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    Immunostaining on Paraffin Sections of Fly Heads

    Mel Feany

    Published: 2022-10-25 DOI: 10.17504/protocols.io.81wgby61nvpk/v2
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    Abstract

    This protocol describes how to perform immunostaining on paraffin sections of fly heads.

    Steps

    1.

    Fix fly heads overnight in 4% formalin.

    2.

    Embed in paraffin.

    3.

    Cut 4 micron sections.  Dry at 42°C .

    4.

    Deparaffinize and bring through ethanols to water (xylene x 2, 100% ethanol x 4, tap H2O x 2).

    5.

    Microwave slides in 10millimolar (mM) sodium citrate for 0h 15m 0s.

    Cool 0h 20m 0s .

    Stock: 100millimolar (mM) sodium citrate, pH 6.0

    Use at least 1L of citrate solution in large glass box to avoid drying.

    6.

    Block in PBST (PBS with 0.3% Triton) with 2% dry milk for 0h 30m 0s

    Stock: 10X PBS

    7.

    Incubate with primary antibody at Room temperature .

    8.

    Wash 3 x in PBST.

    9.

    Incubate with appropriate biotinylated secondary (for immunohistochemistry) or fluorescent secondary (for immunofluorescence) antibody at 1:200 in PBST + milk for 1h 0m 0s at Room temperature .

    For immunohistochemistry incubate in ABC reagent (Vector) for 1h 0m 0s at Room temperature .

    10.

    Rinse 3 x PBST.

    11.

    Mount slides with antifading medium for immunofluorescence or dehydrate through ethanol series and xylenes and mount in Permount for immunohistochemistry.

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