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    Quick-DNA Fungal/Bacterial 96 Kit


    Quick-DNA Fungal/Bacterial 96 Kit

    Cat # Name Size
    D6006 Quick-DNA Fungal/Bacterial 96 Kit 2 x 96 Preps



    • Boost Detection: Included BashingBeads ensure complete lysis of tough-to-lyse samples.
    • Ultra-Pure: Ready for qPCR, Next-Gen Sequencing, arrays, etc.
    • Simple: Fastest high-throughput workflow (≤ 40 minutes).

    The Quick-DNA Fungal/Bacterial 96 Kit is designed for the simple and rapid isolation of DNA from tough-to-lyse fungi, including A. fumigatus, C. albicans, N. crassa, S. cerevisiae, S. pombe, as well as Gram (+/-) bacteria, algae, and protozoa. The procedure is easy and can be completed in minutes: fungal and/or bacterial samples are rapidly and efficiently lysed with our state of the art, ultra-high density BashingBeads. Zymo-Spin column technology is then used to isolate the DNA that is ideal for downstream molecular-based applications including PCR, array, etc.

    Applicable For All sensitive downstream applications such as qPCR and Next-Generation Sequencing.
    Elution Volume ≥ 25 µl
    Equipment Centrifuge with microplate carriers, 96-well plate/block disruptor or pulverizer.
    Processing Time ≤ 40 minutes
    Processing Volume ≤20 mg (wet weight) fungi or bacteria, 2x108 bacterial cells, 2x107 yeast cells, or 2x107 mammalian cells
    Purity Typical A260/A280 & A260/A230 ≥ 1.8
    Sample Source Fungal and bacterial cell cultures, spores, pollen, nematodes, as well as other microorganisms can also be sampled.
    Size Range Capable of recovering genomic DNA sized fragments from up to and above 40 kb. Typical fragment sizes range from 25 kb - 35 kb. If present, parasitic and viral DNA will also be recovered.
    Supplemental Info
    Type Total DNA
    Yield ≤ 5 µg total DNA

    A viscous sample can indicate incomplete sample lysis. Try using less of your sample and optimize bead beating conditions (duration, speed, time) to ensure samples are thoroughly lysed. After bead beating, pellet the cell debris before moving on. Adding more Genomic Lysis buffer to the lysate can help dilute and deproteinate the sample, making the sample less viscous and more suitable for DNA recovery.

    Addition of beta-mercaptoethanol is recommended to enhance sample lysis, but can be substituted with dithiothreitol (DTT, final concentration of 10 mM). However, if bead beating is optimized and lysis is efficient, the addition of BME is not necessary and can be omitted.

    No additional RNase A treatment is required when processing samples within kit capacity. The selective chemistry allows for binding of double stranded DNA to the column and for RNA to flow through.

    Cat # Name Size
    S6002-96-3 ZR-96 BashingBead Lysis Rack 0.5 mm & 0.1 mm
    C2003 Elution Plate 2 Plates
    C2002 Collection Plate 2 Plates
    C2001 Silicon-A Plate 2 Plates
    P1001-2 96-Well Block 2 Blocks
    C2007-4 96-Well Plate Cover Foil 4 Foils
    D6001-3-40 BashingBead Buffer 40 ml
    D3004-5-50 DNA Pre-Wash Buffer 50 ml
    D3004-1-150 Genomic Lysis Buffer 150 ml
    D3004-2-100 g-DNA Wash Buffer 100 ml
    D3004-4-10 DNA Elution Buffer 10 ml