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Promega Webinars

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Welcome to the Promega Webinar Series, an ongoing communication designed to keep you informed. Learn about basic concepts, tips and techniques to help your research, or understand how products were designed and how to implement in your lab. All presentations will be given by Promega scientists and you will have an opportunity to interact with our Technical Service Scientist directly during live events via chat. The webinars are free though we do ask that you register for the events. Registration allows us to send you the URL for the webinar.

Tracking Cellular Protein Localization and Movement in Cells with a Flexible Fluorescent Labeling Technology

Proteomics

Tuesday, January 13, 2015

Chad Zimprich, B.S.

This webinar will demonstrate how the HaloTag(R) Technology is uniquely suited to protein imaging analysis from simple cellular localization experiments to highly complex trafficking studies.

It's All in the Details (or Small RNA): Simplified and Improved miRNA Purification from Tissue

MDx

Tuesday, January 27, 2015

Douglas Horejsh, Ph.D.

This webinar will discuss the growing field of miRNA research, the roles miRNA play in cells and a new solution for miRNA purification that simplifies purification without the use of any organic pre-processing.

Did you miss one of our webinars? Simply select the appropriate link below and view the recorded webinar. It will not be interactive, but you will see the chat questions the original attendees asked. For additional information on the products discussed in the webinar, explore our links to videos and other resources.

If there is an area you would like to see covered, you can request a topic of your choice.

If you are experiencing issues opening the webinar recordings, please be sure that you have the latest Adobe Flash Player installed.

To NanoDrop® or Not to NanoDrop®: Choosing the Most Appropriate Method for Nucleic Acid Quantitation

Genomics

Tuesday, November 12, 2013

Douglas Wieczorek, Ph.D.

Success or failure in DNA/RNA analysis applications often comes down to whether or not the appropriate amount of input nucleic acid is used, but nucleic acid quantitation methods reveal different information about a sample. This webinar will review absorbance, fluorescent nucleic acid-binding dyes and qPCR quantitation methods and present the advantages and disadvantages of each method. With this information, you'll be able to choose the appropriate quantitation method based on your sample type and downstream application.

Overcoming Key Challenges of Protein Mass Spectrometry Sample Preparation with ProteaseMAX™ Surfactant

Proteomics

Tuesday, October 15, 2013

Dr. Sergei Saveliev

Surfactants such as SDS and Triton X-100 are commonly used during mass spec protein sample preparation, but these compounds are incompatible with reverse phase chromatography and mass spec and must be removed before use. This webinar will cover an easy-to-use mass spec-compatible surfactant that does not require removal prior to analysis. We will demonstrate its use and advantages for in-gel protein digestion, re-solubilization of protein pallets and other key mass spec protein sample preparation steps.

Improving Genetic Analysis: From FFPE Tissue DNA Extraction to MSI Analysis

MDx

Tuesday, September 24, 2013

Rebecca Gorshe

Many molecular genetic analyses start with DNA extracted from FFPE samples, but extraction of amplifiable DNA from these samples is difficult. This webinar will discuss methods to improve molecular genetic analysis starting with FFPE samples. Read additional information below.

Tools for Cell Metabolism: Bioluminescent NAD(P)/NAD(P)H-Glo™ Assays

Cell-Based Assays

Tuesday, September 10, 2013

Jolanta Vidugiriene, Ph.D.

Measuring nicotinamide adenine dinucleotides in cells and tissues can be challenging but important to understanding cellular energy metabolism especially in cancer. In this webinar we will discuss the challenges and introduce three new bioluminescent assays for rapid and sensitive measurement of redox defining co-factors NAD(P)/NAD(P)H.

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