We narrowed to 42 results for: Dos;
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TypeProtocol...transforming large plasmids (>10 kb) or BACs, what can I do? Chemically competent cells are fast and easy to ...cell/DNA mixture to induce membrane permeability. To do this you will need to have access to an electroporator...
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Pipetting Protocol
TypeProtocol...box and push the end of the pipette onto the tip. Do not touch the tips with your fingers to avoid contaminating...plunger, gently lower the pipette tip into the liquid. Do not submerge the pipette itself into the liquid and... -
Colony Formation Titering Assay
TypeProtocol...regularly Do not over or under-grow your cells. Thaw a new vial of cells after 20–30 passages. Do not add...Procedure Before beginning a colony formation assay, the dose of antibiotic required to kill your target cell ...determined. Treat the target cells with a range of doses of antibiotic. Determine the minimum concentration...window) required to kill all of the cells. Use this dose for the colony formation assay. Prepare a batch ... -
Handling Plasmids from Addgene - Purifying Plasmid DNA
TypeProtocol...thicker as the proteins and DNA are denatured. Pro-Tip Do not vortex at this stage or the genomic DNA will ...4. Note: Phenol-chloroform is a hazardous waste - DO NOT pour down sink. Top Protocol: Ethanol Precipitation... -
Transfection for Recombinant Antibodies
TypeProtocol...Media 10 mL 10% Pluronic-F68 40 mL 200 mM Glutagro Do not add selective reagents Store at 4 °C until use...incubator on a shaking platform set to 120 rpm. Pro-Tip Do not use cells that are over 30 passages. Section ... -
Protocol - How to Design Primers
TypeProtocol...complementary to template strand). However, primers do not need to correspond to the template strand completely... -
Protocol - How to Create a Bacterial Glycerol Stock
TypeProtocol...scrape some of the frozen bacteria off of the top. Do not let the glycerol stock unthaw! Streak the bacteria... -
Weighing Reagents Protocol
TypeProtocol...surface. Tare the weighing boat or paper. You need to do this because you don’t want to include the weight... -
AAV ddPCR Titration
TypeProtocol...entire dilution plate with Microseal adhesive seal - do not press the film, just gently cover so nothing ...collecting drops along the side of the tube. Cap gently - do not push the cap in all the way, just ensure the ... -
Protocol - Over-Agar Antibiotic Plating
TypeProtocol...the surface). We use the micropipette tip itself to do the spreading; the tip is gently bent to create an... -
Water Bath Protocol
TypeProtocol...of the tube. This way, as items are floating, you do not need to necessarily maneuver the bottles or tubes... -
Plasmid Modification by Annealed Oligo Cloning (with Protocols)
TypeProtocol...the vector with EcoRI and SalI (see diagram ). To do this, we add 5' - AATTC and G - 3' to the top oligo... -
Video Library
TypeProtocol...Protocol Storing and Handling Addgene Plasmids What to do after you receive your plasmids from Addgene Instructions... -
Centrifugation
TypeProtocol... centrifuge and be dangerous for the user. If you do not have a balanced number of samples, you may need... -
Using a Light Microscope Protocol
TypeProtocol...images directly to a computer, but many microscopes do not and you may have to dust off your drawing skills... -
Immunocytochemistry
TypeProtocol... and a negative control sample such as cells that do not express the protein of interest....titrating your antibody to determine the optimal dose. To ensure that your antibody is both functioning... -
General Transfection
TypeProtocol...8x10 5 cells in a T75 flask in a volume of 15 mL. Do not add antibiotics to the media. Use cells that ... -
Lentivirus Production
TypeProtocol...10 5 cells in a T75 flask in 15 mL DMEM Complete. Do not add pen-strep to the media. Use cells that are... -
Affinity Purification of Recombinant Antibodies with Protein A or Protein G
TypeProtocol...sample from the reservoir to a LoBind tube. Pro-Tip Do not scrape the filter with the pipette tip. Determine... -
Antibody Validation Using the Indirect ELISA Method
TypeProtocol...purified antigen to demonstrate the expected antibody dose response....probe with an antibody against the target to show a dose response. Sharing speeds science. We believe that...standard curve . If you don’t see any color change or dose response, your antibody concentration may have been... the reaction is saturated and you don't see any dose response, your antibody concentration may have been...