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        白介素2可溶性受體(人類,rDNA衍生)
        ??【編號】:NIBSC97/600

        ??【名稱】:白介素2可溶性受體(人類,rDNA衍生)

        ??【規格】:個

        ??【價格】:2200元

          白介素2可溶性受體(人類,rDNA衍生)

          編號:NIBSC97/600
          英文:Interleukin-2 Soluble Receptor (human, rDNA derived)
          標準類型: 非WHO參考資料
          規格:1個 
          描述:1. INTENDED USE
        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 1000 units of immunological 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-2sr approximately 30 - 100 ng
        9.0 mg sodium chloride
        1.0 mg trehalose
        2.0 mg human serum albumin
        The IL-2sr protein was expressed in CHO cells.
        NOTE: Due to the variation in estimates provided by contributors to an
        international collaborative study of the mass of IL-2sr contained within the
        ampoules, a unitage has been applied to the contents and a range
        provided for the mass content. It is strongly recommended that all
        immunoassays are calibrated in this unitage.
        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-2 sr at a concentration of 1000 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. An arbitrary unitage was assigned to this
        preparation at the time of production without confirmation of long term
        stability. Evidence from similar materials prepared by an equivalent
        process indicates that long term stability is likely to be maintained and 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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