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此商品 | 101406 | 146435 | 103854 |
|---|---|---|---|
| suitability enterobacteriaceae | suitability coliforms | suitability enterobacteriaceae | suitability selective and differential for Vibrio spp. |
| technique(s) microbiological culture: suitable | technique(s) microbiological culture: suitable | technique(s) - | technique(s) microbiological culture: suitable |
| form medium granules (dehydrated (DCM)) | form medium granules (dehydrated (DCM)) | form - | form powder |
| application(s) food and beverages | application(s) food and beverages | application(s) food and beverages | application(s) food and beverages |
| pH 7.3 (37 °C, 40 g/L in H2O, after autoclaving) | pH 7.3-7.5 (37 °C, 40 g/L in H2O, after autoclaving) | pH 7.6 ( in H2O) | pH 8.6±0.2 (25 °C) |
一般描述
Recover 100 to 10,000 bp DNA from agarose gel slices in a single 10-minute spin. The kit consists of a pre-assembled filter device with an agarose gel nebulizer, a microcentrifuge vial, and modified TAE gel extraction buffer (dry).
The device utilizes gel compression to extract DNA from the agarose. Centrifugal force collapses the gel structure, drives the agarose through a small orifice in the gel nebulizer and the resultant gel slurry is sprayed into the sample filter cup.
Prepared DNA requires no further purification for most applications, including cloning and radioisotopic or fluorescent DNA sequencing. Since agarose gel electrophoresis has high resolving power, the small and large non-specific amplification products that frequently interfere with cloning and sequencing after PCR are completely removed from the product.
Performance
100 78
700 71
1000 77
2027 47
4361 35
9416 32
23130 29
Protocol
1. Excise the band of interest after routine electrophoretic analysis of PCR products or other DNA through an agarose gel.
2. Place the gel slice into the pre-assembled device. Note: Protocol is not compatible with low melting point agarose.
3. Spin at 5,000 x g for 10 minutes to extract gel slurry into filter cup.
4. DNA can be stored in the capped filtrate vial after discarding the sample filter cup and gel nebulizer.
The device utilizes gel compression to extract DNA from the agarose. Centrifugal force collapses the gel structure, drives the agarose through a small orifice in the gel nebulizer and the resultant gel slurry is sprayed into the sample filter cup.
Prepared DNA requires no further purification for most applications, including cloning and radioisotopic or fluorescent DNA sequencing. Since agarose gel electrophoresis has high resolving power, the small and large non-specific amplification products that frequently interfere with cloning and sequencing after PCR are completely removed from the product.
- Minimal hands-on time
- 10-minute spin
- Fully-functional DNA
Performance
Typical DNA Recoveries from Agarose Gels
DNA Size (bp) Percent DNA Recoveries
100 78
700 71
1000 77
2027 47
4361 35
9416 32
23130 29
Protocol
1. Excise the band of interest after routine electrophoretic analysis of PCR products or other DNA through an agarose gel.
2. Place the gel slice into the pre-assembled device. Note: Protocol is not compatible with low melting point agarose.
3. Spin at 5,000 x g for 10 minutes to extract gel slurry into filter cup.
4. DNA can be stored in the capped filtrate vial after discarding the sample filter cup and gel nebulizer.
组分
包含 50 个 Ultrafree-DA 装置和 500 mL 的 50x 浓缩
改良 TAE 缓冲液
改良 TAE 缓冲液
法律信息
MONTAGE is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
10 - Combustible liquids
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相关内容
We manufacture IP and antibody purification agarose beads that purify immunoglobulins and IgG fractions. Our kits also provide a total antibody purification process
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