Store the Gibson Assembly Master Mix and positive controls at -20°C. Store the competent cells at -80°C. Store the SOC Outgrowth Medium at room temperature. Before use, thaw and vortex the master mix thoroughly and keep on ice. Gibson Assembly Master Mix (2X) NEB 5-alpha Competent E. coli (High Eficiency) SOC Outgrowth Medium.10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the transformation protocol.Driving calculator. Travelmath provides driving information to help you plan a road trip. You can measure the driving distance between two cities based on actual turn-by-turn directions. Or figure out the driving time to see if you need to stop overnight at a hotel or if you can drive straight through. To stay within your budget, make sure you calculate the cost of driving based on your car's ...Ipswich, MA (December 12th, 2012) - New England Biolabs, Inc. (NEB) today released the Gibson Assembly Cloning Kit and online primer design tool, NEBuilder™ , for the cloning of DNA fragments using the Gibson Assembly approach. This kit includes NEB's robust Gibson Assembly Master Mix and NEB 5-alpha competent .To overcome this issue, NEB® has developed a protocol using NEBuilder HiFi DNA Assembly Master Mix to simplify the construction of single/multiple site-directed mutagenesis. The technique, which involves the design of complimentary flanking primers to align fragments, can be readily adapted for SDM applications.In combination with in vivo assembly in yeast, Gibson Assembly was used to synthesize the 1.1 Mbp Mycoplasma mycoides genome. The synthesized genome was transplanted to a M. capricolum recipient cell, creating new self-replicating M. mycoides cells (2). To help select the best DNA assembly method for your needs, please use our Synthetic Biology ...Specification: 10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the ...Store the Gibson Assembly Master Mix and positive controls at -20°C. Store the competent cells at -80°C. Store the SOC Outgrowth Medium at room temperature. Before use, thaw and vortex the master mix thoroughly and keep on ice. Gibson Assembly Master Mix (2X) NEB 5-alpha Competent E. coli (High Eficiency) SOC Outgrowth Medium.NEBuilder Assembly Tool can be used to design primers for your NEBuilder® HiFi DNA Assembly or Gibson Assembly® reactions, based on the entered fragment sequences and the polymerase being used for amplification. ... primer concentration and your primer sequence and the Tm Calculator will guide you to successful reaction conditions ...BsaI-HF ® v2 has been optimized for Golden Gate Assembly. BsaI-HFv2 also works well for any protocol requiring DNA cutting by BsaI. This is the recommended enzyme for any purpose requiring digestion at the recognition sequence: 5′-GGTCTC (N1)/ (N5)-3′. High Fidelity (HF) Restriction Enzymes have 100% activity in CutSmart Buffer; single ...3. Store samples on ice or at –20°C for subsequent transformation. 4. Transform NEB 5-alpha Competent E. coli cells (provided with the kit) with 2 μl of the assembly reaction, following the transformation protocol. This is the protocol for the Gibson Assembly using the Gibson Assembly® Cloning Kit (E5510).For Gibson Master Mix, use 3.75uL in a 5uL total volume (or 7.5uL in a 10uL total volume). Calculating how much DNA to add to your Gibson Reaction: NEB recommends a total of 0.02–0.5 pmols of DNA fragments when 1 or 2 fragments are being assembled into a vector and 0.2–1.0 pmoles of DNA fragments when 4–6 fragments are being assembled. …Annealing: Optimal annealing temperatures for Q5 High-Fidelity DNA Polymerase tend to be higher than for other PCR polymerases. The NEB Tm Calculator should be used to determine the annealing temperature when using this enzyme. Typically use a 10–30 second annealing step at 3°C above the T m of the lower T m primer.The opposite of the dividend payout ratio, here's exactly how to calculate a company's plowback ratio. The opposite of the dividend payout ratio, a company&aposs plowback ratio is ...Formula. moles ssRNA (mol) = mass of ssRNA (g)/ ( (length of ssRNA (nt) x 320.47 g/mol) + 18.02 g/mol) moles of ssRNA ends = moles ssRNA (mol) RNA copy number = moles of ssRNA x 6.022e23 molecules/mol. Note: nucleic acid MW calculations were revised to assume