mcherry coding sequence (Addgene inc)
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mcherry coding sequence
Mcherry Coding Sequence, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mcherry+coding+sequence/mcherry+coding+sequence/pm40030016-340-5-15
Average 90 stars, based on 1 article reviews
Mcherry Coding Sequence, supplied by Addgene inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mcherry+coding+sequence/mcherry+coding+sequence/pm40030016-340-5-15
Average 90 stars, based on 1 article reviews
mcherry coding sequence - by Bioz Stars,
2026-11
90/100 stars
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Knock-Out:Article Title: A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics. Article Snippet: .. Generation of Knock-out cell lines using paired CRISPR constructs pU6-iRFP (pU6-Cas9-T2A-iRFP-2A-PuroR) construct was engineered by replacing CRISPR:Article Title: A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics. Article Snippet: .. Generation of Knock-out cell lines using paired CRISPR constructs pU6-iRFP (pU6-Cas9-T2A-iRFP-2A-PuroR) construct was engineered by replacing Construct:Article Title: A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics. Article Snippet: .. Generation of Knock-out cell lines using paired CRISPR constructs pU6-iRFP (pU6-Cas9-T2A-iRFP-2A-PuroR) construct was engineered by replacing Article Title: A NANOG‐pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics Article Snippet: .. pU6‐iRFP (pU6‐Cas9‐T2A‐iRFP‐2A‐PuroR) construct was engineered by replacing Article Title: Cas9-mediated gene-editing frequency in microalgae is doubled by harnessing the interaction between importin α and phytopathogenic NLSs. Article Snippet: All plasmids encoding Cas9 variants designed in this study were constructed using pET- NLS- Cas9- 6 × His (Addgene #62934) (50) and pET- Cas9- NLS- 6 × His (Addgene #62933) (50) as backbones with the primer sets listed (SI Appendix, Table S1) and appropriate enzymes, as described in SI Appendix, Method S6. .. To construct mCherry reporters, the Article Title: Cas9-mediated gene-editing frequency in microalgae is doubled by harnessing the interaction between importin α and phytopathogenic NLSs Article Snippet: All plasmids encoding Cas9 variants designed in this study were constructed using pET-NLS-Cas9-6 × His (Addgene #62934) ( ) and pET-Cas9-NLS-6 × His (Addgene #62933) ( ) as backbones with the primer sets listed ( SI Appendix , Table S1 ) and appropriate enzymes, as described in SI Appendix , Method S6 . .. To construct mCherry reporters, the Sequencing:Article Title: A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics. Article Snippet: .. Generation of Knock-out cell lines using paired CRISPR constructs pU6-iRFP (pU6-Cas9-T2A-iRFP-2A-PuroR) construct was engineered by replacing Article Title: Actomyosin polarisation through PLC-PKC triggers symmetry breaking of the mouse embryo. Article Snippet: .. CRY2-mCherry-PKC-KD: CRY2 domain and the Article Title: A NANOG‐pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics Article Snippet: .. pU6‐iRFP (pU6‐Cas9‐T2A‐iRFP‐2A‐PuroR) construct was engineered by replacing Article Title: Cas9-mediated gene-editing frequency in microalgae is doubled by harnessing the interaction between importin α and phytopathogenic NLSs. Article Snippet: All plasmids encoding Cas9 variants designed in this study were constructed using pET- NLS- Cas9- 6 × His (Addgene #62934) (50) and pET- Cas9- NLS- 6 × His (Addgene #62933) (50) as backbones with the primer sets listed (SI Appendix, Table S1) and appropriate enzymes, as described in SI Appendix, Method S6. .. To construct mCherry reporters, the Article Title: Deep transcriptome annotation enables the discovery and functional characterization of cryptic small proteins Article Snippet: For MiD51GFP, a LAP tag (Hein et al., 2015) was inserted between MiD51 and GFP. gBlocks were purchased from IDT. .. Human altDDIT3mCherry was cloned into pcDNA3.1 by Gibson assembly using Article Title: A New Barley Stripe Mosaic Virus Allows Large Protein Overexpression for Rapid Function Analysis Article Snippet: .. The Article Title: Cas9-mediated gene-editing frequency in microalgae is doubled by harnessing the interaction between importin α and phytopathogenic NLSs Article Snippet: All plasmids encoding Cas9 variants designed in this study were constructed using pET-NLS-Cas9-6 × His (Addgene #62934) ( ) and pET-Cas9-NLS-6 × His (Addgene #62933) ( ) as backbones with the primer sets listed ( SI Appendix , Table S1 ) and appropriate enzymes, as described in SI Appendix , Method S6 . .. To construct mCherry reporters, the Plasmid Preparation:Article Title: A NANOG-pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics. Article Snippet: .. Generation of Knock-out cell lines using paired CRISPR constructs pU6-iRFP (pU6-Cas9-T2A-iRFP-2A-PuroR) construct was engineered by replacing Article Title: Actomyosin polarisation through PLC-PKC triggers symmetry breaking of the mouse embryo. Article Snippet: .. CRY2-mCherry-PKC-KD: CRY2 domain and the Article Title: A NANOG‐pERK reciprocal regulatory circuit regulates Nanog autoregulation and ERK signaling dynamics Article Snippet: .. pU6‐iRFP (pU6‐Cas9‐T2A‐iRFP‐2A‐PuroR) construct was engineered by replacing Article Title: Cas9-mediated gene-editing frequency in microalgae is doubled by harnessing the interaction between importin α and phytopathogenic NLSs. Article Snippet: All plasmids encoding Cas9 variants designed in this study were constructed using pET- NLS- Cas9- 6 × His (Addgene #62934) (50) and pET- Cas9- NLS- 6 × His (Addgene #62933) (50) as backbones with the primer sets listed (SI Appendix, Table S1) and appropriate enzymes, as described in SI Appendix, Method S6. .. To construct mCherry reporters, the Article Title: Deep transcriptome annotation enables the discovery and functional characterization of cryptic small proteins Article Snippet: For MiD51GFP, a LAP tag (Hein et al., 2015) was inserted between MiD51 and GFP. gBlocks were purchased from IDT. .. Human altDDIT3mCherry was cloned into pcDNA3.1 by Gibson assembly using Article Title: A New Barley Stripe Mosaic Virus Allows Large Protein Overexpression for Rapid Function Analysis Article Snippet: .. The Polymerase Chain Reaction:Article Title: Actomyosin polarisation through PLC-PKC triggers symmetry breaking of the mouse embryo. Article Snippet: .. CRY2-mCherry-PKC-KD: CRY2 domain and the Clone Assay:Article Title: Deep transcriptome annotation enables the discovery and functional characterization of cryptic small proteins Article Snippet: For MiD51GFP, a LAP tag (Hein et al., 2015) was inserted between MiD51 and GFP. gBlocks were purchased from IDT. .. Human altDDIT3mCherry was cloned into pcDNA3.1 by Gibson assembly using Variant Assay:Article Title: Deep transcriptome annotation enables the discovery and functional characterization of cryptic small proteins Article Snippet: For MiD51GFP, a LAP tag (Hein et al., 2015) was inserted between MiD51 and GFP. gBlocks were purchased from IDT. .. Human altDDIT3mCherry was cloned into pcDNA3.1 by Gibson assembly using Amplification:Article Title: A New Barley Stripe Mosaic Virus Allows Large Protein Overexpression for Rapid Function Analysis Article Snippet: .. The |
