restriction enzymes asci (New England Biolabs)
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restriction enzymes asci
Restriction Enzymes Asci, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1247 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/restriction+enzymes+asci/AscI/pmc12969024-258-13-16
Average 97 stars, based on 1247 article reviews
Restriction Enzymes Asci, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 97/100, based on 1247 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/restriction+enzymes+asci/AscI/pmc12969024-258-13-16
Average 97 stars, based on 1247 article reviews
restriction enzymes asci - by Bioz Stars,
2026-09
97/100 stars
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Clone Assay:Article Title: Identification of fidelity-determined residues of Porcine reproductive and respiratory syndrome virus through structural alignment Article Snippet: .. The mutated fragment was then cloned into the backbone plasmid, digested with Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Fragments were then fused using an Overlap PCR and cloned into the plant expression vector pMDC32mCherry ( ) using the Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: AtLDAP1 and ScLDAP1 mutants were synthesized by the DNA synthesis services provided by Gene Universal Inc. .. Genes were amplified using the appropriate forward and reverse primers from vectors containing synthesized genes, and cloned into pMDC32mCherry ( ) using the Plasmid Preparation:Article Title: Identification of fidelity-determined residues of Porcine reproductive and respiratory syndrome virus through structural alignment Article Snippet: .. The mutated fragment was then cloned into the backbone plasmid, digested with Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Fragments were then fused using an Overlap PCR and cloned into the plant expression vector pMDC32mCherry ( ) using the Article Title: Host cells and their use for producing ribitol and further monosaccharides Article Snippet: .. The resulting fragment was subcloned into the same vector used for cloning of expressing of wild type ribitol dehydrogenases by restriction digestion with Homologous Recombination:Article Title: Identification of fidelity-determined residues of Porcine reproductive and respiratory syndrome virus through structural alignment Article Snippet: .. The mutated fragment was then cloned into the backbone plasmid, digested with Cloning:Article Title: Identification of fidelity-determined residues of Porcine reproductive and respiratory syndrome virus through structural alignment Article Snippet: .. The mutated fragment was then cloned into the backbone plasmid, digested with Article Title: Host cells and their use for producing ribitol and further monosaccharides Article Snippet: .. The resulting fragment was subcloned into the same vector used for cloning of expressing of wild type ribitol dehydrogenases by restriction digestion with Polymerase Chain Reaction:Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Fragments were then fused using an Overlap PCR and cloned into the plant expression vector pMDC32mCherry ( ) using the Expressing:Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Fragments were then fused using an Overlap PCR and cloned into the plant expression vector pMDC32mCherry ( ) using the Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Article Title: Host cells and their use for producing ribitol and further monosaccharides Article Snippet: .. The resulting fragment was subcloned into the same vector used for cloning of expressing of wild type ribitol dehydrogenases by restriction digestion with Amplification:Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: .. Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: AtLDAP1 and ScLDAP1 mutants were synthesized by the DNA synthesis services provided by Gene Universal Inc. .. Genes were amplified using the appropriate forward and reverse primers from vectors containing synthesized genes, and cloned into pMDC32mCherry ( ) using the Electrophoresis:Article Title: Trends and prevalence of Listeria monocytogenes at poultry abattoirs in Taiwan 2014-2024. Article Snippet: Listeria monocytogenes (L. monocytogenes) is a Gram-positive bacterium and a significant foodborne pathogen that causes listeriosis and occurs in animal products and other foods.. Information on the prevalence of L. monocytogenes in poultry carcasses at abattoirs across Taiwan is limited.. This study investigated L. monocytogenes contamination in poultry carcasses at abattoirs across Taiwan from 2014 to 2024, covering chickens (2014–2024), ducks (2019–2024) and geese (2020–2024) slaughter lines. Ligation:Article Title: Host cells and their use for producing ribitol and further monosaccharides Article Snippet: .. The resulting fragment was subcloned into the same vector used for cloning of expressing of wild type ribitol dehydrogenases by restriction digestion with Synthesized:Article Title: The jojoba lipid droplet protein LDAP1 facilitates the packaging of wax esters into lipid droplets Article Snippet: AtLDAP1 and ScLDAP1 mutants were synthesized by the DNA synthesis services provided by Gene Universal Inc. .. Genes were amplified using the appropriate forward and reverse primers from vectors containing synthesized genes, and cloned into pMDC32mCherry ( ) using the Control:Article Title: Intravenous oncolytic vaccinia expressing transgenes for enhanced safety, inhibition of shedding, imaging, and systemic cancer immunotherapy Article Snippet: Codon-optimized transgene sequences of WT HSV-TK and HSV-TK variants TK.007, SR39, and dm30 were synthetized with the P-SE/L synthetic early-late promoter and homologous flanking regions for the ΔJ2R insertion site (GenScript, Piscataway, NJ) and liberated from the pUC57 plasmid via PCR amplification. .. Viral genomic DNA from the control virus was purified and digested with the Article Title: Intravenous Oncolytic Vaccinia Expressing Transgenes for Enhanced Safety, Inhibition of Shedding and Systemic Cancer Immunotherapy Article Snippet: 393 All the modifications in the viruses described in Table 1 were generated using the same 394 procedure by recombination and reactivation of vaccinia virus DNA.39 Codon optimized 395 transgene sequences of wild type (WT) HSV-TK and HSV-TK variants TK.007, SR39, and 396 dm30 were synthetized with the P-SE/L synthetic early-late promoter and homologous flanking 397 regions for the ΔJ2R insertion site (GenScript, Piscataway, NJ) and liberated from the pUC57 398 plasmid via PCR amplification. .. Viral genomic DNA from the control virus was purified40 and 399 digested with Virus:Article Title: Intravenous oncolytic vaccinia expressing transgenes for enhanced safety, inhibition of shedding, imaging, and systemic cancer immunotherapy Article Snippet: Codon-optimized transgene sequences of WT HSV-TK and HSV-TK variants TK.007, SR39, and dm30 were synthetized with the P-SE/L synthetic early-late promoter and homologous flanking regions for the ΔJ2R insertion site (GenScript, Piscataway, NJ) and liberated from the pUC57 plasmid via PCR amplification. .. Viral genomic DNA from the control virus was purified and digested with the Article Title: Intravenous Oncolytic Vaccinia Expressing Transgenes for Enhanced Safety, Inhibition of Shedding and Systemic Cancer Immunotherapy Article Snippet: 393 All the modifications in the viruses described in Table 1 were generated using the same 394 procedure by recombination and reactivation of vaccinia virus DNA.39 Codon optimized 395 transgene sequences of wild type (WT) HSV-TK and HSV-TK variants TK.007, SR39, and 396 dm30 were synthetized with the P-SE/L synthetic early-late promoter and homologous flanking 397 regions for the ΔJ2R insertion site (GenScript, Piscataway, NJ) and liberated from the pUC57 398 plasmid via PCR amplification. .. Viral genomic DNA from the control virus was purified40 and 399 digested with Purification:Article Title: Intravenous oncolytic vaccinia expressing transgenes for enhanced safety, inhibition of shedding, imaging, and systemic cancer immunotherapy Article Snippet: Codon-optimized transgene sequences of WT HSV-TK and HSV-TK variants TK.007, SR39, and dm30 were synthetized with the P-SE/L synthetic early-late promoter and homologous flanking regions for the ΔJ2R insertion site (GenScript, Piscataway, NJ) and liberated from the pUC57 plasmid via PCR amplification. .. Viral genomic DNA from the control virus was purified and digested with the |