Yeast PE LB™

  • Protocol, Manual or Handbook Protocol MSDS, Material safety data sheet MSDS CofA, Certificate of Analysis Certificate of Analysis
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  • 786-178
  • Yeast PE LB™ Kit including Zymolyase®

  • 100 preps
  • $129.00
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  • Ambient
  • Protocol, Manual or Handbook MSDS, Material safety data sheet
  • 786-179
  • Yeast PE LB™, buffer only

  • 500ml
  • $89.00
  •   Add to Cart
  • Ambient
  • Protocol, Manual or Handbook MSDS, Material safety data sheet

Yeast PE LB™ kit has been developed for extraction of biologically active, soluble proteins from yeast cells. Yeast PE LB™ is a proprietary improvement on the lyticase (Zymolyase®) based spheroplast preparation and extraction of soluble proteins from yeast cells. Yeast PE LB™ is based on organic buffering agents and utilizes a mild non-ionic detergent, chelating agent, and a proprietary combination of various salts and agents to enhance extraction and stability of proteins.

A ready-to-use Zymolyase® preparation is also provided. Depending on the required downstream application, additional agents such as reducing agents and protease inhibitors may be added into Yeast PE LB™. Yeast PE LB™ has been tested on several widely used yeast strains.

The proprietary combination of this reagent provides a simple and versatile method of yeast protein extraction. Yeast PE LB™ eliminates the need for laborious glass bead lysis of yeast cells.

This kit is suitable for processing 100 x 50µl yeast cell pellet preparations. Yeast PE LB™ buffer is also available separately for further downstream processing.

FEATURES
    • Eliminates the need for glass bead lysis.
    • Supplied as a kit, containing Zymolyase® and reagents needed for protein extraction.
    • Suitable for processing 100 x 50µl yeast cell pellet preparations.
APPLICATIONS
    • Lysis and extraction of proteins from yeast cells.
    • Isolation of spheroplasts.
    • For the isolation of biologically active proteins.
    • Suitable for most applications including enzyme and protein purifications, electrophoresis, Western blotting and 2D-gel analysis.
References

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