We narrowed to 810 results for: mal
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TypeProtocol...General Transfection Introduce plasmid DNA to mammalian cells Lentivirus Production Produce lentivirus...adeno-associated virus from a preparation produced in mammalian cells Watch the Video! AAV Titration by qPCR Using...to Video Transfection Introduce plasmid DNA to mammalian cells to produce antibodies Antibody Purification...
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General Transfection
TypeProtocol...Use this protocol to transfect mammalian cells with your plasmid of interest....protocol describes a general method for transfecting mammalian cells using linear polyethylenimine. Transfections...are below passage 20 for viral production. The optimal mass DNA:mass PEI ratio will need to be empirically... -
Using a Light Microscope Protocol
TypeProtocol...These tools allow you to observe specimens much smaller than you would be able to with your naked eye, ...advantage of the physical properties of light to detect small objects. Two of the most important properties of...needed, you can also use the fine focus knob (the smaller of the focus knobs) to make minor adjustments to... -
Sequencing Primers
TypeGuide...GATGAAGCCCTGAAAGACGCGCAG (Waugh lab) 3' end of maltose binding protein, forward primer mCherry-F CCCCGTAATGCAGAAGAAGA... -
Plasmid Cloning by Restriction Enzyme Digest (with Protocols)
TypeProtocol...). You might need to express YGOI in cultured mammalian cells. The problem is that the only version of...Using subcloning, you can easily move YGOI into a mammalian expression vector. Design (Choosing enzymes) Many...purpose. Congratulations, you now have YGOI in a mammalian expression vector and can begin your studies. ... -
Virus Protocol - Generating Stable Cell Lines
TypeProtocol...transfection. Some lentiviral vectors deliver mammalian antibiotic resistance (e.g., puromycin, blasticidin...cycles. Procedure Before beginning, determine the optimal dose of selective reagent for your target cell ...important to do regular media changes and maintain optimal growth conditions for the surviving cells. Even... -
AAV Titration by qPCR Using SYBR Green Technology
TypeProtocol...internal passive reference (typically ROX dye), to normalize non-PCR–related fluorescence fluctuations and ... a validated standard curve is obtained, make a small aliquot of each standard (enough for 1 or 2 plates...acceptable) Baseline removal: all samples will have some small amount of background signal that is most evident... -
Isolating a Monoclonal Cell Population by Limiting Dilution
TypeProtocol...medium with increased serum concentrations, may be optimal for different cell types. Before starting this ...because the buildup of waste products could be suboptimal for cell growth. This conditioned medium will...10 5 cells/mL) = 0.125 µL Because this is such a small volume, first make 1 mL of a 1:100 dilution of the... -
AAV ddPCR Titration
TypeProtocol...risk of contaminating reagents we recommend making small aliquots of master mixes, primers, and probes prior...302411100 Droplet Digital PCR System, Bio-Rad, DX200 Thermal Cycler, Bio-Rad, T100 PCR Plate Sealer, Bio-Rad...plate has been sealed, proceed to thermocycling. Thermal Cycling Run the following PCR parameters. Cycling... -
Weighing Reagents Protocol
TypeProtocol...accuracy as these types of scales display more decimal places. Pro-Tip If you’re weighing out an amount...amount of reagent that will be resuspended in a small volume (e.g. 0.02 g to resuspend in 1 mL), you may... -
Protocol - How to Inoculate a Bacterial Culture
TypeProtocol...time (approximately 18-30 hr). On the other hand, smaller plasmids can be present in large numbers, 50 or...may help to increase the density of the culture. Normally cultures shake at 150 - 250 rpm, increase this... -
Ligation Independent Cloning
TypeProtocol...sterile water (instead of TE buffer) to ensure optimal salt concentrations in subsequent reactions. Step...per annealing reaction. This should be done in a small volume with no additional water (<5 μl). It is advisable... -
Handling Plasmids from Addgene - Purifying Plasmid DNA
TypeProtocol...the bacteria back into suspension, but within a smaller volume of buffer that is compatible with the next... genomic DNA to precipitate, while leaving the smaller plasmids free in solution. Pellet the proteins ... -
Pouring LB Agar Plates
TypeProtocol...~220 mL) just in case we spill anything or have small errors in measurement. You should also always make...-mix slightly. Even so, you should always use thermally insulated gloves when removing anything from the... -
Protocol - How to Design Primers
TypeProtocol... Short primers are mainly used for amplifying a small, simple fragment of DNA. On the other hand, a long... -
Protocol - How to Create a Bacterial Glycerol Stock
TypeProtocol...plasmid DNA prep the following day. Tips and FAQ The optimal concentration of long-term glycerol storage is ... -
Protocol - How to Streak a Plate
TypeProtocol...toothpicks or wire loop Bunsen burner (or other small flame source) Incubator Marker Reagents LB agar ... -
Protocol - How to Purify DNA from an Agarose Gel
TypeProtocol...higher percentage agarose gel will help resolve smaller bands from each other, and a lower percentage gel... -
Protocol - How to Perform a Diagnostic Digest
TypeProtocol...-8 pieces such that all (or most) fragments are small enough to be accurately sized on a gel and also ... -
Centrifugation
TypeProtocol...height. They often spin at similar speeds to their smaller cousins, but can hold much larger containers. Ultracentrifuges...