We narrowed to 939 results for: TIM
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TypeProtocol... of Solution II and invert the tube carefully 5 times to mix the contents. The contents will become clear...Solution III to each tube. Mix by inverting several times. A white precipitate will be formed which contains... 0.1 mM EDTA). Pro-Tip DNA resuspension can take time, it is a good idea to let it sit for several hours...
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Personal Protective Equipment (PPE) for BSL-1 and BSL-2 Labs
TypeProtocol...feet. Pro-Tip If they are able, sometimes scientists work for a long time while standing. Wear comfortable... -
Protocol - How to Streak a Plate
TypeProtocol...it through a flame, just be sure to allow enough time for the loop to cool before touching it to the bacteria...often true for large unstable plasmids, which sometimes recombine at 37 °C. Be sure to check this before... -
Protocol - How to Purify DNA from an Agarose Gel
TypeProtocol...will want to use long-wavelength UV for as short a time as possible to get the bands cut out. Once you have...the gel at a lower voltage for a longer period of time; b) using a wider gel comb; or c) loading less DNA... -
Weighing Reagents Protocol
TypeProtocol...weigh out 100 g three times, placing the sucrose in your container after each time. Place the weighing ... -
Ligation Independent Cloning
TypeProtocol...Independent Cloning (LIC) obviates the need for the time-consuming ligation step of traditional cloning methods...sterile water (instead of TE buffer) to ensure optimal salt concentrations in subsequent reactions. Step... -
Centrifugation
TypeProtocol...place, and the control panel where you can set the time and speed needed for your experiment. Procedure ...Adjust the centrifuge settings according to speed and time (and temperature, if applicable) listed in your ... -
Fluorescence Titering Assay
TypeProtocol... institution’s biosafety regulations. Workflow Timeline Day 0: Seed 293T cells Day 1: Transduce cells ...with multiple integration events leading to underestimation of the true titer. Calculate the transduction... -
Gibson Assembly Protocol
TypeProtocol...can work fine in an assembly if you want to save time. Working on ice, combine segments in the Gibson ...rate when assembling more than five fragments at a time. Resources and References New England Biolabs (NEB... -
Plasmid Cloning by PCR (with Protocols)
TypeProtocol... making a copy of a piece of DNA and at the same time adding restriction sites to the ends of that piece...both function in the same buffer, as this will save time later. In our example, we will use EcoRI and NotI... -
DNA Quantification
TypeProtocol... the absorbance of a liquid you can accurately estimate the concentration of a substance in that liquid... -
Protocol - How to Design Primers
TypeProtocol...on a nucleotide when adding a nucleotide one at a time. The main property of primers is that they must ... -
Plasmid Modification by Annealed Oligo Cloning (with Protocols)
TypeProtocol...Transformation Summary Oligo overlap cloning can be used anytime you need to add a short stretch of DNA to a plasmid... -
Protocol - How to Perform Sequence Analysis
TypeProtocol...manually call the correct base at the position. Sometimes an “N” is the result of an erroneous insertion... -
Protocol - How to Perform a Diagnostic Digest
TypeProtocol...Although this is never an ideal cloning strategy, sometimes it cannot be avoided. If you do have to do so,... -
Video Library
TypeProtocol...offer some tips and tricks to reduce transformation time and increase efficiency Bacterial Transformation... -
Plasmid Cloning by Restriction Enzyme Digest (with Protocols)
TypeProtocol...can function in the same buffer, it will save you time in future steps. Experimental Procedure Digest your... -
Pouring LB Agar Plates
TypeProtocol...antibiotic throughout the agar. Open one plate at a time next to the flame and begin pouring. Measure your... -
Coomassie Purity Stain of Recombinant Antibodies
TypeProtocol...in science. Last Update: June 14, 2023 Workflow Timeline Day 1: Run SDS-PAGE and stain gel Day 1 or later...