deprotonated phosphate hydroxyls. Choose a DNA, RNA, qPCR calculator …Use the NEB Tm Calculator to estimate an appropriate annealing temperature when using NEB PCR products. Instructions. Select the product group of the polymerase or kit you plan to use. Select the polymerase or kit from the list of products. If needed, modify the recommended primer concentration.Whether you are new to cloning, or having difficulties with an existing experiment, NEB offers a wide selection products, tools and resources that can help you be more efficient and successful with your experiments. To get started, choose the step in the cloning workflow below that you are interested in to find recommended products, videos ...Transformation: NEB 5-alpha Competent E. coli (High Efficiency, NEB #C2987) provided with the NEBuilder HiFi DNA Assembly Cloning Kit are recommended for use for assembled products of less than 15kb. It is also possible to use other NEB competent E. coli strains, with the exception of BL21, BL21 (DE3), Lemo21 (DE3), Nico21 (DE3), and SHuffle ®.Purify the DNA prior to phosphorylation (NEB # T1030 ). Excess salt, phosphate or ammonium ions may inhibit the kinase. If the ends are blunt or 5´ recessed, heat the substrate/buffer mixture for 10 minutes at 70°C. Rapidly chill on ice before adding the ATP and enzyme, then incubate at 37°C. ATP was not added.Q5U Hot Start High-Fidelity DNA Polymerase is a modified version of Q5 ® High-Fidelity DNA Polymerase, a novel thermostable DNA polymerase that possesses 3′ to 5′ exonuclease activity, and is fused to a processivity-enhancing Sso7d domain. Q5U contains a mutation in the uracil-binding pocket that enables the ability to read and amplify templates containing uracil and inosine bases.Gibson Assembly™ employs three enzymatic activities in a single-tube reaction: 5´ exonuclease, the 3´ extension activity of a DNA polymerase and DNA ligase activity. The 5´ exonuclease activity chews back the 5´ end sequences and exposes the complementary sequence for annealing. The polymerase activity then fills in the gaps on the annealed …Gibson Assembly Cloning Kit (NEB #E5510) Important Note: Upon arrival, store the kit components at -80°C. Before use, thaw and vortex the master mix thoroughly and keep on ice. After first use, store the Gibson Assembly Master Mix, SOC Outgrowth Medium, NEBuilder Positive Control and pUC19 Control DNA at -20°C.JCVI has used Gibson Assembly to rapidly synthesize the entire 16,520 bp mouse mitochondrial genome from 600 overlapping 60-base oligonucleotides (3). It was also used in combination with yeast assembly to synthesize the 1.1 Mbp Mycoplasma mycoides genome, which was then activated in a recipient cell to produce the first synthetic cell (1).Ligation Calculator. This tool will calculate the mass of insert required at several molar insert:vector ratios in the range needed for typical ligation reactions. Choose a DNA, RNA, qPCR calculator from NEB, a leader in production and supply of reagents for the life science industry.A calculator helps people perform tasks that involve adding, multiplying, dividing or subtracting numbers. There are numerous types of calculators, and many people use a simple ele...Updated resource links to NEBuilder and Gibson manuals. Minor revisions to About page and NEB Legal disclaimers. v2.2.5 July 8, 2019. Fixed restriction enzyme digest display issue where duplicate sites were shown. Updated Restriction enzyme data files. v2.2.4 June 10, 2019. Added Q5U Hot Start polymerase as a PCR option. v2.2.3 May 6, 2019Gibson Assembly® Chemical Transformation Protocol (E2611) Thaw chemically competent cells on ice. Transfer 50 μl of competent cells to a 1.5 ml microcentrifuge tube (if necessary). If the chemically competent cells are from New England Biolabs, add 2 μl of assembled product to NEB competent cells and go to step 4 directly.Preferences. Load/Save. SplitSet-Lite. Resources. NEBridge Golden Gate Assembly Tool can be used to design primers for Golden Gate DNA Assembly reactions, estimate overhang fidelity, or find optimal Golden Gate break points for long sequences.No Gibson's have worked thus far when using 1:1 equimolar ratios nor 1:2 backbone : insert ratios when using the NEB Bio Calculator. All Gibson Assembly