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Nucleospin rna plant and fungi mini kit

Manufactured by Macherey-Nagel
Sourced in Germany

The NucleoSpin RNA Plant and Fungi Mini Kit is a laboratory equipment designed for the efficient extraction and purification of high-quality RNA from plant and fungal samples. The kit utilizes a convenient column-based system to isolate total RNA, which can be subsequently used in various downstream applications.

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3 protocols using nucleospin rna plant and fungi mini kit

1

Genomic and Transcriptomic DNA/RNA Extraction

Check if the same lab product or an alternative is used in the 5 most similar protocols
For genomic DNA extraction, cultured cells were lysed with Westase (Ozeki, Japan) following the manufacturer’s instructions for Saccharomyces cerevisiae. Genomic DNA was extracted following Westase’s protocol provided by the distributor (Takara, Japan). Isolated DNA was purified using Genomic-tip 20/G columns (Qiagen, Netherlands). For RNA extraction, cells were twice disrupted using a vortex mixer with glass beads for 30 s. RNA was extracted using a NucleoSpin RNA Plant and Fungi Mini Kit (Macherey-Nagel, Germany) following the manufacturer’s instructions.
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2

Genomic and Transcriptomic DNA/RNA Extraction

Check if the same lab product or an alternative is used in the 5 most similar protocols
For genomic DNA extraction, cultured cells were lysed with Westase (Ozeki, Japan) following the manufacturer’s instructions for Saccharomyces cerevisiae. Genomic DNA was extracted following Westase’s protocol provided by the distributor (Takara, Japan). Isolated DNA was purified using Genomic-tip 20/G columns (Qiagen, Netherlands). For RNA extraction, cells were twice disrupted using a vortex mixer with glass beads for 30 s. RNA was extracted using a NucleoSpin RNA Plant and Fungi Mini Kit (Macherey-Nagel, Germany) following the manufacturer’s instructions.
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3

Genomic and Transcriptomic DNA/RNA Extraction

Check if the same lab product or an alternative is used in the 5 most similar protocols
For genomic DNA extraction, cultured cells were lysed with Westase (Ozeki, Japan) following the manufacturer’s instructions for Saccharomyces cerevisiae. Genomic DNA was extracted following Westase’s protocol provided by the distributor (Takara, Japan). Isolated DNA was purified using Genomic-tip 20/G columns (Qiagen, Netherlands). For RNA extraction, cells were twice disrupted using a vortex mixer with glass beads for 30 s. RNA was extracted using a NucleoSpin RNA Plant and Fungi Mini Kit (Macherey-Nagel, Germany) following the manufacturer’s instructions.
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