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        白介素10(人類rDNA衍生)WHO參考試劑
        ??【編號(hào)】:NIBSC93/722

        ??【名稱】:白介素10(人類rDNA衍生)WHO參考試劑

        ??【規(guī)格】:個(gè)

        ??【價(jià)格】:2600元

          白介素10(人類rDNA衍生)WHO參考試劑

          編號(hào):NIBSC93/722
          英文:Interleukin-10 (Human rDNA derived) WHO Reference Reagent
          中文:白介素1受體拮抗劑
          標(biāo)準(zhǔn)類型:非世衛(wèi)組織參考材料
          規(guī)格:1個(gè) 
          描述:1. INTENDED USE
        This Standard is the primary biological standard for IL-10.
        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-10 approximately 1 microgram
        9.0 mg sodium chloride
        1.0 mg trehalose
        2.0 mg human serum albumin
        The IL-10 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. 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-10 at a 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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