separate grna expression plasmids (OriGene)
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OriGene
separate grna expression plasmids
Separate Grna Expression Plasmids, supplied by OriGene, used in various techniques. Bioz Stars score: 95/100, based on 75 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/plasmid+pcas-guide/pCas-Guide/bio_rxiv__64898__2026__05__07__723586-113-10-15
Average 95 stars, based on 75 article reviews
Separate Grna Expression Plasmids, supplied by OriGene, used in various techniques. Bioz Stars score: 95/100, based on 75 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/plasmid+pcas-guide/pCas-Guide/bio_rxiv__64898__2026__05__07__723586-113-10-15
Average 95 stars, based on 75 article reviews
separate grna expression plasmids - by Bioz Stars,
2026-10
95/100 stars
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Clone Assay:Article Title: Knockout of key receptors (PDGFRA and NRP2) in the guinea pig model blocks direct and endocytic pathways of CMV cell entry. Article Snippet: Exon- specific gRNAs were designed via the online programme (http://www.rgenome.net/) to avoid off- target sites. .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Control:Article Title: Knockout of key receptors (PDGFRA and NRP2) in the guinea pig model blocks direct and endocytic pathways of CMV cell entry. Article Snippet: Exon- specific gRNAs were designed via the online programme (http://www.rgenome.net/) to avoid off- target sites. .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Expressing:Article Title: Knockout of key receptors (PDGFRA and NRP2) in the guinea pig model blocks direct and endocytic pathways of CMV cell entry. Article Snippet: Exon- specific gRNAs were designed via the online programme (http://www.rgenome.net/) to avoid off- target sites. .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: Exon 2-specific guide RNA (gRNA) was designed via an online program ( www.rgenome.net ) to avoid off-target sites. .. DNA sequences were cloned under US6 promoter control in three separate gRNA expression plasmids (pCas-Guide-EF1a-GFP; OriGene): Article Title: Selective knockout of key CMV receptors in fetal cells blocks direct and endocytic pathways of entry in the guinea pig Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Article Title: Cytomegalovirus pentamer dependent endocytic cellular infection utilizes redundant entry receptors in the guinea pig model Article Snippet: .. DNA sequences were cloned under US6 promoter control in three Plasmid Preparation:Article Title: KDM6B safeguards mineralized tissue homeostasis from mechanical stress through epigenetic control of PIEZO1-mediated mechanotransduction in the mouse incisor Article Snippet: These gRNAs were similarly cloned into the pCas-Guide-Puro-CRISPRi vector to generate a custom Piezo1 CRISPRi kit (Origene Technologies, CW312380 ). .. The Article Title: Bispecific DNA‐Peptide Probes for Targeting Receptor Pairs on Live Cells Article Snippet: For later restriction and ligation into a pAAVS1puro-DNR vector (GE100024, OriGene) for knock-in transfection, the customized sequence was equipped with overhangs compatible with KpnI and NotI restriction sites to enable transfer by restriction ligation into the pAAVS1-puro-DNR vector (Fig. S8), which provides the pAAVS1-eGFP-MS2BP-NLS-P2A-4NE.GLRP-MS2 vector (Fig. S9). .. The stable cell line was generated using Negative Control:Article Title: KDM6B safeguards mineralized tissue homeostasis from mechanical stress through epigenetic control of PIEZO1-mediated mechanotransduction in the mouse incisor Article Snippet: These gRNAs were similarly cloned into the pCas-Guide-Puro-CRISPRi vector to generate a custom Piezo1 CRISPRi kit (Origene Technologies, CW312380 ). .. The CRISPR:Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity. Article Snippet: .. An all-in-one CRISPR/Cas9 vector with tdTomato was created by replacing the Amplification:Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity. Article Snippet: .. An all-in-one CRISPR/Cas9 vector with tdTomato was created by replacing the Polymerase Chain Reaction:Article Title: Distinct TAM subset with cross-dressing capability determines the bifurcation of tumor immunity. Article Snippet: .. An all-in-one CRISPR/Cas9 vector with tdTomato was created by replacing the Stable Transfection:Article Title: Bispecific DNA‐Peptide Probes for Targeting Receptor Pairs on Live Cells Article Snippet: For later restriction and ligation into a pAAVS1puro-DNR vector (GE100024, OriGene) for knock-in transfection, the customized sequence was equipped with overhangs compatible with KpnI and NotI restriction sites to enable transfer by restriction ligation into the pAAVS1-puro-DNR vector (Fig. S8), which provides the pAAVS1-eGFP-MS2BP-NLS-P2A-4NE.GLRP-MS2 vector (Fig. S9). .. The stable cell line was generated using Generated:Article Title: Bispecific DNA‐Peptide Probes for Targeting Receptor Pairs on Live Cells Article Snippet: For later restriction and ligation into a pAAVS1puro-DNR vector (GE100024, OriGene) for knock-in transfection, the customized sequence was equipped with overhangs compatible with KpnI and NotI restriction sites to enable transfer by restriction ligation into the pAAVS1-puro-DNR vector (Fig. S8), which provides the pAAVS1-eGFP-MS2BP-NLS-P2A-4NE.GLRP-MS2 vector (Fig. S9). .. The stable cell line was generated using Knock-In:Article Title: Bispecific DNA‐Peptide Probes for Targeting Receptor Pairs on Live Cells Article Snippet: For later restriction and ligation into a pAAVS1puro-DNR vector (GE100024, OriGene) for knock-in transfection, the customized sequence was equipped with overhangs compatible with KpnI and NotI restriction sites to enable transfer by restriction ligation into the pAAVS1-puro-DNR vector (Fig. S8), which provides the pAAVS1-eGFP-MS2BP-NLS-P2A-4NE.GLRP-MS2 vector (Fig. S9). .. The stable cell line was generated using Virus:Article Title: Bispecific DNA‐Peptide Probes for Targeting Receptor Pairs on Live Cells Article Snippet: For later restriction and ligation into a pAAVS1puro-DNR vector (GE100024, OriGene) for knock-in transfection, the customized sequence was equipped with overhangs compatible with KpnI and NotI restriction sites to enable transfer by restriction ligation into the pAAVS1-puro-DNR vector (Fig. S8), which provides the pAAVS1-eGFP-MS2BP-NLS-P2A-4NE.GLRP-MS2 vector (Fig. S9). .. The stable cell line was generated using |