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ExperimentShuttle peptides enable in vivo gene editing with Cas9 and Cas12a RNP in mouse airway epithelia
Experiment ConditionS10, Cas9
Assay Description: Quantitation of GFP+ cells in large and small airways following 1 delivery of GFP protein by GFP positive cells compared to DAPI stained cells.
Tissue Measured:epithelium of bronchiole
Measurement Type:Editing Efficiency
Record ID15000000278

EditorAlt-R™ S.p. Cas9 Nuclease V3
Delivery SystemS10
Delivery System SubtypeAmphiphilic peptide
Guideg-loxP2_C9
Vector

Model SpeciesMouse
Model NameGt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo

Sample Age8-10 weeks

Application Methodnasal instillation
Application Siteairway epithelium
Dosage [S10]: 40 µM; [Cas9]: 1.33 µM; [gRNA]: 2 µM
Injection Frequencyonce
Injection Ratedaily for 2 consecutive days
Injection Volume50 microliters
Days post injection7 days
Editor Formatribonucleoprotein (RNP)
Antidote Id
Antidote Descriptioncilia (α-tubulin); nuclei (DAPI)

Measured Values
Samples Size: 5
 
Replicate Result (Editing Efficiency)
Measurement Units: % of cells
Mean 8.90 
1 13.7 
2 9.8 
3 3.4 
4 9.8 
5 7.8 
  

Publication Title
Engineered amphiphilic peptides enable delivery of proteins and CRISPR-associated nucleases to airway epithelia. NCBI