- ￥1500 - 1700
- Eppendorf
- 3120 000.216
- 2025年07月14日
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- 详细信息
- 询价记录
- 文献和实验
- 技术资料
- 库存：
111
- 规格：
0.1–2.5 μl
| 量程（货号） | 体积 | 系统误差 | 随机误差 | ||
| 0.1–2.5 μl（3120000216） | 0.25 μl | ±12.0% | ±0.03 μl | ±6.0% | ±0.015 μl |
| 1.25 μl | ±2.5% | ±0.031 μl | ±1.5% | ±0.019 μl | |
| 2.5 μl | ±1.4% | ±0.035 μl | ±0.7% | ±0.018 μl | |
| 0.5 - 10 μl（3120000224） | 0.5 μl | ±8.0% | ±0.04 μl | ±5.0% | ±0.025 μl |
| 1 μl | ±2.5% | ±0.025 μl | ±1.8% | ±0.018 μl | |
| 5 μl | ±1.5% | ±0.075 μl | ±0.8% | ±0.04 μl | |
| 10 μl | ±1.0% | ±0.1 μl | ±0.4% | ±0.04 μl | |
| 2–20 μl（3120000232） | 2 μl | ±5.0% | ±0.1 μl | ±1.5% | ±0.03 μl |
| 10 μl | ±1.2% | ±0.12 μl | ±0.6% | ±0.06 μl | |
| 20 μl | ±1.0% | ±0.2 μl | ±0.3% | ±0.06 μl | |
| 10–100 μl（3120000240） | 10 μl | ±3.0% | ±0.3 μl | ±1.0% | ±0.1 μl |
| 50 μl | ±1.0% | ±0.5 μl | ±0.3% | ±0.15 μl | |
| 100 μl | ±0.8% | ±0.8 μl | ±0.2% | ±0.2 μl | |
| 20–200 μl（3120000259） | 20 μl | ±2.5% | ±0.5 μl | ±0.7% | ±0.14 μl |
| 100 μl | ±1.0% | ±1.0 μl | ±0.3% | ±0.3 μl | |
| 200 μl | ±0.6% | ±1.2 μl | ±0.2% | ±0.4 μl | |
| 30–300 μl（3120000305） | 30 μl | ±2.5% | ±0.75 μl | ±0.7% | ±0.21 μl |
| 150 μl | ±1.0% | ±1.5 μl | ±0.3% | ±0.45 μl | |
| 300 μl | ±0.6% | ±1.8 μl | ±0.2% | ±0.6 μl | |
| 100–1000 μl（3120000267） | 100 μl | ±3.0% | ±3.0 μl | ±0.6% | ±0.6 μl |
| 500 μl | ±1.0% | ±5.0 μl | ±0.2% | ±1.0 μl | |
| 1.000 μl | ±0.6% | ±6.0 μl | ±0.2% | ±2.0 μl | |
| 0.5–5 ml（3120000275） | 0.5 ml | ±2.4% | ±0.012 ml | ±0.6% | ±0.003 ml |
| 2.5 ml | ±1.2% | ±0.03 ml | ±0.25% | ±0.006 ml | |
| 5 ml | ±0.6% | ±0.03 ml | ±0.15% | ±0.008 ml | |
| 1–10 ml（3120000283） | 1 ml | ±3.0% | ±0.03 ml | ±0.6% | ±0.006 ml |
| 5 ml | ±0.8% | ±0.04 ml | ±0.2% | ±0.01 ml | |
| 10 ml | ±0.6% | ±0.06 ml | ±0.15% | ±0.015 ml | |
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- 作者
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文献和实验Fast and reliable mini-prep RNA extraction from Neurospora crassa
were stamped out using an inverted Pasteur pipette and frozen. The procedure of extraction given below is described for Eppendorf tubes but it is also possible to scale up the volumes. All manipulations were performed at room temperature if not stated
Rapid Extraction of High Quality DNA from Whole Blood Stored at 4ºC for Long Period
should be shake gently by rotating blood mixer (vortex) Pour 500 µl of blood into a 1.5 ml eppendorf tube and add 1000 µl of red cell lysis buffer. Shake microfuge tube gently (up to homogenizing), then spin for 2 minutes at 7000 rpm. Discard
Chromatin IP (CHIP assay) This protocol has some minor modification to the protocol described in Strahl-Bolsinger S. et al. [1997, Gen & Dev 11, p83-93] and was obtained from Flick K. (The Scripps Research Institute).
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