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资源简介：
CRISPR-associated protein
应用场景：
创建时间：
2023-11-08
相关数据集
Guide RNA engineering enables efficient CRISPR editing with a miniature Syntrophomonas palmitatica Cas12f1 nuclease
To confirm the tolerance of SpaCas12f1, mismatched assay was performed for NGS.
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CRISPR RNA-seq from HepG2 (ENCSR194SPW)
Control CRISPR gRNA against no target in HepG2 cells followed by RNA-seq. (NT-BGHcLV07-B) For data usage terms and conditions, please refer to http://www.genome.gov/27528022 and http://www.genome.gov
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Frequency of INDEL formation in mice using gRNA synthesized from pU6T7 expression vectors.
Frequency of INDEL formation in mice using gRNA synthesized from pU6T7 expression vectors.
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Table_1_Naïve Primary Mouse CD8+ T Cells Retain In Vivo Immune Responsiveness After Electroporation-Based CRISPR/Cas9 Genetic Engineering.xlsx
CRISPR/Cas9 technology has revolutionized genetic engineering of primary cells. Although its use is gaining momentum in studies on CD8+ T cell biology, it remains elusive to what extent CRISPR/Cas9 af
NIAID Data Ecosystem50
File S2.zip
Annotated sequence files in .ape format (comparable with Genbank) of knock-ins generated by CRISPR/Cas9-mediated genome editing. Unmodified genomic sequence is also provided.
Figshare2023-03-14 更新20
