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        白介素11(人類,rDNA衍生)WHO參考試劑
        ??【編號】:NIBSC92/788

        ??【名稱】:白介素11(人類,rDNA衍生)WHO參考試劑

        ??【規格】:個

        ??【價格】:2600元

          白介素11(人類,rDNA衍生)WHO參考試劑

          編號:NIBSC92/788
          英文:Interleukin-11 (Human, rDNA derived) WHO Reference Reagent
          標準類型:國際參考試劑
          規格:1個 
          描述:1. INTENDED USE
        This Standard is the primary biological standard for IL-11.
        2. CAUTION
        This preparation is not for administration to humans or animals in
        the human food chain.
        The preparation contains material of human origin, and either the final
        product or the source materials, from which it is derived, have been
        tested and found negative for HBsAg, anti-HIV and HCV RNA. As with
        all materials of biological origin, this preparation should be regarded as
        potentially hazardous to health. It should be used and discarded
        according to your own laboratory's safety procedures. Such safety
        procedures should include the wearing of protective gloves and
        avoiding the generation of aerosols. Care should be exercised in
        opening ampoules or vials, to avoid cuts.
        3. UNITAGE
        The assigned potency is 5000 Units of biological activity per
        ampoule.
        4. CONTENTS
        Country of origin of biological material: United Kingdom.
        Each ampoule contains a freeze dried residue comprising, under an
        atmosphere of nitrogen:
        IL-11 approximately 500 ng
        Potassium phosphate buffer
        2.0 mg trehalose
        5.0 mg human serum albumin
        The IL-11 protein was expressed in E.coli.
        5. STORAGE
        For economy of use, it is recommended that the solution be sub divided
        into several small aliquots and stored at -40ºC or below. Avoid repeated
        thawing/freezing. Unopened ampoules should be stored at -20ºC.
        Please note: because of the inherent stability of lyophilized
        material, NIBSC may ship these materials at ambient temperature.
        6. DIRECTIONS FOR OPENING
        DIN ampoules have an 'easy-open' coloured stress point, where the
        narrow ampoule stem joins the wider ampoule body. Various types of
        ampoule breaker are available commercially. To open the ampoule,
        tap the ampoule gently to collect material at the bottom (labelled) end
        and follow manufactures instructions provided with the ampoule
        breaker.
        7. USE OF MATERIAL
        No attempt should be made to weigh out any portion of the freeze-dried
        material prior to reconstitution
        Dissolve the total contents of the ampoule in 0.5ml of sterile distilled
        water. Rinse the ampoule with about 0.4ml of sterile distilled water and
        make up the total volume to 1.0ml with distilled water. This solution will
        contain IL-11 concentration of 5000 Units/ml. Use carrier protein where
        extensive dilution is required.
        8. STABILITY
        Reference materials are held at NIBSC within assured, temperaturecontrolled
        storage facilities and they should be stored on receipt as indicated on the label. It is the policy of WHO not to assign an expiry date
        to their international reference materials. Accelerated degradation studies
        have indicated that this material is suitably stable, when stored at -20ºC
        or below, for the assigned values to remain valid until the material is
        withdrawn or replaced. These studies have also shown that the material
        is suitably stable for shipment at ambient temperature without any effect
        on the assigned values. Once reconstituted, diluted or aliquoted, users
        should determine the stability of the material according to their own
        method of preparation, storage and use. Users who have data
        supporting any deterioration in the characteristics of any reference
        preparation are encouraged to contact NIBSC.
        9. REFERENCES
        This standard was produced under WHO guidelines cited in the WHO
        Technical Reports Series, No. 800, 1990, Annex 4.
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