PowerFeed® Chemically Defined and Protein-free basal Powder without ferric citrate, 100L
Pro293TMa Serum-free Medium, chemically defined for adherent cells, without L-glutamine or phenol red with 0.1% Pluronic® F-68, 1 L
Pro293sTM Serum-free Medium, chemically defined, for suspension cells, without L-glutamine, phenol red, galactose or Pluronic® F-68, 1 L
PowerCHO® 2 CD, with HEPES, Pluronic® F-68, without L-glutamine, phenol red, hypoxanthine or thymidine, 10 L bag
PowerCHO® 2 Serum-free Medium 20 L bag, chemically defined, with HEPES, Pluronic® F-68, without L-Glutamine, phenol red, hypoxanthine or thymidine.
PowerCHO® 1 Basal Powder with HEPES, Pluronic® F-68, without L-glutamine, phenol red, hypoxanthine or thymidine, 50L
PowerCHO® 2, chemically defined Basal Powder, 500 L
PowerCHO® 2 Powder kit 100 L, with HEPES, Pluronic® F-68, without L-Glutamine, Phenol red, hypoxanthine or thymidine
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ProSieve™ Protein Marker - Instructions for Conjugating AP and HRP to S-Tag50547 ProSieve Protein Marker
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ProSieve™ Unstained Protein Marker - ProtocolInstructions for proper use of ProSieve™ Unstained Protein Markers
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ProSieve™ Unstained Protein Marker II - ProtocolInstructions for proper use of ProSieve™ Unstained Protein Markers
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ProSieve™ Color Protein Marker - ProtocolInstructions for proper use of ProSieve™ Color Protein Markers
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ProSieve™ QuadColor™ Protein Marker - ProtocolInstructions for proper use of ProSieve™ QuadColor™ Protein Marker
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Protein Electrophoresis VWRVWR Cobranded Version
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Protein Electrophoresis
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Overview Lonza DNA Markers and LaddersSelect the best DNA Marker for your application
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Agaroses for Protein SeparationOverview of Agaroses for Protein separation
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SourceBook Section XIII - Protein Separation in Agarose Gels1. Introduction 2. Buffers for Protein Separation in Agarose 3. Casting Agarose Gels for Protein Separation 4. Preparation and Loading of Protein Samples 5. Optimal Voltage and Electrophoretic Times 6. Detection of Proteins in Agarose Gels 7. Gel Drying and Preservation 8. Processing Agarose Gels Following Electrophoresis 9. Recovering Proteins from Agarose Gels 10. References