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CRISPRICON

Sigma-Aldrich

Human CRISPRi Control and Effector Kit

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About This Item

Code UNSPSC :
12352200
Nomenclature NACRES :
NE.02

Conditionnement

pkg of 12 vials (4x50μL aliquots for each of the 3 kit components)

Application(s)

CRISPR

Conditions d'expédition

dry ice

Température de stockage

−70°C

Description générale

The control kit includes validated positive control targeting RAB1A and non-targeting control for assay set-up and a UCOE KRAB-dCas9 for consistent effector expression across a wide variety of cell lines. The kit is ideal for setting up the screen assay and optimization before using the CRISPRi library pools.

Application

  • Set up and optimization of screen assay
  • Functional Genomics/Target Validation
  • Creation of cell lines stably expressing KRAB-dCas9
  • Validated Positive and negative controls

Caractéristiques et avantages

  • Ease of optimization: Validated positive control targeting RAB1A and non-targeting control for assay set up
  • Best in Class UCSF gRNA selection algorithm and optimized (F+E) gRNA scaffold
  • UCOE KRAB-dCas9 for consistent effector expression across a wide variety of cell lines
  • Libraries provided at high functional titer, based on FACs or CFU analysis
  • Use puromycin and or BFP as selection markers

Composants

2 Controls and 1 Effector Construct with a minimum concentration of 5x105 TU/mL(via FACS or CFU assay)

CRISPRIE: KRAB-dCas9 - Blasticidin CRISPRi Construct Lentiviral Transduction Particles
CRISPRI01: CRISPRi RAB1A Puromycin Control Transduction Particles
CRISPRI06: CRISPRi Nontargeting Control Puromycin Transduction Particles

For more information about screening with CRISPRi/a please Click Here.

Principe

The power of CRISPR for genome engineering, coupled with the ability to perform large-scale, whole genome, loss-of-function (LOF) screening, has allowed for new breakthroughs identifying gene pathways in drug resistance and disease. CRISPR is most commonly used to create double-stranded breaks that often result in loss of gene function (CRISPR-KO). However, the full extent of CRISPR′s utility extends beyond just targeted cutting of DNA. Nuclease-independent applications of CRISPR provide equal targeting specificity but instead of cutting, CRISPRi allows for targeted interference of gene function by delivering transcriptional repressor domains to a specific target sequence using modified dCas9 + gRNA complexes. Gene knockdown is complementary to CRISPR-KO and CRISPRa (activation) and has distinct advantages over existing loss-of-function strategies like RNAi. We partnered with University of California San Francisco to provide the best-in-class CRISPRi screening tools available.

Code de la classe de stockage

12 - Non Combustible Liquids


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