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You searched for "ProCHO 4"
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ProCHOTM 4 Protein-free CHO Medium, 1L
Catalog #: 04-919Q
ProCHOTM 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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ProCHOTM 4 Protein-free CHO Medium, 1L
Catalog #: BEBP12-029Q
ProCHOTM 4 Protein-free CHO Medium with 0.1% Pluronic® F-68 and phenol red, without L-Glutamin, hypoxanthine or thymidine, 1 L
ProCHOTM 4 Protein-free CHO Medium, 1L
Catalog #: BP04-919Q
ProCHOTM 4 Protein-free CHO Medium with 0.1% Pluronic® F-68, without L-Glutamin, phenol red, hypoxanthine or thymidine, 1 L
PowerFeed™ A – Chemically Defined and Protein-free Powder kit 100 L
Catalog #: BE15-044J
PowerFeed™A, CD , Protein free, Powder kit 100L
PowerFeedTM A Chemically Defined and Protein-free liquid Medium, 1 L
Catalog #: BE02-044Q
PowerFeedTM A Chemically Defined and Protein-free liquid medium, 1L
PowerFeed™ A – Chemically Defined and Protein-free Powder kit 50 L
Catalog #: BE15-044F
PowerFeed™A, CD , Protein free, Powder kit 50L
PowerFeed™ A – Chemically Defined and Protein-free basal Powder 50 L
Catalog #: VPW-095F
PowerFeed™A, CD , Protein free, Basal Powder without ferric citrate, 50L
PowerFeedTM A Chemically Defined and Protein-free Powder kit 10 L
Catalog #: BE15-044D
PowerFeedTM A Chemically Defined and Protein-free Powder, 10L
PowerFeed™ A – Chemically Defined and Protein-free basal Powder 10 L
Catalog #: VPW-095D
PowerFeed™A, CD , Protein free, Basal Powder without ferric citrate, 10L
PowerFeedTM A - Chemically Defined and Protein-free basal Powder, 100 L
Catalog #: VPW-095J
PowerFeed Chemically Defined and Protein-free basal Powder without ferric citrate, 100L
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MV-4-11 Transfection Protocol - Nucleofector™ I/II/2b Device SeriesInstructions of use for transfection of MV-4-11 cells with the Cell Line Nucleofector™ Kit L
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BE02-056Q CHO Xtreme™ Feed CD - InstructionsBE02-056Q
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SourceBook Section III - Loading and Running DNA in Agarose Gels1. DNA Loading 2. Loading Buffers 3. Optimal Voltage and Electrophoretic Times 4. Fast Running Protocols for High Resolution in MetaPhor® Agarose Gels 5. References
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SourceBook Section IV - Detection and Sizing of DNA in Agarose Gels1. Guide to Lonza Ladders and Markers 2. Detecting DNA with GelStar® and SYBR® Green Nucleic Acid Gel Stains 3. Detecting DNA with Ethidium Bromide 4. High Sensitivity Detection using the FlashGel® System 5. References
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SourceBook Section XII - Isoelectric Focusing of Proteins on Agarose Gels1. Introduction 2. Preparation of Agarose Isoelectric Focusing Gels 3. Running Agarose IEF Gels 4. Staining Proteins in Agarose IEF Gels 5. Press Blot Transfer of Proteins from Agarose IEF Gels 6. Preparative Isoelectric Focusing 7. Immunofixation/Immunoperoxidase or Autoradiography 8. Direct Tissue Isoelectric Focusing 9. Resolution Reference Guide 10. References
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SourceBook Section VI - Recovery of DNA from Agarose Gels1. Tips for Increasing DNA Recovery Efficiency from Agarose Gels 2. b-Agarose Recovery of DNA from Agarose Gels 3. Electroelution of DNA from Agarose Gels 4. Phenol/Chloroform Extraction of DNA from Agarose Gels 5. "Modified Freeze/Squeeze" Extraction of DNA from Agarose Gels 6. Ethanol Precipitation of DNA Recovered from Agarose Gels 7. References
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SourceBook Section II - Preparation of Agarose Gels1. Agarose Selection Guide 2. Agarose and Compatible Techniques 3. Agarose Types 4. Agarose Analytical Specifications 5. Suggested Agarose Concentrations & Dye Migration Information 6. Buffers for Electrophoresis 7. Dissolving Agarose 8. Casting Agarose Gels
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SourceBook Section VIII - Separation of RNA in Agarose Gels1. Introduction 2. Preparation of RNA Samples 3. Buffers for RNA Electrophoresis 4. Electrophoresis of RNA 5. Detection of RNA in Agarose Gels with GelStar® or SYBR® Green II Gel Stains 6. Detecting RNA with Ethidium Bromide 7. Northern Blotting 8. FlashGel® System for RNA Analysis 9. References
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Instructions - Limulus Amebocyte Lysate (LAL) Kinetic-QCL® (Spanish)Detailed instructions for performing the Kinetic-QCL® Kinetic Chromogenic LAL Assay in Spanish
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SourceBook Section V - In-Gel Reactions1. Overview 2. Tips for Increasing the Efficiency of In-Gel Reactions 3. Cloning in the Presence of Agarose 4. Restriction Digestion in the Presence of Agarose 5. DNA Amplification in the Presence of Agarose 6. References
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