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    Qiagen DNeasy 96 blood & tissue protocol for bee guts

    Lauren Ponisio, Jocelyn Zorn

    Published: 2022-11-03 DOI: 10.17504/protocols.io.q26g78k23lwz/v1
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    Abstract

    Tissue protocol for bee guts.

    Steps

    Day 1

    1.

    UV sterilize supplies for 2 96 well plates worth of extractions: 1 50mL centrifuge tube, 1 15mL centrifuge tube, 1 box 1,000uL pipette tips, 2 boxes 200uL pipette tips, 24 elution microtube strip caps, steel beads, zirconia beads, and 1 reagent reservoir

    2.

    Combine 36mL and 4000µL in 50mL centrifuge tube, invert gently to mix

    3.

    Add 200µL ATL + Proteinase K solution to each sample

    4.

    Add ~100µL zirconia beads and 2 steel beads to each sample

    5.

    Place plates in tissue lyser and run at 30Hz for 0h 2m 30s, then rotate plates 180 degrees and lyse at 30Hzfor an additional 0h 2m 30s

    Equipment

    ValueLabel
    TissueLyser IINAME
    Bead MillTYPE
    QIAGENBRAND
    85300SKU

    Equipment

    ValueLabel
    TissueLyser Adapter Set 2 x 96NAME
    Adapter setTYPE
    QiagenBRAND
    69984SKU
    6.

    Centrifuge on "short" for 0h 0m 7s then shake by hand for 0h 0m 15s

    Equipment

    ValueLabel
    Eppendorf™ 5810R CentrifugeNAME
    CentrifugeTYPE
    EppendorfBRAND
    02-262-8187SKU
    7.

    Incubate 56°C for 1h 0m 0s with weight on top of plate

    Note: remove from incubator carefully with weight on top so that caps do not pop off

    8.

    Place plates in tissue lyser and run at 30Hz for 0h 1m 0s

    9.

    Incubate 56°C overnight with weight on top of plate

    Day 2

    10.

    UV sterilize supplies: 4 reagent reservoirs, 24 elution microtube strip caps (clear), 2 boxes 1,000uL tips (plus some extra), 6 boxes 200uL tips (plus some extra), 2 s-blocks, 2 elution microtube plates (dark blue) and 24 strip caps (white), and 6 96 well microplates (for aliquotting final product). Label 6 foil microplate lids for aliquots

    11.

    Carefully remove plates from incubator, leaving the weight on top, and allow to sit at room temperature for a few minutes before carefully removing weight to ensure strip caps do not pop off

    12.

    Shake plates by hand for 0h 0m 15s , rotating plates halfway through

    13.

    Centrifuge on "short" for 0h 0m 7s

    14.

    Add 410µL ALE to each sample

    15.

    Seal with new caps and shake by hand for 0h 0m 15s , rotating plates halfway through

    16.

    Centrifuge on "short" for 0h 0m 7s

    17.

    Place DNeasy filter plates on top of s-blocks

    18.

    Transfer lysate to DNeasy filter plate and seal with AirPore tape

    19.

    Centrifuge 3486x g . Discard flowthrough

    20.

    Add 500µL to each sample, seal with AirPore tape

    Safety information
    Buffer AW1 contains guanidine salt - do not mix with bleach

    21.

    Centrifuge 3486x g . Discard flowthrough

    22.

    Add 500µL , do not seal

    Safety information
    Manage and dispose of buffer AW2 as hazardous waste

    23.

    Centrifuge 3486x g . Discard flowthrough

    24.

    Repeat steps 22 and 23

    25.

    Place DNeasy filter plate on top of elution microtube plate (dark blue)

    26.

    Add 55µL to each sample

    27.

    Incubate at room temperature for 0h 1m 0s

    28.

    Centrifuge 3486x g

    29.

    Aliquot entirety of product into 3 96 well microplates per DNA plate, seal with labeled foil lids and store at -20°C

    30.

    For a second backup elution, add 50µL to each sample

    31.

    Incubate at room temperature for 0h 1m 0s

    32.

    Centrifuge 3486x g

    33.

    Seal with white strip caps

    34.

    Store at -20°C

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