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        Histological fixatives 组织固定剂和固定方法

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        Histological fixatives 组织固定剂和固定方法

        Fixation:

        1. Confers chemical stability on the tissue
        2. Hardens the tissue (helps further handling)
        3. Halts enzyme autolysis
        4. Halts bacterial putrefaction
        5. May enhance later staining techniques
        6. Introduces a 'consistent artefact'


        Classification:

        • Fixatives may be classed as precipitant (P) or non-precipitant (NP) according to their effect on tissue protein.
        • Primary fixatives are:
        • Acetic acid (NP)
        • Chromium trioxide (P)
        • Ethanol (P)
        • Formaldehyde (NP)
        • Mercuric chloride (P)
        • Methanol (P)
        • Osmium tetroxide (NP)
        • Picric acid (P)
        • Potassium dichromate (NP)

        Acetic alcohol - fixation time 1 minute.

        (For smears, cytospin preparations or frozen sections).

        95% methanol - 100ml

        Glacial acetic acid - 3ml.

        The sections should be washed in water before staining.

         


        Bouin's fluid - fixation time 6 hours.

        Saturated aqueous solution of picric acid - 75ml

        Formalin (~ 40% aqueous solution of formaldehyde) - 25ml

        Glacial acetic acid - 5ml

        Fixed tissue should be transferred to 70% alcohol.

         


        Carnoy's fluid - fixation time 1-3 hours.

        Ethanol - 60ml

        Chloroform - 30ml

        Glacial acetic acid - 10ml

        Fixed tissue should be processed immediately or transferred to 80% alcohol.

         


        Formol sublimate - fixation time 4-6 hours.

        Formalin (~ 40% aqueous solution of formaldehyde) - 100ml

        Mercuric chloride (saturated aqueous) - 900ml

        Fixed tissue should be transferred to 80% alcohol.

         


        Helly's fluid - fixation time 12-24 hours.

        Stock solution:-

        Potassium dichromate - 25g

        Mercuric chloride - 50g

        Sodium sulphate - 10g

        Distilled water - 1000ml

        For use:-

        Stock solution - 100ml

        Formalin (~ 40% aqueous solution of formaldehyde) - 5ml

        The fixative solution should be made up just before use. Fixed tissue must be washed for 24 hours in running tap water prior to
        processing.

         


        Neutral buffered formalin - fixation time 12-24 hours.

        Formalin (~ 40% aqueous solution of formaldehyde) - 100ml

        Sodium dihydrogen orthophosphate (monohydrate) - 4g

        Disodium hydrogen orthophosphate (anhydrous) - 6.5g

        Distilled water - 900ml

        This fixative is suitable for most histological purposes. It is to be preferred to formol-saline (a single 10% solution of formalin in
        9% aqueous NaCl) as formalin pigment is avoided. Specimens may be stored in this fluid. The solution is isotonic.

         


        Michel's fixative for immunoflourescence - fixation time 24-48 hours.

        Buffer :

        0.81g potassium citrate

        0.0625g N-ethylmaleimide - HANDLE WITH CARE!

        0.123g magnesium sulphate

        100mls distilled water

        Before use add 55g ammonium sulphate and allow to dissolve.

        Adjust pH to 7.0-7.2 with 1M KOH.

        Place tissue biopsies in fixative for 24-48 hours.  Wash tissues in buffer, three times over 10 minutes, and freeze at -70o C.

         


        Paraformaldehyde - fixation time depends on technique to follow.

        Sodium dihydrogen orthophosphate 2.26% - 41.5ml

        Sodium hydroxide 2.52% - 8.5ml

        Heat to 60-80o C in a covered container.

        Add 2g `Analar' paraformaldehyde and stir until dissolved. Filter.

         


        Zenker's fluid - fixation time 4-24 hours.

        Distilled water - 950ml

        Potassium dichromate - 25g

        Mercuric chloride - 50g

        Glacial acetic acid - 50g

        Fixed tissue should be washed overnight in running tap water before processing.

         


        REMOVAL OF FIXATION PIGMENTS

        Formalin pigment

        1. Dewax the sections, rinse in 100% alcohol, rinse in 70% alcohol, rinse in distilled water.

        2. Treat in saturated alcoholic picric acid for 30 minutes to 2 hours.

        3. Wash well in running tap water.

        4. If yellow staining of the section persists rinse in dilute lithium carbonate.

        5. Rinse in tap water.

        6. Continue with method.

         


        Mercury pigment

        1. Dewax the sections, rinse in 100% alcohol, rinse in 70% alcohol, rinse in distilled water.

        2. Treat in Lugol's iodine for 2 minutes.

        3. Decolourise in 5% sodium thiosulphate for 5 minutes.

        4. Wash well in running tap water.

        5. Continue with method.

         


        Dichromate pigment

        1. Dewax the sections, rinse in 100% alcohol, rinse in 70% alcohol, rinse in distilled water.

        2. Treat in 2% HCl in 70% alcohol 16-24 hours.

        3. Rinse in tap water.

        4. Continue with method.

        <center> <p>  </p> </center>
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