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        Gonad Fixation

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        <center> <font color="#00005a"><font>Gonad Fixation</font> </font><br /> - From R. Francis -</center>

        A. Methanol
        Methanol fixation is quick, easy, and gives satisfactory nuclear morphology after DAPI staining. However, methanol-fixed gonads break easily and are more difficult to mount than formaldehyde-fixed gonads. Fix dissected gonads in 3 ml of cold (-20¡) methanol for 5 min. Using a pasteur pipette, transfer to a glass conical glass tube, add 2ml PBTw and spin 1 min in a clinical benchtop centrifuge at setting 2. Remove the supernatant and wash 2x in several ml PBTw. Fixed gonads can be stored in methanol at -20¡ for a week or two before use. 

        B. Formaldehyde
        Gives better nuclear morphology and less shrinkage than MeOH fixation.  Fix in 2 - 3 ml of 3% Formaldehyde/0.1 M K2HPO4  (pH 7.2) for 1 hr. After fixation,  transfer to a 5 ml glass conical tube (The more narrow the bottom is, the better), add a few mls of PBTw and spin 1 min in clinical benchtop centrifuge at setting 3.  Remove super, wash 1x in PBT, and then post-fix in 2 ml of 100% Methanol (from -20 C stock) for 5 min.  Fill tube with PBT, spin, remove super ( I usually leave about 200 ul), and transfer the worms into a small (6 mm X 35 mm) glass culture tube (siliconized, Kimax brand) .  Alternatively, fixed gonads can be stored in MeOH at -20C for a few days.  Storing in methanol for longer periods is possible, but subsequent staining seems of a lower quality. 

        C. Methanol / Formadehyde
        This fixation protocol is fast and gives better DAPI-nuclear morphology than methanol by itself. To make the fixative, mix 10 mls of 16% formaldehyde, 3.3 mls of 0.1 M K2 HPO4 (pH7.2), and 40 ml methanol. This solution is stored at -20¡ and is used as described for methanol (but increase fixation time to 10 min). 

        D. Glutaraldehyde / Formaldehyde
        Glutaraldehyde / formaldehyde fixation works well for germline RNA in situs: gonads remain intact through extensive protease treaments (40 ug/ml Proteinase K for 30 min) that would destroy gonads fixed in formaldehyde alone. This fixation has also been used with good results with some antibodies. Mix 10 ml of 16% formaldehyde, 0.53 ml of 25% glutaraldehyde (EM grade), and 43 ml of 0.1 M K2 HPO4 (pH 7.2). Store the fixative in 5-10 ml aliquotes at -20¡C. Fix gonads for 2 hr at rom temperature with a 5 min MeOH post-fix (as described above for formadehyde).

        Materials
        PBS: Sambrook et al. (Molecular Cloning ).
        PBTw: PBS containing 0.1% Tween 20.
        3% formaldehyde / 0.1 M K2 HPO4 (pH7.2): Prepare from sealed ampoules of 16% EM grade formaldehyde (EM Sciences). Freeze any excess. This solution can also be made from paraformaldehyde powder.
        Methanol: 100% stock kept at -20¡C. 

         

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