05-22-2000 Neuropeptide Y, Porcine

05-22-2000
  
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      Overview

      Replacement Information
      Description
      Overview

      This product has been discontinued.

      We are offering Neuropeptide Y, Human (Cat. No. 05-23-2005) as a possible alternative. Please read the alternative product documentation carefully and contact technical service if you need additional information.





      An inhibitor of Ca2+-activated K+ channels in vascular smooth muscle cells. Stimulates Na+,K+-ATPase activity in renal tubules. Strong inhibitor of both cholecystokinin- and secretin-stimulated pancreatic secretion.
      Catalogue Number05-22-2000
      Brand Family Calbiochem®
      References
      ReferencesXiong, Z., and Cheung, D.W. 1995. Pflugers Arch. 431, 110.
      Ohtomo, Y., et al. 1994. Kidney Int. 45, 1606.
      Catzeflis, C., et al. 1993. Endocrinology 132, 224.
      Moore, R.Y. 1992. Prog. Brain Res. 93, 99.
      Tatemoto, K., et al. 1982. Proc. Natl. Acad. Sci. USA 79, 5485.
      Product Information
      CAS number83589-17-7
      FormWhite to off-white lyophilized solid
      Hill FormulaC₁₉₀H₂₈₇N₅₅O₅₇
      Chemical formulaC₁₉₀H₂₈₇N₅₅O₅₇
      Applications
      Biological Information
      Purity≥95% by HPLC
      Physicochemical Information
      Peptide SequenceH-Tyr-Pro-Ser-Lys-Pro-Asp-Asn-Pro-Gly-Glu-Asp-Ala-Pro-Ala-Glu-Asp-Leu-Ala-Arg-Tyr-Tyr-Ser-Ala-Leu-Arg-His-Tyr-Ile-Asn-Leu-Ile-Thr-Arg-Gln-Arg-Tyr-NH₂
      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 Harmful
      Storage -20°C
      Protect from Moisture Protect from moisture
      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

      MSDS

      Title

      Safety Data Sheet (SDS) 

      Certificates of Analysis

      TitleLot Number
      05-22-2000

      References

      Reference overview
      Xiong, Z., and Cheung, D.W. 1995. Pflugers Arch. 431, 110.
      Ohtomo, Y., et al. 1994. Kidney Int. 45, 1606.
      Catzeflis, C., et al. 1993. Endocrinology 132, 224.
      Moore, R.Y. 1992. Prog. Brain Res. 93, 99.
      Tatemoto, K., et al. 1982. Proc. Natl. Acad. Sci. USA 79, 5485.
      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.

      Revision12-May-2008 JSW
      DescriptionAn inhibitor of Ca2+-activated K+ channels in vascular smooth muscle cells. Stimulates Na+-K+ ATPase activity in renal tubules. Strong inhibitor of both cholecystokinin- and secretin-stimulated pancreatic secretion.
      FormWhite to off-white lyophilized solid
      CAS number83589-17-7
      Chemical formulaC₁₉₀H₂₈₇N₅₅O₅₇
      Peptide SequenceH-Tyr-Pro-Ser-Lys-Pro-Asp-Asn-Pro-Gly-Glu-Asp-Ala-Pro-Ala-Glu-Asp-Leu-Ala-Arg-Tyr-Tyr-Ser-Ala-Leu-Arg-His-Tyr-Ile-Asn-Leu-Ile-Thr-Arg-Gln-Arg-Tyr-NH₂
      Purity≥95% by HPLC
      SolubilityH₂O (1 mg/ml)
      Storage -20°C
      Protect from moisture
      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 Harmful
      Merck USA index14 6485
      ReferencesXiong, Z., and Cheung, D.W. 1995. Pflugers Arch. 431, 110.
      Ohtomo, Y., et al. 1994. Kidney Int. 45, 1606.
      Catzeflis, C., et al. 1993. Endocrinology 132, 224.
      Moore, R.Y. 1992. Prog. Brain Res. 93, 99.
      Tatemoto, K., et al. 1982. Proc. Natl. Acad. Sci. USA 79, 5485.