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        Basic Fluorescent in situ Hybridization (FISH)

        互联网

        1080

        实验试剂

         

         

        20x Saline-sodium citrate buffer [ Details SSC: 3 M NaCl, 0.3 M sodium citrate, pH 7, or Product No. S6639].

         

        RNase A   [ Details Product No. R4642] 100 µg/ml in 2x SSC.

         

        Pepsin [ Details Product No. P6887] 40 units/ml in 10 mM HCl.

         

        Paraformaldehyde, EM grade [ Details Product No. P6148] freshly depolymerized, 4% w/v in water.

         

        Ethanol.

         

        Labeled probe. Plasmid DNA is labeled with biotin-11-dUTP using nick translation random priming or the polymerase chain reaction

         

        Hybridization mix solution: 50% formamide [ Details Product No. F7508], 10% dextran sulfate [ Details Product No. D8906], 0.1% SDS [ Details Product No. L4390], 0.5-1.5 ng/µl labeled probe and 300 ng/ml Salmon Sperm DNA [ Details Product No. D7656] in 2x SSC.

         

        Wash buffer: 20% formamide [ Details Product No. F7508] in 0.1x SSC.

         

        Detection buffer: 0.2% Tween 20 [ Details Product No. P1379] in 4x SSC.

         

        Blocking buffer: 5% bovine albumin [ Details Product No. A3803] in detection buffer.

         

        Antibody or detection compound [ Details e.g., Streptavidin-Cy3, Product No. S6402] in blocking buffer.

         

        DAPI [ Details Product No. D9542]   2 µg/ml in antifade mounting medium.

         

        实验设备

         

         

        Heat block/ modified thermocycler.

         

        Coplin jars for washing steps [ Details Product No. S6016, S5641 or S5891].

         

        Fluorescence microscope, filters and optional triple band pass filter [ Details x58, Omega Optics].

         

        实验材料

         

         

        Plastic cover slips for incubation and hybridization steps [ Details cut from autoclavable waste bags, e.g., Product No. B4408]

         

        Glass slides [ Details Product No. S8400].

         

        实验步骤

         

         

        1.        Slide Preparation

         

        1)   Start with chromosome preparations from any cell type.

         

        2)   Incubate with 200 µl RNase for 1 hour at 37 °C

         

        3)   Wash slides in 2x SSC for 5 minutes, repeat.

         

        4)   Rinse slides in 10 mM HCl.

         

        5)   Incubate with 200 µl pepsin for 10 minutes at 37 °C.

         

        6)   Rinse slides in deionized H2O.

         

        7)   Wash slides in 2x SSC for 5 minutes, repeat.

         

        8)   Stabilize slides in paraformaldehyde for 10 minutes.

         

        9)   Wash slides in 2x SSC for 5 minutes, repeat.

         

        10)           Dehydrate slides in an ethanol series: 70%, 80%, 95%; 2 minutes each.

         

        11)           Air dry.

         

        2.        Hybridization

         

        Prepare 30 µl hybridization solution per slide. Heat to 70 °C. for 10 minutes and place on ice.

         

        Place 30 µl of hybridization solution on each slide and cover with a plastic cover slip.

         

        Denature slide at 65-70 °C for 5 minutes on heat block.

         

        Gradually decrease temperature to 37 °C.

         

        Hybridize at 37 °C overnight in humidity chamber.

         

        3.        Detection

         

        1)   Wash slides in 2x SSC to remove coverslip.

         

        2)   Wash slides in wash buffer at 40 °C for 5 minutes, repeat.

         

        3)   Wash slides in 0.1x SSC at 40 °C for 5-15 minutes.

         

        4)   Wash slides in 2x SSC at 40 °C for 5-15 minutes.

         

        5)   Cool slides to room temperature.

         

        6)   Equilibrate slides in detection buffer for 5 minutes.

         

        7)   Block in blocking buffer for 20-30 minutes.

         

        8)   Incubate with 50 µl antibody or detection compound for 30-60 minutes (e.g., 5 µg/ml Streptavidin-Cy3 in blocking buffer).

         

        9)   Wash slides in 2x SSC for 5 minutes, repeat twice.

         

        10)           Counterstain with DAPI solution for 10 minutes.

         

        11)           Rinse briefly and mount in antifade mounting medium.

         

        12)           Analyze with fluorescence microscope.

         

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