...purification methods are more straightforward and enable direct identification of molecules associated with a genomic...CRISPR-based purification, design your gRNA sequence to direct dCas9 to a specific locus, avoiding known transcription...

...TnsC, and TniQ). Type I CASTs can result in bidirectional insertions and may not be suitable for applications... I, type V-K CASTs appear to exhibit almost unidirectional insertions, but are more prone to off-target...

...gRNA-defined target sequence. DSBs are preferentially repaired in the cell by non-homologous end joining (NHEJ...present, the cell may repair a DSB using homology-directed repair (HDR) instead of NHEJ. In most experimental...

...gRNA-defined target sequence. DSBs are preferentially repaired in the cell by non-homologous end joining (NHEJ...present, the cell may repair a DSB using homology-directed repair (HDR) instead of NHEJ. In most experimental...

...that utilize Golden Gate cloning to insert the desired guide RNA sequence by digestion of the backbone...Otx2 expression in the developing mouse retina requires a unique enhancer and either Ascl1 or Neurog2 ...

... engineering TAL effector repeat arrays of any desired length: the REAL (Restriction Enzyme And Ligation...assembly process or lists of plasmid ID numbers required for FLASH assembly. Links to additional pages ...

... not exist in nature, but have been created by directed evolution of the Escherichia coli TadA, a tRNA...wider editing window, and are thus well suited to directed evolution applications. Examples of these base...

...DreO-bGHpA (50363-AAV5) Flp vectors pAAV-EF1a-mCherry-IRES-Flpo (55634-AAV1) pAAV-EF1a-Flpo (55637-AAV1) Viral...Testing AAV inventory for the entire collection! We are expanding our entire control AAV inventory to give...promoter directs ubiquitous expression. pAAV-mDlx-NLS-mRuby2 (99130-AAVrg): The Dlx element directs expression...in the last few months. You can also browse our entire AAV inventory. Our new AAVs include: EGFP-expressing...pAAV-hSyn-DIO-EGFP (50457-AAV5): The Synapsin promoter directs broad, neuronal expression. AAV pCAG-FLEX-EGFP-...112677-AAV5 and 112677-AAVrg): The EF1a promoter directs strong, ubiquitous expression. This is a Cre-dependent...

...higher than the parental vectors. pC-GoldyTALEN directs expression of TALENs from a truncated CAGs promoter...domains (DD, RR) used are obligate heterodimers that require cloning of left and right TALEN monomer proteins...

...Multiple gRNA plasmids may be used. The HDR (homology directed repair) donor plasmid with homology arms and selection...Rep. 2015 . Alternatively, cDNAs can be cloned directly into this vector and targeted to the AAVS1 genomic...

... culture. Prep size may be scaled based on the required DNA yield. Perform maxi-prep for each CRISPR/Cas9...step 6 ). Select the clones identified with the desired deletion and move to larger plate or flask for ...

...mutations in p53 and Lkb1 , as well as homology directed repair-mediated Kras G12D mutations, leading to...This plasmid also contains a Kras G12D homology directed repair donor template. #60225 - AAV:ITR-U6-sgRNA...

...vectors if you need to. Additionally, they have an IRES-Puro marker to facilitate stable cell clone selection... of dollars, but by approaching it from a new direction, we hope to do it much faster. Years of science...

...shRNA Tools for RNAi! Cre-Lox technology CAG-GFP-IRES-CRE (Plasmid #48201) This retroviral vector from...silencing mechanism. Scientists can express siRNAs to direct the cellular RNAi machinery to silence target genes...

...with the opsin or chemogenetic receptor, through an IRES or 2A sequence. In this case, the proteins are not...chemogenetic receptors used in these techniques cannot be directly visualized with fluorescence or immunohistochemistry...

... genes packaged in them and use elements such as IRES or 2A to co-express them from one promoter. Specificity...

...acceptor, contains sequence that is over 80% GC. Some IRES sequences also contain regions that are GC rich.... refined and user friendly, to own the process entirely remains a large undertaking. Priority number one... usually confirm the insert through BLAST or by direct alignment to an NCBI reference sequence or a sequence...workflow and yield sufficient data to capture the entire viral genome. The full details of that workflow...

...Two unique gRNAs, binding ~15-25 bp apart, are required for dCas9-FokI to dimerize at a given region of...

...protocol for constructing TALE repeat arrays of any desired sequence, referred to as the REAL (Restriction ...

...CRISPR Activate and Interfere technologies also indirectly modify local chromatin state. Want more information...