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        sigma弗氏不*佐劑

        • 更新時間:  2023-07-24
        • 產品型號:  F5506
        • 簡單描述
        • sigma弗氏不*佐劑
          Biochem/physiol Actions

          弗氏佐劑可用于制備免疫原的油包水乳液。由于抗原釋放緩慢,油包水乳液中的抗原可刺激高效長期的抗體應答。

          Other Notes

          每毫升含 0.85mL 石蠟油和 0.15mL 二縮甘露醇一油酸。
        詳細介紹

        sigma弗氏不*佐劑

        FREUND'S ADJUVANT, COMPLETE AND
        INCOMPLETE
        Product Number F 5881 AND F 5506
        Storage Temperature 2-8 °C
        Product Description
        Appearance
        F 5881 Clear amber liquid containing particulate matter
        (dried cells)
        F 5506 Clear amber liquid
        Freund's Adjuvant is one of the most commonly used
        adjuvants in research. It is used as a water-in-oil
        emulsion. It is prepared from non-metabolizable oils
        (paraffin oil and mannide monooleate). If it also
        contains killed Mycobacterium tuberculosis it is known
        as Complete Freund's Adjuvant. Without the bacteria it
        is Incomplete Freund's Adjuvant. First developed by
        Jules Freund in the 1940's, Freund's Adjuvant is
        designed to provide continuous release of antigens
        necessary for stimulating a strong, persistent immune
        response1,2,3 The main disadvantage of Freund's
        Adjuvant is that it can cause granulomas, inflammation
        at the inoculation site and lesions. The mycobacteria in
        Complete Freund's attracts macrophages and other
        cells to the injection site which enhances the immune
        response. For this reason, the Complete Freund's
        Adjuvant is used for the initial injections. To minimize
        side-effects, Incomplete Freund's Adjuvant is used for
        the boosts.
        For comparisons of different adjuvant systems, see
        references 4 and 5.
        Reagents
        Each ml of F 5881 contains 1 mg of heat-killed and
        dried Mycobacterium tuberculosis (strain H37Ra, ATTC
        25177), 0.85 ml paraffin oil and 0.15 ml of mannide
        monooleate.
        Each ml of F 5506 contains 0.85 ml of paraffin oil and
        0.15 ml of mannide monooleate.
        Precautions and Disclaimer
        Please consult the Material Safety Data Sheet for
        handling recommendations before working with this
        material.
        Storage/Stability
        Store in a cooler at 2-8 °C. Do not Freeze.
        Procedure
        1. If using Complete Freund’s Adjuvant, vortex or
        shake to resuspend the Mycobacterium.
        2. Mix antigens (preferably in saline) with an equal
        volume of the adjuvant to form an emulsion. In
        order to do this, vigorous and prolonged mixing is
        needed. There are at least three methods which
        can be used to accomplish this:
        For small volumes the emulsion can be made in a
        tube. Pipet the adjuvant in the tube first. Then,
        while vortexing, add an equal volume of the antigen
        solution. Vortex vigorously until a thick emulsion
        forms.
        For intermediate volumes, use two syringes
        connected through a luer fitting. Ideally, a 3-way
        valve should be used. Take the desired amount of
        antigen solution into a glass syringe. The volume
        should not fill more than half the syringe. Take an
        equal volume of the adjuvant into another glass
        syringe. Remove all air and connect the syringes
        through the luer fitting to the 3-way valve. Adjust
        the 3-way valve such that the connection is open
        between the two syringes. Carefully depress the
        plunger from the antigen solution first, pushing the
        antigen into the oil of the adjuvant. Alternay push
        the plungers, mixing the adjuvant and the antigen
        solution into an emulsion. Continue until the
        plungers are difficult to push.
        For large volumes, use a tissue homogenizer to
        make the emulsion. Add the adjuvant to the
        homogenizer first. Run the homogenizer for a short
        time to coat the inside with the adjuvant. Add an
        equal volume of the antigen solution and run until a
        thick emulsion forms.
        3. The resulting emulsion should be very thick and a
        drop of it should not disperse if tested by placing on
        the surface of a saline solution.
        4. Transfer the emulsion to a syringe (or remove one
        syringe from the luer fitting if using the two-syringe
        method). Remove all the air. Add an appropriay
        sized needle. The samples are now ready for
        injection.6
        sigma弗氏不*佐劑

        References
        1. Freund, J. and McDermott, K., Proc. Soc. Exp. Biol.
        Med., 49, 548-553 (1942)
        2. Freund, J., Ann. Rev. Microbiol., 1, 291 (1947)
        3. Freund, J., Adv. Tuberc. Res., 7, 130 (1956)
        4. Bennett, B. et al., J. Immuno. Meth., 153, 31-40
        (1992)
        5. Deeb, B.J. et al., J. Immuno. Meth., 152, 105-113
        (1992)
        6. Harlow, E. and Lane, D., Antibodies A Laboratory
        Manual, (Cold Spring Harbor Laboratory, 1988)

         

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