reactions were ran in the thermocycler at ...Gibson Assembly, developed by Dr. Daniel Gibson and his colleagues at the J. Craig Vendor Institute is an effective method for the assembly of multiple DNA fragments. This is accomplished in a single tube isothermal reaction with Gibson Assembly Master Mix. The method utilizes adjacent DNA fragments with complementary ends which can be added ...This feature also enables NEBuilder to be used in certain applications that NEB Gibson Assembly cannot be used for: NEBuilder HiFi removes 5´- and 3´-end mismatches, and can be used in successive rounds of assembly. This saves time by avoiding time-consuming PCR amplification steps. ... New England Biolabs Ltd. is the exclusive Canadian ...Explore math with our beautiful, free online graphing calculator. Graph functions, plot points, visualize algebraic equations, add sliders, animate graphs, and more.Figure 1: Overview of the Gibson Assembly Cloning Method Specification 10 µl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 µl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed withDpnI cleaves only when its recognition site is methylated. Cleavage of mammalian genomic DNA is blocked by overlapping CpG methylation. Methylation-sensitive restriction enzyme. Time-Saver™ qualified for digestion in 5-15 minutes. 100% activity in rCutSmart ™ Buffer (over 210 enzymes are available in the same buffer) simplifying double digests.HiFi DNA Assembly. Assembling DNA fragments is a key part of both synthetic biology techniques and cloning. NEBuilder HiFi DNA Assembly enables virtually error-free joining of DNA fragments, even those with 5´- and 3´-end mismatches. This flexible mix enables simple and fast seamless cloning utilizing a proprietary high-fidelity polymerase.If your insert is smaller than the vector, say if you’re trying to ligate a 1kb insert into a 3kb vector, you’ll need a higher ratio, in this case about a 3:1 molar ratio of insert to vector. If your inserts are very small, even higher ratios may be needed, sometimes as high as 20:1. You can calculate the amount of DNA you need for your ...Specification: 10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the ...HiFi DNA Assembly. Assembling DNA fragments is a key part of both synthetic biology techniques and cloning. NEBuilder HiFi DNA Assembly enables virtually error-free joining of DNA fragments, even those with 5´- and 3´-end mismatches. This flexible mix enables simple and fast seamless cloning utilizing a proprietary high-fidelity polymerase.DpnI cleaves only when its recognition site is methylated. Cleavage of mammalian genomic DNA is blocked by overlapping CpG methylation. Methylation-sensitive restriction enzyme. Time-Saver™ qualified for digestion in 5-15 minutes. 100% activity in rCutSmart ™ Buffer (over 210 enzymes are available in the same buffer) simplifying double digests.Specification: 10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the ...NEBuilder Assembly Tool can be used to design primers for NEBuilder HiFi DNA Assembly or Gibson Assembly reactions.Gibson Assembly, developed by Dr. Daniel Gibson and his colleagues at the J. Craig Vendor Institute is an effective method for the assembly of multiple DNA fragments. This is accomplished in a single tube isothermal reaction with Gibson Assembly Master Mix. The method utilizes adjacent DNA fragments with complementary ends which can be added ...Mix 8μL Water + 10μL Q5 + 1μL Template + 0.5μL each Primer. Prepare the cycles' times and temperatures according to the user's manual and primers' Tm. Use of the NEB Tm Calculator is highly recommended. Prepare a 0.8% agarose gel for PCR products larger than 1kb and 1.5% for products smaller than 1kb. Complement the PCR reaction with ...For GC-rich targets (≥ 65% GC), amplification can be improved by the addition of the 5X Q5 High GC Enhancer. Q5 High-Fidelity DNA Polymerase is unlike typical, lower fidelity PCR enzymes. To determine the optimal annealing temperatures for a given set of primers, use of the NEB Tm Calculator is highly recommended.Please use NEB's Tm Calculator to determine the appropriate annealing temperature for your primer pair and NEB polymerase/buffer of interest. Unlike other calculators, the NEB Tm Calculator takes into