lr clonase reaction kit (Thermo Fisher)
Thermo Fisher is a verified supplier 
Thermo Fisher manufactures this product 
90
Structured Review
Thermo Fisher
lr clonase reaction kit
Lr Clonase Reaction Kit, supplied by Thermo Fisher, 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/lr+clonase+reaction+kit/gateway+lr+clonase+ii+enzyme+mix/10__1038_slash_s44318___024___00356___2-373-26-30
Average 90 stars, based on 1 article reviews
Lr Clonase Reaction Kit, supplied by Thermo Fisher, 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/lr+clonase+reaction+kit/gateway+lr+clonase+ii+enzyme+mix/10__1038_slash_s44318___024___00356___2-373-26-30
Average 90 stars, based on 1 article reviews
lr clonase reaction kit - by Bioz Stars,
2026-09
90/100 stars
Images
Related Articles
Amplification:Article Title: The Natural Antisense Transcript <i>DONE40</i> Derived from the lncRNA <i>ENOD40</i> Locus Interacts with SET Domain Protein ASHR3 During Inception of Symbiosis in <i>Arachis hypogaea</i> Article Snippet: .. Amplified fragments were cloned into pENTR/D-TOPOR (Life Technologies) and then into binary vectors pK7GWIWG2D(II) (Karimi et al. 2002) by gateway technology through the Article Title: The Natural Antisense Transcript <i>DONE40</i> Derived from the lncRNA <i>ENOD40</i> Locus Interacts with SET Domain Protein ASHR3 During Inception of Symbiosis in <i>Arachis hypogaea</i> Article Snippet: .. Amplified fragments were cloned into pENTR/D-TOPOR (Life Technologies) and then into binary vectors pK7GWF2 (Karimi et al. 2002) by gateway technology through the Clone Assay:Article Title: The Natural Antisense Transcript <i>DONE40</i> Derived from the lncRNA <i>ENOD40</i> Locus Interacts with SET Domain Protein ASHR3 During Inception of Symbiosis in <i>Arachis hypogaea</i> Article Snippet: .. Amplified fragments were cloned into pENTR/D-TOPOR (Life Technologies) and then into binary vectors pK7GWIWG2D(II) (Karimi et al. 2002) by gateway technology through the Article Title: Sestrin2 drives ER-phagy in response to protein misfolding Article Snippet: The mKeima-LDHB plasmid was a gift from Stefano Santaguida. mKeima-COX8 was purchased from Addgene (Plasmid #131626). .. The plasmids mKeima-FAM134B and mKeima-FAM134C were cloned into the pDONR223 vector (Invitrogen) using the BP Article Title: The Natural Antisense Transcript <i>DONE40</i> Derived from the lncRNA <i>ENOD40</i> Locus Interacts with SET Domain Protein ASHR3 During Inception of Symbiosis in <i>Arachis hypogaea</i> Article Snippet: .. Amplified fragments were cloned into pENTR/D-TOPOR (Life Technologies) and then into binary vectors pK7GWF2 (Karimi et al. 2002) by gateway technology through the Article Title: Two FAM134B isoforms differentially regulate ER dynamics during myogenesis Article Snippet: cDNAs were cloned into lentiviral vectors using GATEWAY (Thermo Fisher Scientific) or In-Fusion (Takara Bio) systems. .. For the GATEWAY cloning the cDNAs were cloned into the pDONR223 vector using the BP Article Title: Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER‐phagy, and Collagen quality control Article Snippet: .. cDNAs were cloned into pDONR223 vector using the BP Article Title: Phosphorylation of FAM134C by CK2 controls starvation-induced ER-phagy Article Snippet: Tamoxifen (Sigma-Aldrich, #H6278) was used at 1 μM for 72 hours. .. To generate HA- and Myc-FAM134s plasmids, FAM134s and FAM134C mutants were cloned into pDONR223 vector (Invitrogen) using the BP Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy Article Snippet: .. Plasmids are presented in Supplementary Table . cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy. Article Snippet: .. Plasmids are presented in Supplementary Table 1. cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a Plasmid Preparation:Article Title: Sestrin2 drives ER-phagy in response to protein misfolding Article Snippet: The mKeima-LDHB plasmid was a gift from Stefano Santaguida. mKeima-COX8 was purchased from Addgene (Plasmid #131626). .. The plasmids mKeima-FAM134B and mKeima-FAM134C were cloned into the pDONR223 vector (Invitrogen) using the BP Article Title: Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER‐phagy, and Collagen quality control Article Snippet: .. cDNAs were cloned into pDONR223 vector using the BP Article Title: Phosphorylation of FAM134C by CK2 controls starvation-induced ER-phagy Article Snippet: Tamoxifen (Sigma-Aldrich, #H6278) was used at 1 μM for 72 hours. .. To generate HA- and Myc-FAM134s plasmids, FAM134s and FAM134C mutants were cloned into pDONR223 vector (Invitrogen) using the BP Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy Article Snippet: .. Plasmids are presented in Supplementary Table . cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy. Article Snippet: .. Plasmids are presented in Supplementary Table 1. cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a Cloning:Article Title: Two FAM134B isoforms differentially regulate ER dynamics during myogenesis Article Snippet: cDNAs were cloned into lentiviral vectors using GATEWAY (Thermo Fisher Scientific) or In-Fusion (Takara Bio) systems. .. For the GATEWAY cloning the cDNAs were cloned into the pDONR223 vector using the BP Generated:Article Title: Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER‐phagy, and Collagen quality control Article Snippet: .. cDNAs were cloned into pDONR223 vector using the BP Polymerase Chain Reaction:Article Title: Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER‐phagy, and Collagen quality control Article Snippet: .. cDNAs were cloned into pDONR223 vector using the BP Mutagenesis:Article Title: Role of FAM134 paralogues in endoplasmic reticulum remodeling, ER‐phagy, and Collagen quality control Article Snippet: .. cDNAs were cloned into pDONR223 vector using the BP Affinity Purification:Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy Article Snippet: .. Plasmids are presented in Supplementary Table . cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a Article Title: Heteromeric clusters of ubiquitinated ER-shaping proteins drive ER-phagy. Article Snippet: .. Plasmids are presented in Supplementary Table 1. cDNAs were cloned into the pDONR223 vector using a BP Clonase Reaction kit (Invitrogen, 11789100) and further recombined into the Gateway destination vectors pcDNA5-FRT/TO-N-mCherry-EGFP, pcDNA3.1-N-HA, pHAGE-GFP, pcDNA3.1-N-Flag, pcDNA3.1-C-Flag, pcDNA3.1-N-SBP-Flag, pGEX6-GST, and the biomolecular complementation affinity purification system vectors pDEST-V1-ORF, pDEST-V2-ORF, pDEST-ORF-V1 and pDEST-ORF-V2 using a |