PCRISPR006
Human CRISPR Poison Exon Knockout Library
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A propos de cet article
NACRES:
NE.02
UNSPSC Code:
41105904
packaging
pkg of 5 vials (5x200µL aliquots )
concentration
≥5x108 VP/ml (via p24 Assay)
application(s)
CRISPR
shipped in
dry ice
storage temp.
−70°C
General description
The human, paired guide Poison (pgPoison) library targets 3` splice sites with paired guide RNAs for alternative exon removal (pgRNAs), induce skipping of "poison" cassette exons and corresponding upstream constitutive exons in ultraconserved regions. This compact library (targets 963 exons) allows direct comparison between loss of a constitutive coding exon (knockout) with loss of a poison exon.
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.
Application
- Functional Genomics/Target Validation
- Dual-gRNA
- Poison exon
- Internal controls included
Biochem/physiol Actions
In traditional CRISPR KO screens, Cas9 introduces double-strand breaks at locations specified by a gRNA. In this library, a CRISPR-Cas9-based method is used by expressing two sgRNAs to manipulate isoforms independent of gene inactivation. This approach enables rapid suppression of exon recognition in polyclonal settings to identify functional roles for individual exons.
Features and Benefits
- Focus on your research, and we will generate your lentivirus screening library
- Use CRISPR nucleases to knockout protein-coding genes to assess their function.
- Built-in enrichment and depletion controls allow researchers to gauge the success of their pooled screening experiments confidently.
- Dual-Guide Vector System (pools are gRNA-only, Cas9 sold separately) See products: LVCAS9BST or LVCAS9NEO.
- Ease of optimization: Utilizes BFP and Puromycin as selection markers under EF1alpha promoter.
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Cet article | |||
|---|---|---|---|
| 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) |
| shipped in dry ice | shipped in dry ice | shipped in dry ice | shipped in dry ice |
| packaging pkg of 5 vials (5x200µL aliquots ) | packaging pkg of 5 vials (5x200µL aliquots ) | packaging pkg of 5 vials (5x200µL aliquots ) | packaging pkg of 5 vials (5x200µL aliquots ) |
| storage temp. −70°C | storage temp. −70°C | storage temp. −70°C | storage temp. −70°C |
| application(s) CRISPR | application(s) CRISPR | application(s) CRISPR | application(s) CRISPR |
Classe de stockage
10 - Combustible liquids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
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James D Thomas et al.
Nature genetics, 52(1), 84-94 (2020-01-09)
While RNA-seq has enabled comprehensive quantification of alternative splicing, no correspondingly high-throughput assay exists for functionally interrogating individual isoforms. We describe pgFARM (paired guide RNAs for alternative exon removal), a CRISPR-Cas9-based method to manipulate isoforms independent of gene inactivation. This
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| PCRISPR006-1EA | 04065266925289 |