Gel extraction manual qiagen






















1. Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. 2. Weigh the gel slice in a colorless tube. Add 3 volumes Buffer QG to 1 volume gel ( mg gel ~ μl). The maximum amount of gel per spin column is mg. For 2% agarose gels, add 6 volumes Buffer QG. www.doorway.ru Size: 44KB. QIAquick® PCR Purification Kit QIAquick® PCR Gel Cleanup Kit The QIAquick PCR Purification Kit and the QIAquick PCR Gel Cleanup Kit (cat. nos. , , and ) can be stored at room temperature (15–25°C) for up to 12 QIAGEN kit handbook or user manual. Jamal Moya on __TOP__ Qiaquick Gel Extraction Kit Manual Pdf. QIAquick Gel Extraction Kit En - Free download as PDF File .pdf), Text File .txt) or read This protocol is for the purification of up to 10 g DNA (70 bp to 10 kb).


1. Excise the DNA fragment from the agarose gel with a clean, sharp scalpel. Minimize the size of the gel slice by removing extra agarose. 2. Weigh the gel slice in a colorless tube. Add 3 volumes of Buffer QG to 1 volume of gel ( mg ~ µl). For example, add µl of Buffer QG to each mg of gel. For 2% agarose gels, add 6 volumes of Buffer QG. PCR Purification Nucleotide Gel Extraction Kit Removal Kit Kit Maximum binding capacity: 10 µg 10 µg 10 µg Maximum weight of gel slice: — mg Minimum elution volume: 30 µl 30 µl 30 µl Capacity of column reservoir: µl µl µl Typical recoveries Recovery of DNA: 90–95% 80–95% 70–80%. Each fragment was manually excised from the agarose gel and processed using the Monarch DNA Gel Extraction Kit. The entire elution of each fragment was resolved on a new gel with the remainder of the original mixture for comparison. DNA purified from agarose gels using the Monarch DNA Gel Extraction Kit can be reproducibly isolated and ligated.


Silica columns from PCR purification and gel extraction kits are widely used residual DNA from used Qiagen PCR purification kit columns. The QIAquick Gel Extraction protocol works equally well with standard or low melting point agarose gels in TBE or TAE buffers. QIAquick PCR Purification and. This process forms the basis for rudimentary genetic engineering. Practice. We used the QIAgen quick gel extraction kit, the protocol is adapted from the.

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