consideration buffer components that affect melting temperatures and empirical observations when calculating the optimal annealing temperature ...NEBuilder Assembly Tool can be used to design primers for NEBuilder HiFi DNA Assembly or Gibson Assembly reactions.Gibson Assembly® Master Mix - Assembly (E2611) Protocols.io also provides an interactive version of this protocol where you can discover and share optimizations with the research community.. Optimal Quantities NEB recommends a total of 0.02-0.5 pmols of DNA fragments when 1 or 2 fragments are being assembled into a vector and 0.2-1.0 pmoles of DNA fragments when 4-6 fragments are ...Gibson Assembly® Cloning Kit NEB #E5510S 10 reactions Version 6.0 7/19 ... This product is covered by one or more patents, trademarks and/or copyrights owned or controlled by New England Biolabs, Inc. ... using the Tm calculator found on the NEB website atMolarity Calculator. This tool will calculate the mass needed to generate a solution based on the desired molarity, MW, and volume, or the molarity based on MW, volume, and mass. Choose a DNA, RNA, qPCR calculator from NEB, a leader in production and supply of reagents for the life science industry.This is the protocol for the Gibson Assembly using the Gibson Assembly® Cloning Kit (E5510). ... (NEB) Tech. support phone: +1(800)632-7799 email: [email protected]. New England Biolabs. New England Biolabs. 5. 41. Run; Create an …This tutorial describes the use of the NEBioCalculator web tool module that converts mass to, or from, moles to help plan an NEBuilder HiFi DNA Assembly reaction. For NEBuilder HiFi DNA Assembly: 2-3 fragments: 15-20 nt overlaps, total DNA = 0.03-0.2 pmol, 2 fold molar excess of each insert:vector.Please use the latest supported version at https://nebuilder.neb.com. NEBuilder Assembly Tool can be used to design primers for your NEBuilder HiFi DNA or Gibson Assembly reactions, based on the entered fragment sequences and the polymerase being used for amplification. Basic Usage:10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the transformation protocol.Ipswich, MA and La Jolla, CA (February 7, 2012) - New England Biolabs, Inc. (NEB) and Synthetic Genomics, Inc. (SGI) jointly announce that they have entered into a licensing agreement whereby NEB will introduce a master mix based on Gibson Assembly™, a revolutionary technology developed by Dr. Daniel Gibson and his colleagues at the J ...Restriction enzymes can also be used to generate compatible ends on PCR products. In all cases, one or more restriction enzymes are used to digest the DNA resulting in either non-directional or directional insertion into the compatible plasmid. Genomic DNA, regardless of the source, is typically digested with restriction enzymes that recognize ...NEBuilder Assembly Tool can be used to design primers for your NEBuilder HiFi DNA or Gibson Assembly reactions, based on the entered fragment sequences and the polymerase being used for amplification. Basic Usage: Set preferences, including the number of fragments and the PCR enzyme. Change settings at any time and the results will be instantly ...Functional Testing (Gibson Assembly) - A 20 μl reaction containing 10 μl of 2X Gibson Assembly Master Mix and six 0.05 pmol fragments of pUC19 (five 400 bp fragments and one 2,780 bp fragment, each with a 40 bp overlap) is incubated at 50°C for 60 minutes. Transformation of NEB 5-alpha competent E. coli cells (NEB #C2987) with 2 μl of the ...You will receive 3 separate products when you order this bundle: 2X (NEB #E2621S) and 1X (NEB #C3019H) (competent cells will arrive in a separate box containing dry ice). Store the NEBuilder HiFi DNA Assembly Master Mix and positive controls at -20°C. Store the NEB 10-beta/ Stable Outgrowth Medium at 4°C.The PCR products and linearized vector are treated with the Gibson Assembly Master Mix, and the resulting transformants are screened for mutations by sequencing. FIGURE 1: Site-directed mutagenesis of lacZ using Gibson Assembly. In this example, multiple mutations are introduced into the lacZ gene through overlapping primers followed by PCR.NEBcloner can also be used to determine recommended double digest conditions. If two different incubation temperatures are necessary, choose the