packaging
pkg of 10 vials (5x200µL aliquots of each component)
concentration
≥5x108 VP/ml (via p24 Assay)
application(s)
CRISPR
shipped in
dry ice
storage temp.
−70°C
1 of 4
当該品目 | PCRISPR007 | PCRISPR008 | PCRISPR001 |
|---|---|---|---|
| packaging pkg of 10 vials (5x200µL aliquots of each component) | packaging pkg of 5 vials (5x200µL aliquots ) | packaging pkg of 5 vials (5x200µL aliquots ) | packaging pkg of 10 vials (5x200µL aliquots of each component) |
| concentration ≥5x108 VP/ml (via p24 Assay) | concentration ≥5x108 VP/ml (via p24 Assay) | concentration ≥5x108 VP/ml (via p24 Assay) | concentration ≥5x108 VP/ml (via p24 Assay) |
| application(s) CRISPR | application(s) CRISPR | application(s) CRISPR | application(s) CRISPR |
| shipped in dry ice | shipped in dry ice | shipped in dry ice | shipped in dry ice |
| storage temp. −70°C | storage temp. −70°C | storage temp. −70°C | storage temp. −70°C |
Application
- Functional Genomics/Target Validation
- Focused forward genetic activation screening
- Validated positive and negative controls
- Set up and optimization of screen assay
- Creation of cell lines stably expressing KRAB-dCas9
Biochem/physiol Actions
The power of CRISPR for genome engineering, coupled with the ability to perform large-scale, whole-genome loss-of-function (LOF) screening, has allowed breakthroughs in 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. CRISPR′s Nuclease-independent applications provide equal targeting specificity. 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 complements CRISPR-KO and CRISPRa (activation) and has distinct advantages over existing loss-of-function strategies like RNAi.
Features and Benefits
- Focus on your research, and we will generate your lentivirus screening library
- Compact and ready to use CRISPRi library ~6 sgRNAs
- Optimized (F+E) gRNA scaffold (pools are gRNA-only, KRAB-dCas9 sold separately)
- Can be paired with CRISPRICON to ease optimization using validated positive control targeting RAB1A and non-targeting control for assay setup
- UCOE KRAB-dCas9 for consistent effector expression across a wide variety of cell lines
- Ease of optimization: Utilizes BFP and Puromycin as selection markers under EF1alpha promoter.
General description
The Human CRISPR inhibition (CRISPRi) library (Dolcetto) is a single compact library that inhibits over 18,000 human genes and is used for genome-wide inhibition screening using a KRAB-dCas9 effector. The library is designed to be compact and efficient to maximize screening efficiency and performance, as published by Sanson, K.R., et al. Nat Commun 9, 5416 (2018).
Custom pools for follow-up screening or 10x Genomics Compatible CRISPR pools are also available by contacting your local sales representative.
Custom pools for follow-up screening or 10x Genomics Compatible CRISPR pools are also available by contacting your local sales representative.
Other Notes
2 Subpools with a minimum concentration of 5x108 VP/mL(via p24 assay)
PCRISPR003A - Human CRISPR Inhibition Dolcetto Library Set A
PCRISPR003B - Human CRISPR Inhibition Dolcetto Library Set B
PCRISPR003A - Human CRISPR Inhibition Dolcetto Library Set A
PCRISPR003B - Human CRISPR Inhibition Dolcetto Library Set B
保管分類
10 - Combustible liquids
wgk
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
適用法令
試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。
Cartagena Act Listed
cart
PCRISPR003-1KT:
jan
Kendall R Sanson et al.
Nature communications, 9(1), 5416-5416 (2018-12-24)
The creation of genome-wide libraries for CRISPR knockout (CRISPRko), interference (CRISPRi), and activation (CRISPRa) has enabled the systematic interrogation of gene function. Here, we show that our recently-described CRISPRko library (Brunello) is more effective than previously published libraries at distinguishing
アクティブなフィルタ
ライフサイエンス、有機合成、材料科学、クロマトグラフィー、分析など、あらゆる分野の研究に経験のあるメンバーがおります。.
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