nde i restriction enzyme (New England Biolabs)
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New England Biolabs
nde i restriction enzyme
Nde I Restriction Enzyme, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 4828 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nde+i+restriction+enzyme/NdeI/pmc12811641-345-9-13
Average 99 stars, based on 4828 article reviews
Nde I Restriction Enzyme, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 4828 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/nde+i+restriction+enzyme/NdeI/pmc12811641-345-9-13
Average 99 stars, based on 4828 article reviews
nde i restriction enzyme - by Bioz Stars,
2026-09
99/100 stars
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Cloning:Article Title: Maternal RNA regulates Aurora C kinase during mouse oocyte maturation in a
translation-independent fashion Article Snippet: .. Cloning and in vitro cRNA synthesis DNA linearization of Gfp -containing plasmid was carried out using Article Title: Trade-off between canonical and unusual recombination sites promotes diversity and stability of gene cassette arrays of mobile integrons Article Snippet: .. Initially, the multiple cloning site from pCR2.1 TOPO was obtained by PCR amplification with primers M13F-NdeI and M13R-NdeI (Table ) and then introduced into pLQ369 by digestion with In Vitro:Article Title: Maternal RNA regulates Aurora C kinase during mouse oocyte maturation in a
translation-independent fashion Article Snippet: .. Cloning and in vitro cRNA synthesis DNA linearization of Gfp -containing plasmid was carried out using Plasmid Preparation:Article Title: Maternal RNA regulates Aurora C kinase during mouse oocyte maturation in a
translation-independent fashion Article Snippet: .. Cloning and in vitro cRNA synthesis DNA linearization of Gfp -containing plasmid was carried out using Article Title: Experimental evolution in the cystic fibrosis chemical environment reveals early TCA cycle flux as a central regulator of Mycobacterium abscessus biofilm formation Article Snippet: Purification of PCR products was done using the Monarch PCR & DNA Cleanup Kit (New England Biolabs), and the DNA concentration was determined with a NanoDropTM One/OneC Microvolume UV–Vis Spectrophotometer (Thermo ScientificTM) in ng/μL. pSD5hsp60 vectors were extracted from E. coli DH10B cells using the Monarch Plasmid Miniprep Kit (New England Biolabs). .. Restriction enzyme digestion was performed on pSDhsp60 vector using Article Title: Mobile group I introns at nuclear rDNA position L2066 harbor sense and antisense homing endonuclease genes intervened by spliceosomal introns Article Snippet: .. The plasmid was linearized with Amplification:Article Title: The Predicted Functional Compartmentation of Rice Terpenoid Metabolism by Trans -Prenyltransferase Structural Analysis, Expression and Localization Article Snippet: Then, those entry clones were further amplified by KOD FX polymerase (Toyobo, Osaka, Japan) with corresponding primers containing the recognition site of a Nde I restriction enzyme ( ) to allow them to be cloned into pDONR221-Kz- Nde I-sGFP [ ] for the analyses of their subcellular localizations in rice protoplasts. .. The amplified PCR products were digested with Article Title: The role of IL-16 gene polymorphisms in endometriosis Article Snippet: .. In addition, the genotyping of the samples for rs11556218 was performed by digesting the 171-bp PCR product with Article Title: Trade-off between canonical and unusual recombination sites promotes diversity and stability of gene cassette arrays of mobile integrons Article Snippet: .. Initially, the multiple cloning site from pCR2.1 TOPO was obtained by PCR amplification with primers M13F-NdeI and M13R-NdeI (Table ) and then introduced into pLQ369 by digestion with Polymerase Chain Reaction:Article Title: The Predicted Functional Compartmentation of Rice Terpenoid Metabolism by Trans -Prenyltransferase Structural Analysis, Expression and Localization Article Snippet: Then, those entry clones were further amplified by KOD FX polymerase (Toyobo, Osaka, Japan) with corresponding primers containing the recognition site of a Nde I restriction enzyme ( ) to allow them to be cloned into pDONR221-Kz- Nde I-sGFP [ ] for the analyses of their subcellular localizations in rice protoplasts. .. The amplified PCR products were digested with Article Title: The role of IL-16 gene polymorphisms in endometriosis Article Snippet: .. In addition, the genotyping of the samples for rs11556218 was performed by digesting the 171-bp PCR product with Article Title: Trade-off between canonical and unusual recombination sites promotes diversity and stability of gene cassette arrays of mobile integrons Article Snippet: .. Initially, the multiple cloning site from pCR2.1 TOPO was obtained by PCR amplification with primers M13F-NdeI and M13R-NdeI (Table ) and then introduced into pLQ369 by digestion with Clone Assay:Article Title: The Predicted Functional Compartmentation of Rice Terpenoid Metabolism by Trans -Prenyltransferase Structural Analysis, Expression and Localization Article Snippet: Then, those entry clones were further amplified by KOD FX polymerase (Toyobo, Osaka, Japan) with corresponding primers containing the recognition site of a Nde I restriction enzyme ( ) to allow them to be cloned into pDONR221-Kz- Nde I-sGFP [ ] for the analyses of their subcellular localizations in rice protoplasts. .. The amplified PCR products were digested with Activity Assay:Article Title: Mobile group I introns at nuclear rDNA position L2066 harbor sense and antisense homing endonuclease genes intervened by spliceosomal introns Article Snippet: .. The plasmid was linearized with Ligation:Article Title: Trade-off between canonical and unusual recombination sites promotes diversity and stability of gene cassette arrays of mobile integrons Article Snippet: .. Initially, the multiple cloning site from pCR2.1 TOPO was obtained by PCR amplification with primers M13F-NdeI and M13R-NdeI (Table ) and then introduced into pLQ369 by digestion with |