text.skipToContent text.skipToNavigation
Need help? Please contact us
  1. Home
  2. ProCHO 4%3A%3A%3A%3Arelevance

You searched for "ProCHO 4%3A%3A%3A%3Arelevance"

118 Products found
Too many choices? Use the filter option on the left to narrow your product listing.
  • 1(current)
  • 2
  • 3

You searched for "ProCHO 4%3A%3A%3A%3Arelevance"

1,084 Documents found
  • Synthego-Lonza Genome Editing of Resting T cells
    Case Study on Genome Editing of Resting T cells
  • The Cell and Gene Therapies Journey from Translation to Commercialization
    Download our comprehensive eBook on how to accelerate cell and gene therapy development, from translation to GMP production and commercialization.
  • Molt-4 Transfection Protocol - 4D-Nucleofector™ X-Unit
    Instructions of use for transfection of Molt-4 cells with the SF Cell Line 4D-Nucleofector™ X Kit
  • BE02-056Q CHO Xtreme™ Feed CD - Instructions
    BE02-056Q
  • MOLT-4 Transfection Protocol - Nucleofector™ I/II/2b Device Series
    Instructions of use for transfection of MOLT-4 cells with the Cell Line Nucleofector™ Kit L
  • NB-4 Transfection Protocol - Nucleofector™ I/II/2b Device Series
    Instructions of use for transfection of NB-4 cells (DSMZ) with the Cell Line Nucleofector™ Kit V
  • First siRNA Library Screening in Hard-to-Transfect HUVEC and Jurkat Cells
    High throughput transfection of siRNA libraries has become a valuable tool in target identifi cation and validation. However, such screenings have so far been constrained to mostly easy-totransfect adherent cell lines. Lonza’s 96-well Shuttle® System, based on the well-established Amaxa® Nucleofector® Technology, extends these approaches to primary and diffi cult-to-transfect cells.
  • Transfection of Primary Human Hepatocytes
    Efficient Transfection and Sustained Long Term Functionality
  • MV-4-11 Transfection Protocol - Nucleofector™ I/II/2b Device Series
    Instructions of use for transfection of MV-4-11 cells with the Cell Line Nucleofector™ Kit L
  • Webinar - Hepatocytes in the Drug Development Pipeline
    Overview of how primary hepatocytes are used in drug development
  • Efficient Transfection of Cancer Cell Lines Using the 4D-Nucleofector™ System
    Product data sheet showing efficient tranfection of cancer cell lines
  • SourceBook Section II - Preparation of Agarose Gels
    1. 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
  • SourceBook Section III - Loading and Running DNA in Agarose Gels
    1. DNA Loading 2. Loading Buffers 3. Optimal Voltage and Electrophoretic Times 4. Fast Running Protocols for High Resolution in MetaPhor® Agarose Gels 5. References
  • SourceBook Section VI - Recovery of DNA from Agarose Gels
    1. 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
  • SourceBook Section XII - Isoelectric Focusing of Proteins on Agarose Gels
    1. 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
  • SourceBook Section IV - Detection and Sizing of DNA in Agarose Gels
    1. 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
  • Instructions - Limulus Amebocyte Lysate (LAL) Kinetic-QCL® (Spanish)
    Detailed instructions for performing the Kinetic-QCL® Kinetic Chromogenic LAL Assay in Spanish
  • SourceBook Section VIII - Separation of RNA in Agarose Gels
    1. 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
  • SourceBook Section V - In-Gel Reactions
    1. 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
  • Troubleshooting Guide - PyroGene™ Recombinant Factor C Assay Procedure (Spanish)
    This is a step-by-step guide depicting how to perform the PyroGene™ Recombinant Factor C assay.
  • 1
  • 2(current)
  • 3