t4 dna ligase buffer (New England Biolabs)
99
Structured Review
New England Biolabs
t4 dna ligase buffer
T4 Dna Ligase Buffer, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 2521 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/reaction+buffer/T4+DNA+Ligase+Reaction+Buffer/pm42127148-320-0-4
Average 99 stars, based on 2521 article reviews
T4 Dna Ligase Buffer, supplied by New England Biolabs, used in various techniques. Bioz Stars score: 99/100, based on 2521 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/reaction+buffer/T4+DNA+Ligase+Reaction+Buffer/pm42127148-320-0-4
Average 99 stars, based on 2521 article reviews
t4 dna ligase buffer - by Bioz Stars,
2026-11
99/100 stars
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Chromatin Immunoprecipitation:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Virus:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Recombinant:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Gene Expression:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins ChIP-qPCR:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Real-time Polymerase Chain Reaction:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Qubit:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Generated:Article Title: Structural remodeling and activation of the hdeAB and proVWX operons in response to pH and salt stress. Article Snippet: .. REAGENT or RESOURCE SOURCE IDENTIFIER Antibodies ChIP-grade anti-FLAG antibody Digenodes Cat# C15200209; RRID: AB_3756920 Bacterial and virus strains Escherichia coli K-12 N/A N/A MG1655 ΔendA Rashid et al.28 N/A MG1655 ΔendA stpA::kanRccdB Rashid et al.28 N/A MG1655 ΔendA hns::kanRccdB this paper N/A ΔendA; rpoS::camR this paper N/A ΔendA; ΔstpAFRT ; ΔhnsKan-KEIO this paper N/A ΔendA; ΔrpoSFRT ; ΔstpAFRT; ΔhnsKan-KEIO this paper N/A ΔendA; hns::hns-3XFLAG this paper N/A ΔendA; stpA::stpA-3XFLAG this paper N/A ΔendA;hns::hns-3XFLAG; stpA::kanRccdB this paper N/A ΔendA; stpA::stpA-3XFLAG; hns::kanRccdB this paper N/A Chemicals, peptides, and recombinant proteins Incubation:Article Title: Reconstituting human and SV40 replisomes with Okazaki fragment maturation reveals synchronized leading- and lagging-strand synthesis. Article Snippet: The digested plasmid was purified from an agarose gel using the QIAquick Gel Extraction Kit (QIAGEN). .. The BsaIlinearized DNA was ligated to a 5-fold molar excess pre-annealed fork and incubated in a reaction containing T4 DNA ligase (60,000 units, New England Biolabs), Article Title: Guanine content in the CTCF motif encodes a vulnerability to persistent, alcohol-induced redistribution Article Snippet: Next, digested chromatin was incubated at 65°C for 20 minutes to inactivate DpnII, after which time restriction fragment overhangs were marked with biotin and repaired by incubation at 37°C for one hour in the presence of fill-in master mix (15 ul of 1 mM biotin-14-dATP, 1.5 ul of 10 mM dCTP, 1.5 ul of 10 mM dGTP, 1.5 ul of 10 mM dTTP, 22.5 ul water, and 8 ul of 5 U/ul DNA polymerase I, Large (Klenow) Fragment (NEB M0210)). .. 900 ul ligation master mix was then added and cells incubated with slow rotation overnight (669 ul water, 120 ul of Gel Purification:Article Title: Reconstituting human and SV40 replisomes with Okazaki fragment maturation reveals synchronized leading- and lagging-strand synthesis. Article Snippet: The digested plasmid was purified from an agarose gel using the QIAquick Gel Extraction Kit (QIAGEN). .. The BsaIlinearized DNA was ligated to a 5-fold molar excess pre-annealed fork and incubated in a reaction containing T4 DNA ligase (60,000 units, New England Biolabs), Amplification:Article Title: AMP Deaminase-2 Activators and Regulators Underpinning Cellular Function in Human Fructose and Nucleotide Metabolism Article Snippet: Removal of the first 128 residues of the hAMPD2-2 sequence from the pET28a vector encoding His6-tagged hAMPD2-2 was performed via PCR amplification using Taq polymerase (Invitrogen), a forward primer (Eurofins) containing an NdeI restriction site (5′- GACTCATATGCGGGAGCGTGATGTGCTG-3′) and a reverse primer (Eurofins) with a HindIII restriction site (5′- CCGCAAGCTTGTCGACTTATTG-3′). .. The amplified and purified PCR product and pET28a-hAMPD2-2 were digested in NEB buffer 2 using NdeI and HindIII restriction enzymes (New England Biolabs) and ligated using Purification:Article Title: AMP Deaminase-2 Activators and Regulators Underpinning Cellular Function in Human Fructose and Nucleotide Metabolism Article Snippet: Removal of the first 128 residues of the hAMPD2-2 sequence from the pET28a vector encoding His6-tagged hAMPD2-2 was performed via PCR amplification using Taq polymerase (Invitrogen), a forward primer (Eurofins) containing an NdeI restriction site (5′- GACTCATATGCGGGAGCGTGATGTGCTG-3′) and a reverse primer (Eurofins) with a HindIII restriction site (5′- CCGCAAGCTTGTCGACTTATTG-3′). .. The amplified and purified PCR product and pET28a-hAMPD2-2 were digested in NEB buffer 2 using NdeI and HindIII restriction enzymes (New England Biolabs) and ligated using Polymerase Chain Reaction:Article Title: AMP Deaminase-2 Activators and Regulators Underpinning Cellular Function in Human Fructose and Nucleotide Metabolism Article Snippet: Removal of the first 128 residues of the hAMPD2-2 sequence from the pET28a vector encoding His6-tagged hAMPD2-2 was performed via PCR amplification using Taq polymerase (Invitrogen), a forward primer (Eurofins) containing an NdeI restriction site (5′- GACTCATATGCGGGAGCGTGATGTGCTG-3′) and a reverse primer (Eurofins) with a HindIII restriction site (5′- CCGCAAGCTTGTCGACTTATTG-3′). .. The amplified and purified PCR product and pET28a-hAMPD2-2 were digested in NEB buffer 2 using NdeI and HindIII restriction enzymes (New England Biolabs) and ligated using Ligation:Article Title: Guanine content in the CTCF motif encodes a vulnerability to persistent, alcohol-induced redistribution Article Snippet: Next, digested chromatin was incubated at 65°C for 20 minutes to inactivate DpnII, after which time restriction fragment overhangs were marked with biotin and repaired by incubation at 37°C for one hour in the presence of fill-in master mix (15 ul of 1 mM biotin-14-dATP, 1.5 ul of 10 mM dCTP, 1.5 ul of 10 mM dGTP, 1.5 ul of 10 mM dTTP, 22.5 ul water, and 8 ul of 5 U/ul DNA polymerase I, Large (Klenow) Fragment (NEB M0210)). .. 900 ul ligation master mix was then added and cells incubated with slow rotation overnight (669 ul water, 120 ul of other:Article Title: Negative regulation of T H 17-mediated inflammation by the nuclear receptor REV-ERBβ Article Snippet: Adapter Ligation:Article Title: Phylogenomics and species delimitation in the Scincella silvicola complex (Squamata: Scincidae) reveal deep structure and cryptic diversity across the Atlantic slopes of Mexico. Article Snippet: .. Adapter ligation was performed by adding 1.5 μl of each enzyme-specific adapter to 30 μl of the digested DNA, followed by 3.4 μl of 10× |
