We narrowed to 809 results for: MAK;

... vast catalog of eligible AAV plasmids and we’ll make the viral vector prep you need. Or fill out our ...

...conditional auxin-inducible degron system Masato Kanemaki 92099 AAVS1_Puro_Tet3G_3xFLAG_Twin_Strep Tet-inducible...

... vast catalog of eligible AAV plasmids and we’ll make the viral vector prep you need. Or fill out our ...

...generating gRNAs makes CRISPR one of the most scalable genome editing technologies, making CRISPR perfect... Gootenberg, J. S., Abudayyeh, O. O., Slaymaker, I. M., Makarova, K. S., Essletzbichler, P., Volz, S. ...very close proximity to the region to be edited, making the PAM sequence (NGG) limiting. This PAM is abundant...Anti-CRISPR Small Precision Edits CRISPR can be used to make small, very precise edits of a handful of bases,...RNA-binding protein to stabilize pegRNAs Twin PE — two PEs make complementary edits to opposite strands Prime editing...the ability to target almost any genomic locus, makes CRISPR an ideal genome engineering system for large-scale...large-scale, forward genetic screening. CRISPR can make highly specific, permanent genetic modifications...

...order of nucleotides makes up the genetic code and provides the instructions to make every protein within...Once you have constructed a plasmid, you can easily make an endless number of copies of the plasmid using...of the known primer region with very few errors, making it an efficient and reliable sequencing method....and can only sequence short pieces of DNA. This makes it difficult to sequence an entire plasmid or genome...A,C,T, or G) is labeled with a different color, making it easy to identify the order of the DNA strand...

...engineered lentiviral vectors have many aspects that make them useful research tools in a variety of cell ...plasmids also contain a deletion in the 3’ LTR to make them self-inactivating (SIN). This deletion is transferred... long-term, constitutive expression. In order to make stable cell lines, VSV-G is often put under an inducible...Stable Cell Lines Lentiviral vectors can be used to make stable cell lines due to their integration into ... by daughter cells. Inheritance of the barcodes makes lentiviral libraries popular for lineage tracing...

...number will continue to increase. This diversity makes rAAV vectors a very useful system for preferentially...capacity for long-term gene expression. These features make them ideal for gene therapy, neuroscience research...channelrhodopsins, halorhodopsins, and other optogenetic genes makes them suitable to be packaged in the relatively small...choice for the delivery of CRISPR/Cas9 elements, making it one of the most common methods for in vivo CRISPR-based...shown higher efficiency in delivering large genes makes use of split inteins, proteins that carry out a ...

... invasive. Different activation wavelengths also make it possible to combine multiple opsins in the same...00136-4 PMID: 37933248 Gradinaru, V., Zhang, F., Ramakrishnan, C., Mattis, J., Prakash, R., Diester, I., Goshen...20621963 Mattis, J., Tye, K. M., Ferenczi, E. A., Ramakrishnan, C., O'Shea, D. J., Prakash, R., Gunaydin, L...Finkelstein, J., Paz, J. T., Stehfest, K., Fudim, R., Ramakrishnan, C., Huguenard, J. R., Hegemann, P., & Deisseroth...

...plasmid libraries, the plasmids must first be used to make virus. This pooled virus is subsequently used to...that an infected cell receives only one plasmid. To make sure that every plasmid is adequately represented...electroporation and maxiprep). If delivering as virus, make virus; this creates a pooled lentiviral CRISPR library...

...exhibited high levels of constitutive activity, making them less than ideal. DREADDs Designer Receptors... previously used in human populations in Japan, making it an attractive option for translational studies... workflows (such as laser or LED illumination), making LMOs a versatile option. Coupling brighter bioluminescent...

... gamma-retroviral vectors have many aspects that make them useful research tools in a variety of cell ... long-term, constitutive expression. In order to make stable cell lines, VSV-G is often put under an inducible...Lines Gamma-retroviral vectors are often used to make stable cell lines. Like their popular lentiviral...

...plasmids. Animals - Antibodies produced in animals make use of the animal’s immune system. The antigen of...Overview of application Collect and lyse samples to make proteins available. Tissue samples may need additional...Ready to put your new knowledge to use? Addgene now makes ready-to-use recombinant antibodies made from plasmids...

...a given gene. There are three main portions that make up a eukaryotic promoter: the core promoter, the...proteins (such as activators and structural proteins) make up the transcription complex. The most 3' portion...

...repeated throughout a specific DNA sequence. This can make it difficult at times to identify compatible restriction...site-specific recombination or a ligation step, making it an easy, cheap, and rapid cloning method. LIC...

...setting up CRISPR experiments. We will focus on making single edits using CRISPR/Cas9 in mammalian cells...gRNA design. While there are some cases where it makes sense to manually design a gRNA, in most cases gRNA...

...pouring, you should stop pouring and re-make the gel-mix. If you’re making plates without any antibiotic you...resistance gene. The following protocol will allow you to make your own LB/agar plates with your antibiotic of ...-agar powder per L of molten agar you’d like to make. The precise mass you measure out will be based ... like to pour. For example: Because we’d like to make 20 plates, and our plates can hold a maximum of ...200 mL of media total. Importantly, we’ll actually make a bit more than 200 mL (~220 mL) just in case we...small errors in measurement. You should also always make a bit more gel-ager mix than you think you’ll need...an appropriately sized bottle for autoclaving. We make 400 mL of agar in 1 L bottles and 200 mL of agar...

... such as pipetting error and sample evaporation. Make the master mix after all the samples have been added...Pro-Tip Once a validated standard curve is obtained, make a small aliquot of each standard (enough for 1 or...value of the standard starts to drift, it’s time to make a new one. When developing the assay multiple plasmids...do NOT treat your plasmid standard with DNase ** Make 6 serial dilutions, in duplicate, of your standard...quality of the sample dilution series is critical. Make sure to pipet each dilution up and down at least...standard curve and the sample dilutions. Pro-Tip Make sure that the qPCR is valid by checking to the following...you should observe differences in Ct values that make sense for your dilutions (~3.3 difference Ct for...

...you’ll need to make buffers, media, or other solutions. A key part of this task is making sure you’re weighing...weighing by looking for a weight range on the scale. Make sure that the weight of the material you’re weighing...add the material directly to the tube to weigh it. Make sure that your scoopula or spatula is clean, and...of your reagent, transfer it into your container. Make sure that any spills produced during the protocol...you have your reagents weighed out, you can begin making your solutions!...

... growth. This conditioned medium will be used to make a cell solution later in this protocol. Isolating...solution into the conditioned medium prepared above to make a new cell solution at a concentration of 5 cells...concentration: 4 × 10 5 cells/mL To seed one 96-well plate, make 10 mL of a 5 cell/mL solution. Calculate the total...0.125 µL Because this is such a small volume, first make 1 mL of a 1:100 dilution of the homogenized cell...transfer 100 times that volume, which is 12.5 µL. To make the final 5 cell/mL solution, transfer 12.5 µL of... the same focal plane. Scan the entire plate and make note of each well in which you see growth. At this...

...volume to make gels of other agarose concentrations (e.g., 2 g of agarose in 100 mL of TAE will make a 2% ...is very little difference between the two. Note: Make sure to use the same buffer as the one in the gel... Rule For each sample you want to load on a gel, make 10% more volume than needed because several microliters...For example, if you want to load 1.0 μg in 10 μL, make 1.1 μg in 11 μL. Reference Page Top Index...