... none, need Cas9 plasmid Bullock and Port 51026 U6-BbsI-crRNA dU6 BbsI Transfection none, need Cas9 plasmid...type Cas enzymes. To use a nickase mutant, you will need two gRNAs that target opposite strands of your DNA...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...Injection or in vitro transcription Virmilion none, need Cas9 plasmid Bullock and Port 49411 pCFD4-U6:1_U6...Injection or in vitro transcription Virmilion none, need Cas9 plasmid Bullock and Port 49330 pAc-sgRNA-Cas9...45946 pU6-BbsI-chiRNA dU6 BbsI Transfection none, need Cas9 plasmid O'Connor-Giles, Harrison, Wildonger...

...none, need Cas9 plasmid Joung 46170 PU6::klp-12_sgRNA cU6 PCR (see paper) Transfection none, need Cas9 ...Transfection none, need Cas9 plasmid Boxem 47941 pMB60 T7 BsaI In vitro transcription none, need Cas9 plasmid...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...-scaffold SP6 AflII In vitro transcription none, need Cas9 plasmid Sternberg 177783 L4440_BioBrick-sgRNA...BioBrick-sgRNA T7 BbsI, BsaI Ingestion by C. elegans none, need Cas9 plasmid Ristow Do you have suggestions for ...

...expect to produce our guaranteed titer, and will give you the option to proceed with your order, or not...plasmids with sequence from the 5′ to the 3′ ITR exceeding 4.7 kb Transfer plasmids with a cargo that may...not, without a guaranteed titer. Any titer expectations communicated by email will supersede the general...our viral production does not yield the titer guaranteed here or by email, Addgene will contact you to...that email within 10 business days in order to proceed with any adjustments to the original order. Turnaround...days of ordering. We will give you the option to proceed with your order, or not, with a longer turnaround...this email within 10 business days in order to proceed with any adjustments to the original order. Experimental...

...spacers into the PX330 vector backbone? There is no need to add the NGG PAM sequence. Because the 'NGG' of...the PAM is used to select your genomic target, you need to make sure the NGG immediately follows your target... order is: 5'-CACCGN...N-3' 3'-CN...NCAAA-5' You need to add the CACC and AAAC cloning overhang. When ...starts with a 'G', you naturally have one and do not need to add an additional 'G'. Where are double strand...be sufficient to generate off-target DSBs; there needs to be extensive homology of the protospacer followed...your cells. If you want to use double nickase, you need to have four spacers co-expressed and using PX335...the double nickase system, with PX335 vector, you need to find two guides for each cleavage site, but this...

...process may need to be optimized for individual assays. Clear cell debris by sedimentation. Proceed with IP..., an antimicrobial agent, can block some amines needed for conjugation reactions and should be removed...chosen. Signal Amplification The amount of signal needed from a specific antibody can vary depending on ...category, including an outline of the basic steps needed for each application, important controls, and any...samples to make proteins available. Tissue samples may need additional processing steps, such as sonication....signal levels. In ChIPseq, an input control will need to be collected before immunoprecipitation. Antibody...from. Then consider the following questions: Do you need polyclonal or monoclonal antibodies? Will you be...

...type Cas enzymes. To use a nickase mutant, you will need two gRNAs that target opposite strands of your DNA...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target...’re using does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...pCRISPR BsaI E. coli, S. pneumoniae Kanamycin none, need Cas9 plasmid Marraffini 42876 pCas9 BsaI E. coli...pgRNA-bacteria BBa_J23119 SpeI + HindIII Ampicillin none, need Cas9 plasmid Qi Do you have suggestions for other...

...type Cas enzymes. To use a nickase mutant, you will need two gRNAs that target opposite strands of your DNA...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target...’re using does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...handle_RPR1t pRPR1 HindIII S. cerevisiae LEU2 none, need Cas9 plasmid Lu Do you have suggestions for other...

...human transmembrane transporters. Feedback Please send your feedback to the Resolute Partnership using... NeuroMab Collection Plasmids Pooled Libraries Feedback Solute carrier proteins (SLCs) are the largest...using their RESOLUTE repository feedback form . If you have further questions or comments you can also contact...

...type Cas enzymes. To use a nickase mutant, you will need two gRNAs that target opposite strands of your DNA...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target...’re using does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target...into the search bar. When using CRISPR, you will need to express both a Cas protein and a target-specific...

...type Cas enzymes. To use a nickase mutant, you will need two gRNAs that target opposite strands of your DNA...you choose does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target...’re using does not also express a gRNA, you will need to use a separate gRNA expression plasmid to target... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...

...requirements for a CRISPR knockout assay are simple. You’ll need a Cas enzyme and a gRNA specific to the gene of ...Cas9-gRNA complex binds a putative DNA target, the seed sequence (8–10 bases at the 3′ end of the gRNA targeting...) will begin to anneal to the target DNA. If the seed and target DNA sequences match, the gRNA will continue...Mismatches between the target sequence in the 3′ seed sequence inhibit target cleavage, while mismatches...NHEJ directly ligates the break ends without the need for a homologous template. Both NHEJ and HDR have... the depositing lab. After amplification, you’ll need to use next-generation sequencing (NGS) to verify...matches that of the original library. Next, you’ll need to generate lentivirus containing the entire library...

...necessary to customize an existing reagent to suit your needs. Genetic Manipulation Application Cas9 gRNA Additional...Select Expression System To use CRISPR, you will need both Cas9 and a gRNA expressed in your target cells...efficient on-target cleavage. The gRNA target sequence needs to match the target locus, but it is also critical... method of delivery and the cell type. Before proceeding with your experiment, it may be necessary to ...

...transcription none, need Cas9 plasmid Chen and Wente 42250 DR274 T7 BsaI In vitro transcription none, need Cas9 plasmid... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...

...multiple orders would need to be placed through our website. Every order will need to be completed independently...Projects and how you can provide us with input and feedback on this service. DNA Service Details Amount 2 ...

...the tet-off transactivator (tTA) with a positive feedback loop for amplified tTA expression. 1 Gradinaru...plasmids and we’ll make the viral vector prep you need. Or fill out our form to let us know what you would...

...affordable prices. While our repository serves the needs of many researchers, scientists sometimes require... our current in-stock capabilities. To meet that need, our Packaged on Request service lets scientists...Troubleshooting If your answer isn’t in the Help Center or you need more assistance with troubleshooting, we want to...

...modifications in endogenous loci with unprecedented speed and specificity. Figure 2: An overview of CRISPR...a DSB at the target genomic locus. Repair will proceed through NHEJ or HDR depending on the experimental... model system or biological topic, and you don’t need to be an expert to see results! Getting Started ...

...designed based on the target site sequence (20bp) and need to be followed on the 3' end by a 3bp NGG PAM sequence...designed based on the target site sequence (30bp) and need to be followed on the 3' end by a 3bp NGG PAM sequence... based on the target site sequence (21-22bp) and need to be followed on the 3' end by NGRRT or NGRRN PAM...

...or RNA ends up when it's expressed, you’ll likely need to tag it with something that makes it easy to see...just isn’t enough to get all the information you need. If you want to dissect an individual protein’s ...structure using X-Ray crystallography, you’ll likely need to purify it. Luckily, many proteins can be functionally...

... or cloning method. When using CRISPR, you will need to express both a Cas protein and a target-specific...Simple-gRNA backbone T7 BsaI In vitro transcription none, need Cas9 plasmid Chen Do you have suggestions for other...