We narrowed to 45 results for: IRE
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TypeProtocol...you can design a set of oligos containing your desired restriction sites and add them to your existing...overlapping oligos that once annealed can be cloned directly into the overhangs generated by restriction digest...
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Water Bath Protocol
TypeProtocol...Set up your water bath so that it will reach the desired temperature by the time you need it for your experiment...water bath to prevent evaporation and maintain the desired temperature. This also helps the water bath heat... -
Protocols for Molecular Biology, Plasmid Cloning, and Viral Preps
TypeProtocol...cells Antibody Validation Using the Indirect ELISA Method Run an indirect ELISA against a purified antigen... -
Protocol - How to Ligate Plasmid DNA
TypeProtocol... likely to ligate to itself rather than to the desired insert. If you are in this situation, it is important...Additional controls are encouraged, but may only be required for troubleshooting failed ligations. The following... -
Pipetting Protocol
TypeProtocol...maximum possible setting on the pipette, set the desired volume of the liquid on the pipette. Depending ... you can slowly release the plunger. Remove the entire pipette from the container making sure not to touch... -
What is Polymerase Chain Reaction (PCR)
TypeProtocol...to the template DNA and the Taq polymerase, PCR requires free nucleotides [dNTPs; adenine (A), cytosine... thymine (T)] in an equal molar ratio. It also requires two unique single stranded DNA oligonucleotide... -
AAV Titration by qPCR Using SYBR Green Technology
TypeProtocol...Last Update: February 13, 2019 Estimate of time required: ~3 h Workflow Timeline Plate set-up: 2 h qPCR...enough master mix for all samples). Each sample requires 15 μL of master mix. Pro-Tips Use a "Universal... -
AAV Production in HEK293 Cells
TypeProtocol...recheck the pH to prevent over or undershooting the desired pH. Allow the solution to mix for 10 min and then...proceed overnight at 4 °C if needed. Transfer the entire sample to 3 x 500 mL conical bottles and centrifuge... -
Protocol - How to Create a Bacterial Glycerol Stock
TypeProtocol...plasmid DNA, the plasmid will already be in your desired bacterial strain and you will not need to obtain... -
Personal Protective Equipment (PPE) for BSL-1 and BSL-2 Labs
TypeProtocol...wear glasses/goggles in addition to the BSL-1 requirements. Conclusion Although simple, following appropriate... -
Protocol - Over-Agar Antibiotic Plating
TypeProtocol... in LB medium. The concentration of antibiotic required for effective over-agar selection has been empirically... -
Weighing Reagents Protocol
TypeProtocol...balance and then tare it. Then add the material directly to the tube to weigh it. Make sure that your scoopula... -
Protocol - How to Perform a Diagnostic Digest
TypeProtocol...linearize a plasmid to determine the size of the entire construct or excise some or all of an insert from... -
Ligation Independent Cloning
TypeProtocol...The annealed but nicked vector product is then repaired during the replication cycle. Empty vectors for... -
Fluorescence Titering Assay
TypeProtocol...the cells in the remaining well, a cell count is required for calculating the titer. Incubate for 48–72 ... -
Molecular Biology Protocol - Restriction Digest of Plasmid DNA
TypeProtocol... ∼500 ng of DNA, while molecular cloning often requires 1 µg of DNA. The total reaction volume usually... -
General Transfection
TypeProtocol...recheck the pH to prevent over or undershooting the desired pH. Allow the solution to mix for 10 min and then... -
Protocol - Bacterial Transformation
TypeProtocol... μl of a 1:5 or 1:10 dilution rather than 1 μl directly.... -
Gibson Assembly Protocol
TypeProtocol...and yield. If there are significant amounts of undesired product, gel-purify DNA segments. Otherwise, PCR... -
Lentivirus Production
TypeProtocol...recheck the pH to prevent over or undershooting the desired pH. Allow the solution to mix for 10 min and then...