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FlashGel® DNA Marker
FlashGel® DNA Marker, 100 bp – 4 kb, 500 µL, ready-to-use marker
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FlashGel™ DNA Marker
FlashGelTM DNA Marker, 50 bp – 1.5 kb, 500 µL, ready-to-use marker
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FlashGel™ DNA Marker, 100 bp – 3 kb
FlashGelTM DNA Marker, 100 bp – 3 kb, 500 µL, ready-to-use marker
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FlashGel™ QuantLadder, 100 bp (3 ng) – 1.5 kb (30 ng)FlashGel™ QuantLadder, 250 µL, 100 bp (3 ng) - 1.5 kb (30 ng) for size and quantity estimation of DNA fragments.Catalog #: 50475Sales unit: eachCompareSave to list Save to list
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FlashGel™ DNA Starter KitFlashGel™ DNA Starter Kit, including a FlashGel™ Dock, a box of 1.2% FlashGel™ DNA Cassettes, FlashGel™ Loading Dye (5X) and FlashGel™ DNA MarkerCatalog #: 57026Sales unit: eachCompareSave to list Save to list
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ProSieve™ Color Protein Marker
ProSieveTM Color Protein Marker, 10-190 kDa, 100 µL
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ProSieve™ Color Protein Marker
ProSieveTM Color Protein Marker, 10-190 kDa, 500 µL
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FlashGel™ DNA Cassettes
FlashGelTM DNA Cassettes, 1.2% 16+1 well double-tier, 9 pack
Easily screen 32 samples
Separation: 50 bp - 4 kb
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FlashGel™ DNA Cassettes
FlashGelTM DNA Cassettes, 1.2% 12+1 well single-tier, 9 pack
Separation: 50 bp - 4 kb (up to 10 kb with lower voltage/longer run)
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Catalog #: 57023Sales unit: eachCompareSave to list Save to list -
FlashGel™ DNA Cassettes
FlashGelTM DNA Cassettes, 2.2% 16+1 well double-tier, 9 pack
Ideal for screening up to 32 samples with small DNA fragments (e.g. PCR products)
Separation: 10 bp - 1 kb
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FlashGel™ DNA Cassettes
FlashGelTM DNA Cassettes, 2.2% 12+1 well single-tier, 9 pack
Ideal for testing 12 samples with small DNA fragments (e.g. PCR products)
Separation: 10 bp - 1 kb
Catalog #: 57031Sales unit: eachCompareSave to list Save to list -
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You searched for "dna marker%3A%3A%3A%3A"
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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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Lonza SimplyLoad™ DNA Ladders - Protocol
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eBook by The Scientist and Lonza: Primary Cells in ResearchAn ebook produced in conjunction with The Scientist highlighting Primary Cells, Primary Cell Culture Process, In Vitro, and Relevant In Vitro Models.
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NK Cell Assay using 3D Bioprinted Tumor ModelsThis white paper describes an ex vivo assay for NK cell killing activity in a 3D bioprinted cervical cancer tumor model.
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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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Lonza DNA Ladders - ProtocolInstructions for proper use of Lonza DNA Ladders
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DNA Standards in Incert™ Agarose - ProtocolFor size estimation of megabase DNA separated by pulsed field gel (PFG) electrophoresis, Lonza offers 2 DNA standards in InCert Agarose Gel Plugs: Lambda DNA ladders (c1857S7) Saccharomyces cerevisiae chromosomal DNA (YPH80)
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Transfection of Primary Human HepatocytesEfficient Transfection and Sustained Long Term Functionality
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FlashGel™ Dye & Marker - ProtocolInstructions for proper use of FlashGel Dyes & Markers
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Lambda DNA Ladders in Incert® Agarose Gel Plugs - Protocol
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Webinar - Hepatocytes in the Drug Development PipelineOverview of how primary hepatocytes are used in drug development
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First siRNA Library Screening in Hard-to-Transfect HUVEC and Jurkat CellsHigh 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.
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RNA Marker 0.5-9 kb - ProtocolInstructions for proper use of RNA Marker 0.5-9 kb
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Efficient Transfection of Cancer Cell Lines Using the 4D-Nucleofector™ SystemProduct data sheet showing efficient tranfection of cancer cell lines
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3D Natural Killer Cell-mediated Cytotoxicity AssayLonza White Paper
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Superior Electrophoresis Results with Lonza Reagents and the Azure cSeries Imaging SystemsThis application note demonstrates the high-sensitivity and quality results that can be obtained combining the expertise of Lonza and Azure Biosystems for DNA and protein electrophoresis and analysis.
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Poster: Use of FlashGel® Cassettes for separations in gene editing workflowsPresented at ABRF 2020, we demonstrate here the use of FlashGel“ DNA Cassettes as tools to monitor the results of several electrophoretic separation steps that maybe involved in the CRISPR/Cas9 gene editing workflow: mismatch cleavage assays, single guide RNA (sgRNA) screening, and single stranded DNA (ssDNA) production.
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The Cell and Gene Therapies Journey from Translation to CommercializationDownload our comprehensive eBook on how to accelerate cell and gene therapy development, from translation to GMP production and commercialization.
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Automated Cell Signaling Assays Using Primary HUVECsLonza's Primary HUVECs are an excellent cell type to measure the effects of pharmacologically-important compounds on vial signaling pathways, and they provide increased data relevancy compared to cell lines.