품 번호
BR0101001
제품 특징
Description
biotechrabbit™ 2X AmPelify PCR Master Mix is a perfect choice for a fast reaction setup that reduces the time required for calculation and pipetting and eliminates the need for buffer optimization. It is designed for high yield of the products in routine, high-throughput PCR amplification of 0.2–5 kb DNA targets. The 2X AmPelify PCR Master Mix contains highly purified recombinant biotechrabbit Taq DNA Polymerase, extremely high-quality dNTPs and optimized PCR buffer; thus, only template, PCR primers and PCR Grade Water need to be added.
biotechrabbit Taq DNA polymerase is a thermostable, highly processive 5'→3' DNA polymerase that has low 5'→3' exonuclease activity and lacks 3'→5' exonuclease (proofreading) activity. The latter allows incorporation of modified nucleotides.
The enzyme also exhibits deoxynucleotidyltransferase activity that results in the addition of extra A overhang at the 3' ends of PCR products, allowing easy cloning of PCR products into vectors with T overhangs.
Other Information
Quality ControlFunctional assayHuman genomic DNA was amplified using the 2X Ampelify PCR Master Mix and specific primers to produce a distinct band. |
Protocols
When assembling the amplification reactions, care should be taken to eliminate the possibility of contamination with undesired DNA.
The standard PCR protocol using biotechrabbit reaction buffer provides excellent results for most applications. Optimization might be necessary for certain conditions, such as the amplification of long targets, high GC or AT content, strong template secondary structures or insufficient template purity. In such cases, optimization of template purification (see biotechrabbit nucleic acid purification kits), primer design and annealing temperature is recommended.
The best conditions for each primer-template can be optimized with the following:
Component | Volume | Final concentration |
PCR Master Mix, 2× | 25 µl | 1× |
Forward primer | Variable | 0.2–1 µM |
Reverse primer | Variable | 0.2–1 µM |
Template DNA | Variable | 10 pg–1 μg |
| Use 0.01–1 ng for plasmid or phage DNA and 0.1–1 μg for genomic DNA | |
Nuclease free water | Variable |
|
Total volume | 50 µl |
|
Step | Temperature | Time | Cycles |
Initial activation | 95°C | 2 min | 1 |
Denaturation | 95°C | 30 s | 25–35 |
Annealing* | (55-68°C) | 15–30 s | 25–35 |
| *Recommended annealing temperature is 2°C above Tm of primers, | ||
Extension | 72°C | 30–60 s/kb | 25–35 |
Final extension | 72°C | 5 min | 1 |
| To extend all incomplete PCR products | ||
Storage in the cycler | 4°C | Indefinitely | 1 |
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