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539160 Proteasome Inhibitor I - Calbiochem

Overview

Replacement Information

Key Specifications Table

Empirical Formula
C₃₂H₅₀N₄O₈

Products

Catalog NumberPackaging Qty/Pack
539160-1MG Plastic ampoule 1 mg
539160-5MG Plastic ampoule 5 mg
Description
OverviewA cell-permeable, reversible inhibitor of the chymotrypsin-like activity of the multicatalytic proteinase complex (MCP; 20S proteasome) in HT4 cells. Causes the accumulation of ubiquitinated proteins in neuronal cells. Prevents the activation of NF-κB in response to TNF-α and Okadaic Acid (Cat. No. 495604) through inhibition of IκB-α degradation. A 50 mM (5 mg/162 µl) solution of Proteasome Inhibitor I (Cat. No. 539161) in DMSO is also available.
Catalogue Number539160
Brand Family Calbiochem®
SynonymsPSI
References
ReferencesGriscavage, J.M., et al. 1996. Proc. Natl. Acad. Sci. USA 93, 3308.
Mori, S., et al. 1995. J. Biol. Chem. 270, 29447.
Figueiredo-Pereira, M.E., et al. 1994. J. Neurochem. 63, 1578.
Traenckner, E.B., et al. 1994. EMBO J. 13, 5433.
Product Information
ATP CompetitiveN
FormWhite solid
Hill FormulaC₃₂H₅₀N₄O₈
Chemical formulaC₃₂H₅₀N₄O₈
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetChymotrypsin-like activity of the multicatalytic proteinase complex (MCP; 20S proteasome) in HT4 cells
Purity≥90% by HPLC
Physicochemical Information
Cell permeableY
Peptide SequenceZ-Ile-Glu(OtBu)-Ala-Leu-CHO
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). DMSO stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalog Number GTIN
539160-1MG 04055977269420
539160-5MG 04055977269437

Documentation

Proteasome Inhibitor I - Calbiochem SDS

Title

Safety Data Sheet (SDS) 

Proteasome Inhibitor I - Calbiochem Certificates of Analysis

TitleLot Number
539160

References

Reference overview
Griscavage, J.M., et al. 1996. Proc. Natl. Acad. Sci. USA 93, 3308.
Mori, S., et al. 1995. J. Biol. Chem. 270, 29447.
Figueiredo-Pereira, M.E., et al. 1994. J. Neurochem. 63, 1578.
Traenckner, E.B., et al. 1994. EMBO J. 13, 5433.

Brochure

Title
Proteasomes Technical Bulletin

Citations

Title
  • Chung, S., et al. 2005. Journal of Biological Chemistry 280, 38445.
  • 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.

    Revision04-September-2008 RFH
    SynonymsPSI
    DescriptionCell-permeable inhibitor of the chymotrypsin-like activity of the multicatalytic proteinase complex (MCP; 20S proteasome) in HT4 cells. Causes the accumulation of ubiquitinylated proteins in neuronal cells. Prevents NF-κB activation in response to TNFα and okadaic acid through inhibition of IκB-α degradation, thereby interfering with induction of iNOS in macrophages.
    FormWhite solid
    Chemical formulaC₃₂H₅₀N₄O₈
    Peptide SequenceZ-Ile-Glu(OtBu)-Ala-Leu-CHO
    Structure formulaStructure formula
    Purity≥90% by HPLC
    SolubilityDMSO (30 mg/ml), ethanol (30 mg/ml), or methanol
    Storage -20°C
    Do Not Freeze Ok to freeze
    Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). DMSO stock solutions are stable for up to 3 months at -20°C.
    Toxicity Standard Handling
    ReferencesGriscavage, J.M., et al. 1996. Proc. Natl. Acad. Sci. USA 93, 3308.
    Mori, S., et al. 1995. J. Biol. Chem. 270, 29447.
    Figueiredo-Pereira, M.E., et al. 1994. J. Neurochem. 63, 1578.
    Traenckner, E.B., et al. 1994. EMBO J. 13, 5433.
    Citation
  • Chung, S., et al. 2005. Journal of Biological Chemistry 280, 38445.