We narrowed to 997 results for: lars

...also use a nucleotide-based molecular insert (inosine) instead of a regular nucleotide for broader pairing...

...undergo homology-directed repair (HDR), a distinct cellular DNA repair pathway. Accomplishing this usually... iPSC-based models of neurodegenerative and neurovascular diseases. He worked on the described project...

... plate, do NOT dig into the agar. Another very popular technique is to draw in discontinuous lines. Start...30 °C instead of 37 °C. This is often true for large unstable plasmids, which sometimes recombine at ...

...both groups on a western blot and look for the molecular weight shifts indicative of tau phosphorylation...against a protein standard (P) to check for tau molecular weight shifts. A negative control is a sample...

... pH7.5-8.0, 50mM NaCL, 1mM EDTA) and mixed in equimolar concentrations. We recommend mixing 2μg each ...μl). Mix the annealed oligos with cut vector in molar ratios (vector:insert) between 4:3 and 1:6 in a ...

... like... Cloning Methods Empty Backbone Guide Molecular Biology Protocols Overview Ligation Independent...Transform Mix your treated vector and insert at a molar ratio of 1:2 or 1:3, using between 20 and 50 ng ...

...success in numerous fields such as microbiology, molecular biology or cell biology. Learn some of the key...samples. This is a commonly used technique for molecular cloning, such as PCR- or restriction enzyme-based...

... looking at a process-oriented team serving a particular function. Project team A Project Team is assembled...an excuse. Every psych test I’ve ever taken has declared me an introvert, and I identify as one.  But some...

[email protected]. These deposits are considered large deposits and are exceptions to our standard workflow...your plasmid is designed to allow you to produce large amounts of your insert in E. coli, then this is ...

...and reagents from other vendors should produce similar outcomes when using these protocols. However, please...replication use a HEK293 line stably expressing the SV40 large T antigen. For antibody-expressing plasmids containing...

... a Liquid Bacterial Culture Introduction Many molecular biology techniques require highly purified and... of bacteria to grow (low copy plasmids require larger cultures). Centrifuge the culture to pellet the...

...will need to use a phosphatase to prevent re-circularization of the recipient plasmid. You should treat ...Additionally, if your final product is going to be very large (>10kb) you might want to use electro-competent ...

...from academic viral vector cores. Our titers were similar to those reported by these institutions. This protocol...Concentration of Addgene plasmid #59462 : 1.07 μg/μL Molecular Weight: 6208 bp x 650 dalton/bp or (g/mole)/bp...

...and reagents from other vendors should produce similar outcomes when using these protocols. However, please...plate washer (optional) Scale Microsoft Excel or similar software Reagents Purified antigen Purified recombinant...

...empirically, and that the cell population be monitored regularly for transgene expression. This protocol has been...over-confluent, trypsinize the cells and expand them to larger culture dishes, being sure not to cross contaminate...

...37°C, 5% CO 2 overnight. Although cells should regularly be passaged in DMEM + 10% FBS with penicillin/...limited to the implied warranties of fitness for a particular purpose, non-infringement, typicality, safety...

...and additions describing CRISPR’s ability to make large genome edits using transposases or the Cascade-Cas3...

... to me: Selective Endogenous eNcapsidation for cellular Delivery (SEND). On the fourth day of CRISPR, ...

...Enhanced prime editing systems by manipulating cellular determinants of editing outcomes🎵 On the 5th ...

... technologies are going? What is the next hot molecular biology technology? Have you deposited your plasmids...