Thiolutin

Description

Thiolutin is used to inhibit RNA synthesis in bacteria and fungi and to study transcriptional regulation, redox biology, and stress response pathways. It is frequently applied in cell-based experiments to rapidly suppress RNA production and assess changes in gene expression over defined time intervals. Thiolutin is a sulfur-containing antibiotic originally isolated from Streptomyces species and is known for its metal-binding and redox-active properties.

Mechanism: Thiolutin interferes with RNA polymerase activity, leading to inhibition of RNA synthesis. Its activity has been associated with redox-dependent interactions and metal chelation, which can influence transcriptional machinery and other cellular processes. Through this disruption of transcription, thiolutin enables controlled examination of RNA-dependent pathways and downstream regulatory responses.

 

Key Features and Advantages

  • Transcriptional Inhibition: Suppresses RNA synthesis, supporting studies of gene expression dynamics.

  • Redox-Active Compound: Exhibits redox-dependent behavior that can influence cellular stress responses.

  • Metal Chelation Properties: Capable of interacting with metal ions, which may contribute to its biological activity.

  • Broad Biological Activity: Active in both bacterial and fungal systems, expanding experimental utility.

  • Tool for Temporal Gene Expression Studies: Enables short-term inhibition of transcription to examine regulatory cascades.

 

Common Applications and Usage Notes

  • Gene Expression Analysis: Used to halt transcription prior to RNA extraction for stability or decay studies.

  • Transcriptional Stress Experiments: Applied to evaluate cellular responses to acute inhibition of RNA synthesis.

  • Fungal and Bacterial Growth Inhibition Studies: Incorporated into culture systems to assess susceptibility and transcriptional control.

  • Redox Biology Investigations: Utilized in experiments exploring redox-sensitive signaling pathways.

 

Practical Tips

  • Metal Interaction Consideration: Because thiolutin can chelate metal ions, media composition and metal supplementation may influence activity and reproducibility.

  • Rapid Onset of Transcriptional Block: RNA synthesis inhibition can occur quickly after exposure. Time course design should account for rapid transcriptional changes.

  • Redox Sensitivity: Experimental outcomes may vary under strongly oxidizing or reducing conditions. Maintain consistent redox environments when comparing results.

  • Storage/Handling: Upon receipt, store this product at -20°C.

 

Thiolutin

View Sizes & Pricing

Catalog Number:
T-235-2
CAS Number:
87-11-6
$328.00

Availability:
2-3 Weeks
Shipping:
Shipping calculated at checkout

    Description

    Thiolutin is used to inhibit RNA synthesis in bacteria and fungi and to study transcriptional regulation, redox biology, and stress response pathways. It is frequently applied in cell-based experiments to rapidly suppress RNA production and assess changes in gene expression over defined time intervals. Thiolutin is a sulfur-containing antibiotic originally isolated from Streptomyces species and is known for its metal-binding and redox-active properties.

    Mechanism: Thiolutin interferes with RNA polymerase activity, leading to inhibition of RNA synthesis. Its activity has been associated with redox-dependent interactions and metal chelation, which can influence transcriptional machinery and other cellular processes. Through this disruption of transcription, thiolutin enables controlled examination of RNA-dependent pathways and downstream regulatory responses.

     

    Key Features and Advantages

    • Transcriptional Inhibition: Suppresses RNA synthesis, supporting studies of gene expression dynamics.

    • Redox-Active Compound: Exhibits redox-dependent behavior that can influence cellular stress responses.

    • Metal Chelation Properties: Capable of interacting with metal ions, which may contribute to its biological activity.

    • Broad Biological Activity: Active in both bacterial and fungal systems, expanding experimental utility.

    • Tool for Temporal Gene Expression Studies: Enables short-term inhibition of transcription to examine regulatory cascades.

     

    Common Applications and Usage Notes

    • Gene Expression Analysis: Used to halt transcription prior to RNA extraction for stability or decay studies.

    • Transcriptional Stress Experiments: Applied to evaluate cellular responses to acute inhibition of RNA synthesis.

    • Fungal and Bacterial Growth Inhibition Studies: Incorporated into culture systems to assess susceptibility and transcriptional control.

    • Redox Biology Investigations: Utilized in experiments exploring redox-sensitive signaling pathways.

     

    Practical Tips

    • Metal Interaction Consideration: Because thiolutin can chelate metal ions, media composition and metal supplementation may influence activity and reproducibility.

    • Rapid Onset of Transcriptional Block: RNA synthesis inhibition can occur quickly after exposure. Time course design should account for rapid transcriptional changes.

    • Redox Sensitivity: Experimental outcomes may vary under strongly oxidizing or reducing conditions. Maintain consistent redox environments when comparing results.

    • Storage/Handling: Upon receipt, store this product at -20°C.

     

    Product Specifications

    Catalog ID: T-235
    CAS #: 87-11-6
    Formula: C8H8N2O2S2
    MW: 228.29 g/mol
    Storage/handling: Store at -20°C.
    UN number: 2811
    item class: 6.1
    group number: II
    PubChem Chemical ID: 6870

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