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addgene 43802  (Addgene inc)


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    Structured Review

    Addgene inc addgene 43802
    Addgene 43802, supplied by Addgene inc, used in various techniques. Bioz Stars score: 93/100, based on 128 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cas9/p414-TEF1p-Cas9-CYC1t+(Plasmid+%2343802)/pmc12856427-1-10-10
    Average 93 stars, based on 128 article reviews
    addgene 43802 - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Clone Assay:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Cloning:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Plasmid Preparation:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system
    Article Snippet: .. The operations are as follows: The codon-optimized Cas9 from Streptococcus pyogenes was obtained from the plasmid p414-TEF1p- Cas9-CYC1t (Addgene number: #43802) and used for expression in B . cinerea TB-31. ..

    Article Title: ROS signaling mediates aeration-dependent thermotolerance in Kluyveromyces marxianus for high-temperature xylitol production.
    Article Snippet: This study uncovers that moderate reactive oxygen species (ROS) signaling mediates aeration-dependent thermotolerance in Kluyveromyces marxianus, challenging the long-held paradigm that ROS function solely as toxic metabolic byproducts.. Through integrated transcriptomic profiling and RT-qPCR validation, 19 key transcription factors regulating this adaptive response were identified, and functional assays demonstrated that targeted knockout of GSF2 and RIM101 coupled with MED15 overexpression significantly enhances hypoxic thermotolerance.. The ERG6-overexpressing strain YZB559 yields 72.45 g/L xylitol at 45 ◦C under medium–high oxygen (MHO) condition, marking a 20% improvement over the parental strain, while the combinatorially engineered YZB639 (ΔGSF2::MED15) achieves 74.13 g/L xylitol with complete xylose consumption at 46 ◦C and 30.64 g/L ethanol under micro-oxygen conditions, representing a 23% increase in ethanol production.

    Article Title: Discovery and validation of ASG1 as a novel determinant of NaCl tolerance in the yeast Saccharomyces cerevisiae through iterative crossing
    Article Snippet: .. CRISPR-Cas9 endonuclease experiment was performed similarly as described by DiCarlo et al. ( ): SpCas9 endonuclease was firstly expressed from a low-copy CEN6/ARS4 p414 plasmid (#43802, Addgene) with clonNat selection under a strong constitutive TEF1 promoter. ..

    Construct:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Polymerase Chain Reaction:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Ligation:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Transformation Assay:

    Article Title: Development of a CRISPR/Cas12a genome editing toolbox in Kluyveromyces marxianus and its application in succinic acid biosynthesis
    Article Snippet: Primers, plasmids, strains, genes used in this study are summarized in p414-TEF1p-Cas9-CYC1t (Addgene 43802) was obtained from Addgene. .. The FnCas12a gene from Francisella novicida was codon-optimized, cloned into the p414-TEF1p-Cas9-CYC1t using a seamless cloning kit (Sangon Biotech Co., Shanghai, China), and replaced the original SpCas9 gene, resulting in the plasmid pZB214. pZB211 that containing the fragment P ScSNR52 -DR was constructed by PCR with p426-SNR52p-gRNA.CAN1.Y-SUP4t (Addgene 43803) as template using primers 5′-phosphorylation 426P-F and 426P-R following ligation and transformation. ..

    Expressing:

    Article Title: Metabolic reprogramming of abscisic acid-producing strain Botrytis cinerea TB-31 toward terpenoid biosynthesis using a CRISPR/Cas9 ribonucleoprotein system
    Article Snippet: .. The operations are as follows: The codon-optimized Cas9 from Streptococcus pyogenes was obtained from the plasmid p414-TEF1p- Cas9-CYC1t (Addgene number: #43802) and used for expression in B . cinerea TB-31. ..

    other:


    CRISPR:

    Article Title: Discovery and validation of ASG1 as a novel determinant of NaCl tolerance in the yeast Saccharomyces cerevisiae through iterative crossing
    Article Snippet: .. CRISPR-Cas9 endonuclease experiment was performed similarly as described by DiCarlo et al. ( ): SpCas9 endonuclease was firstly expressed from a low-copy CEN6/ARS4 p414 plasmid (#43802, Addgene) with clonNat selection under a strong constitutive TEF1 promoter. ..

    Selection:

    Article Title: Discovery and validation of ASG1 as a novel determinant of NaCl tolerance in the yeast Saccharomyces cerevisiae through iterative crossing
    Article Snippet: .. CRISPR-Cas9 endonuclease experiment was performed similarly as described by DiCarlo et al. ( ): SpCas9 endonuclease was firstly expressed from a low-copy CEN6/ARS4 p414 plasmid (#43802, Addgene) with clonNat selection under a strong constitutive TEF1 promoter. ..



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