methyltransferase (New England Biolabs)
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95
Structured Review
New England Biolabs
methyltransferase
Methyltransferase, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 227 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dam+methyltransferase/dam+Methyltransferase/pmc13112749-355-33-34
Average 95 stars, based on 227 article reviews
Methyltransferase, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 95/100, based on 227 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/dam+methyltransferase/dam+Methyltransferase/pmc13112749-355-33-34
Average 95 stars, based on 227 article reviews
methyltransferase - by Bioz Stars,
2026-10
95/100 stars
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Concentration Assay:Article Title: The yeast genome is globally accessible in living cells. Article Snippet: .. Incubation:Article Title: The yeast genome is globally accessible in living cells. Article Snippet: .. Article Title: Nucleosome dynamics render heterochromatin accessible in living human cells Article Snippet: .. Article Title: Nucleosome dynamics render heterochromatin accessible in living human cells Article Snippet: .. Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table ) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table ), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis. Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table S1) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table S1), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Methylation:Article Title: Centromeres and pericentromeric heterochromatin are accessible in living Schizosaccharomyces pombe cells Article Snippet: .. Methylation reactions were performed by adding 0, 25, 50, 100 or 200 U Polymerase Chain Reaction:Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table ) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table ), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis. Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table S1) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table S1), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Purification:Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table ) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table ), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis. Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table S1) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table S1), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Recombinant:Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table ) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table ), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available Article Title: Highly sensitive detection of DNA methyltransferase1 triggered by methylation protection Article Snippet: Type 2 diabetes is on the rise year by year, and 80 % of patients with type 2 diabetes die from cardiovascular complications.. Strict control of blood glucose can significantly reduce the occurrence and development of diabetic microvascular complications, but can not effectively prevent the occurrence of diabetic macrovascular lesions.. DNA methyltransferase 1 (DNMT1) plays an important role in developing phenotypic switching and secretion of inflammatory factors in vascular smooth muscle cells(VSMC), leading to the deregulation of vascular function. Article Title: Targeted Deletion of the Cytopathogenic Toxin A Gene in Sneathia vaginalis. Article Snippet: A region of the CptA_KO_erm plasmid was amplified by PCR using primers TestPCRFWD and TestPCRREV (Table S1) and Phire DNA polymerase master mix (Thermo). .. The PCR product, which contained a single, central GATC site (Table S1), was purified using the PCR purification kit (Qiagen), and 1 μg of the purified test substrate was incubated with 3 μg (10 nM) purified recombinant VC03_04590 or 2.5 U of commercially available |