178462 Apolipoprotein C-II, Human Plasma, Very Low-Density Lipoprotein

178462
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      Přehled

      Replacement Information

      Ceny a dostupnost

      Katalogové číslo DostupnostBalení ks/bal. Cena Množství
      178462-50UG
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      Dostupné omezené množství
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          Plastová ampulka 50 μg
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          Description
          OverviewNative apolipoprotein C-II from human plasma. Found primarily in VLDL and chylomicrons. Functions as a cofactor for lipoprotein lipase. Elevated serum levels of Apo C-II are common in type I, III, IV, and V hyperlipoproteinemia. Low serum concentrations of Apo C-II are indicative of nephrotic syndrome (Tangier’s Disease).
          Catalogue Number178462
          Brand Family Calbiochem®
          SynonymsApo C-II
          References
          ReferencesBrunzell, J.D. 1989. in The Metabolic Basis of Inherited Disease, 6th Edition (Scriver, G.R., ed.) p. 1165, McGraw Hill, New York.
          Le, N.A., et al. 1988. J. Lipid Res. 29, 669.
          Jackson, R.L., and Holdsworth, G. 1986. Methods Enzymol. 128, Chapter 14.
          Product Information
          FormLyophilized
          FormulationLyophilized from 10 mM NH₄HCO₃, pH 7.4.
          Quality LevelMQ100
          Applications
          Biological Information
          Purity≥95% by SDS-PAGE
          SourcePrepared from plasma that has been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.
          Physicochemical Information
          Dimensions
          Materials Information
          Toxicological Information
          Safety Information according to GHS
          Safety Information
          Product Usage Statements
          Storage and Shipping Information
          Ship Code Ambient Temperature Only
          Toxicity Standard Handling
          Storage -20°C
          Do not freeze Ok to freeze
          Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Packaging Information
          Transport Information
          Supplemental Information
          Specifications

          Documentation

          Apolipoprotein C-II, Human Plasma, Very Low-Density Lipoprotein MSDS

          Title

          Safety Data Sheet (SDS) 

          Apolipoprotein C-II, Human Plasma, Very Low-Density Lipoprotein Certificates of Analysis

          TitleLot Number
          178462

          References

          Přehled odkazů
          Brunzell, J.D. 1989. in The Metabolic Basis of Inherited Disease, 6th Edition (Scriver, G.R., ed.) p. 1165, McGraw Hill, New York.
          Le, N.A., et al. 1988. J. Lipid Res. 29, 669.
          Jackson, R.L., and Holdsworth, G. 1986. Methods Enzymol. 128, Chapter 14.
          Data Sheet

          Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

          Revision15-April-2008 RFH
          SynonymsApo C-II
          DescriptionNative apolipoprotein C-II from human plasma. Found primarily in VLDL and chylomicrons. Functions as a cofactor of lipoprotein lipase. Elevated serum levels of Apo C-II are often present in type I, III, IV and V hyperlipoproteinemia. Low serum concentrations of Apo C-II are indicative of nephrotic syndrome (Tangier disease).
          FormLyophilized
          FormulationLyophilized from 10 mM NH₄HCO₃, pH 7.4.
          SourcePrepared from plasma that has been shown by certified tests to be negative for HBsAg and for antibodies to HIV and HCV.
          Purity≥95% by SDS-PAGE
          SolubilityH₂O. Please refer to vial label for lot-specific volume prior to lyophilization.
          Storage -20°C
          Do Not Freeze Ok to freeze
          Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
          Toxicity Standard Handling
          ReferencesBrunzell, J.D. 1989. in The Metabolic Basis of Inherited Disease, 6th Edition (Scriver, G.R., ed.) p. 1165, McGraw Hill, New York.
          Le, N.A., et al. 1988. J. Lipid Res. 29, 669.
          Jackson, R.L., and Holdsworth, G. 1986. Methods Enzymol. 128, Chapter 14.