copycontrol induction solution (Lucigen Corp)
86
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Lucigen Corp
copycontrol induction solution
Copycontrol Induction Solution, supplied by Lucigen Corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/copycontrol+induction+solution/1x+copycontrol+induction+solution/pm40910264-125-25-28
Average 86 stars, based on 1 article reviews
Copycontrol Induction Solution, supplied by Lucigen Corp, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/copycontrol+induction+solution/1x+copycontrol+induction+solution/pm40910264-125-25-28
Average 86 stars, based on 1 article reviews
copycontrol induction solution - by Bioz Stars,
2026-10
86/100 stars
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Plasmid Preparation:Article Title: Raiding nature's genetic toolbox for UV-C resistance by functional metagenomics. Article Snippet: .. Plasmid pCC1FOS was induced to high copy number by the addition of Article Title: Raiding nature’s genetic toolbox for UV-C resistance by functional metagenomics Article Snippet: .. Plasmid pCC1FOS was induced to high copy number by the addition of Incubation:Article Title: Raiding nature's genetic toolbox for UV-C resistance by functional metagenomics. Article Snippet: .. Plasmid pCC1FOS was induced to high copy number by the addition of Article Title: Raiding nature’s genetic toolbox for UV-C resistance by functional metagenomics Article Snippet: .. Plasmid pCC1FOS was induced to high copy number by the addition of Amplification:Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans. Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) (Kamath et al., 2003) was used to create dsRNA in vitro, which was then injected into UD87 as described previously (Chang et al., 2013; Fire et al., 1998). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: A CDC-42-regulated actin network is necessary for nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described previously ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Bacteria:Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans. Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) (Kamath et al., 2003) was used to create dsRNA in vitro, which was then injected into UD87 as described previously (Chang et al., 2013; Fire et al., 1998). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: A CDC-42-regulated actin network is necessary for nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described previously ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Purification:Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans. Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) (Kamath et al., 2003) was used to create dsRNA in vitro, which was then injected into UD87 as described previously (Chang et al., 2013; Fire et al., 1998). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: A CDC-42-regulated actin network is necessary for nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Article Title: Actin and CDC-42 contribute to nuclear migration through constricted spaces in C. elegans Article Snippet: For the cgef-1 RNAi experiments, clone X-2A03 from the Ahringer RNAi library (Source Bioscience) ( ) was used to create dsRNA in vitro , which was then injected into UD87 as described previously ( ; ). .. Fosmids used in the cgef-1 rescue experiments were from the C. elegans Fosmid Library (Source BioScience) and were amplified in bacteria using Cell Culture:Article Title: Genomic context sensitizes regulatory elements to genetic disruption Article Snippet: .. Briefly, for initial verification, TransforMax EPI300 E. coli colonies were picked into 3-5 mL LB-Kan supplemented with Article Title: Genomic context sensitizes regulatory elements to genetic disruption. Article Snippet: Assembled payloads were isolated from candidate yeast clones using the Zymo yeast miniprep I protocol (Zymo Research D2001) and transformed into TransforMax EPI300 E. coli cells by electroporation using the manufacturer’s protocol. .. Payload DNA was prepped and verified as previously described.10 Briefly, for initial verification, TransforMax EPI300 E. coli colonies were picked into 3-5 mL LB-Kan supplemented with Virus:Article Title: Genome-Wide Simplification of the AcMNPV Genome Using Synthetic Biology. Article Snippet: Large-scale genome simplification represents a fundamental goal in synthetic biology.. Baculoviruses, with their biphasic life cycle and inherent genomic plasticity, have emerged as ideal models for synthetic genome engineering.. Although modified baculovirus genomes are widely used as expression vectors for robust recombinant protein production, many genomic regions are dispensable for in vitro budded virus (BV) production. |