Cryopreserved ampule of Rat Neonatal Retinal Cells containing ≥200,000 cells
ProSieveTM ProTrackTM Dual Color Protein Loading Buffer (4X), 5 mL
Discontinuation notification: Based on our product lifecycle management review to maintain high service levels across our portfolios, this product has been discontinued end of August 2024.
ProCHO® 5 Protein-free CHO Medium Powder kit with HEPES and 0.1% Pluronic® F-68, without L-Glutamine, phenol red, hypoxanthine or thymidine, 500 L (NAO)
ProCHO® 5 protein free CHO medium, with HEPES and 0.1% Pluronic® F-68, without L-Glutamine, phenol red, hypoxanthine or thymidine, 1 L (NAO)
UltraDOMATM Protein-free Medium, Chemically defined, Hybridoma medium, with L-Glutamine, 500 mL
ProCHO® 4 Protein-free CHO Medium with 0.1% Pluronic® F-68, without L-Glutamin, phenol red, hypoxanthine or thymidine, 1 L.
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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™ Color Protein Marker - ProtocolInstructions for proper use of ProSieve™ Color 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™ QuadColor™ Protein Marker - ProtocolInstructions for proper use of ProSieve™ QuadColor™ Protein Marker
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Protein Electrophoresis
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Protein Electrophoresis FisherFisher CoBranded Version
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Protein Electrophoresis VWRVWR Cobranded Version
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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
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SourceBook Section I - Frequently Asked Questions1. Nucleic Acid FAQs 2. Protein Analysis FAQs