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05-22-2000 Neuropeptide Y, Porcine

05-22-2000
  
Purchase on Sigma-Aldrich

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
Global Trade Item Number
Catalogue Number GTIN
05-22-2000 0

Documentation

Neuropeptide Y, Porcine 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 Protect from moisture
-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 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.