製品概要
PCR amplification of DNA fragments, DNA labeling, primer extension, sequence determination, blunt end addition of A, TA vector cloning
| 商品情報 | |
|---|---|
| 分子量 | 94 K D |
| Polymerase Activity | 5′-3′ DNA polymerase, 5′-3′ exonuclease (no 3′-5′ exonuclease) |
| PCR Buffer | 10 X PCR Buffer for direct loading |
| Experimental Efficiency | The PCR reaction can be directly detected by electrophoresis |
| Extension Speed | 1-2 kb/min |
| Terminal Base | Product has A at the 3′ end, facilitating TA vector cloning |
| Reaction System (20μl) | Addition Amount | Remarks |
|---|---|---|
| Pure DNA Polymerase | 0.8μl | Adjust for amplification needs |
| 10x PCR Buffer | 2μl | |
| dNTP (2.5mM) | 2μl | |
| PrimerF | 0.1-1μl | 10-50pmol used |
| PrimerR | 0.1-1μl | 10-50pmol used |
| Template | <1μg | |
| ddH2O | Up to 20μl |
| Cycle Program | Temperature (℃) | Time | Remarks |
|---|---|---|---|
| Initial Denaturation | 94 | 3分 | |
| 変性 | 94 | 30s (30-40 サイクル) | |
| アニーリング | 45-60 | 30s | |
| 拡大 | 72 | 30s-2min | Extension time varies with fragment |
| Final Extension | 72 | 10分 |
手順
Can be directly detected without adding a Loading Buffer
Result Detection
After PCR, 取る 5 μl of product for agarose gel electrophoresis
レビュー
まだレビューはありません.