optimal reaction buffer and set up reaction accordingly. Add the first enzyme and incubate at the desired temperature. Then, heat inactivate the first enzyme, add the second enzyme and incubate at the ...Molarity Calculator. The calculators on this page are independent and can be used in any order. The calculators are numbered because sometimes the results of one calculator are used as inputs to a later one. 1. Mass from volume & concentration. Concentration: Formula Weight (daltons): Volume: Mass =.Browse NEB's Gibson Assembly products for cloning ... Please review and update your order accordingly If you have any questions, please contact Customer Service at [email protected] or 1-800-632-5227 x 8. Continue. To Request Technical Support. Fill out our Technical Support Form, email us, ...Formula. DNA calculations to convert µg to pmol for double-stranded and single-stranded DNA, convert micrograms of DNA to pmol ends, calculate vector:insert molar ratio and convert OD260 readings to µg/ml. Also calculate molarity of solutions, perform molar conversions, calculate dilutions and perform other calculations common in molecular ...Figure 1: Overview of the Gibson Assembly Cloning Method Specification 10 µl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 µl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed withFigure 1: Overview of the Gibson Assembly Cloning Method Specification 10 µl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 µl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed withTransformation: NEB 5-alpha Competent E. coli (High Efficiency, NEB #C2987) provided with the NEBuilder HiFi DNA Assembly Cloning Kit are recommended for use for assembled products of less than 15kb. It is also possible to use other NEB competent E. coli strains, with the exception of BL21, BL21 (DE3), Lemo21 (DE3), Nico21 (DE3), and SHuffle ®.Overall GPA for NEB class 12 is calculated by. ∑ G P A ( T h) × C r e d i t H o u r ( T h) + G P A ( P r) × C r e d i t H o u r ( P r) T o t a l C r e d i t H o u r. It was quite easy to calculate GPA till grade ten as credit hour of both practical and theory used to be same. But in grade 12 it may vary according to subjects.Please use the latest supported version at https://nebuilder.neb.com. NEBuilder Assembly Tool can be used to design primers for your NEBuilder HiFi DNA or Gibson Assembly reactions, based on the entered fragment sequences and the polymerase being used for amplification. Basic Usage:10 μl of 2X Gibson Assembly Master Mix was incubated with 6 fragments (5 fragments of 400 bp and one of 2,780 bp, with 40 bp overlap, 0.05 pmol each) in a final volume of 20 μl at 50°C for 60 minutes. NEB 5-alpha Competent E. coli (NEB #C2987) were transformed with 2 μl of the master mix/fragment mixture using the transformation protocol.Product Information. The Q5 Site-Directed Mutagenesis Kit enables rapid, site-specific mutagenesis of double-stranded plasmid DNA in less than 2 hours (Figure 1). The kit utilizes the robust Q5 Hot Start High-Fidelity DNA Polymerase along with custom mutagenic primers to create insertions, deletions and substitutions in a wide variety of plasmids.Formula. moles protein (mol) = mass of protein (g)/ (molecular weight (Da)) number of molecules = moles of protein (mol) x 6.022e23 molecules/mol. Choose a DNA, RNA, qPCR calculator from NEB, a leader in production and supply of reagents for the life science industry.Whether you are new to cloning, or having difficulties with an existing experiment, NEB offers a wide selection products, tools and resources that can help you be more efficient and successful with your experiments. To get started, choose the step in the cloning workflow below that you are interested in to find recommended products, videos ...To calculate the number of pmols of each fragment for optimal assembly, based on fragment length and weight, we recommend using NEB's online tool, NEBioCalculator , or using the following formula: pmols = (weight in ng) x 1,000 / (base pairs x 650 daltons) 50 ng of 5000 bp dsDNA is about 0.015 pmols. 50 ng of 500 bp dsDNA is …Formula. moles ssDNA (mol) = mass of ssDNA (g)/ ( (length of ssDNA (nt) x 307.97 g/mol/nt) + 18.02 g/mol) moles of ssDNA ends = moles ssDNA (mol) DNA copy number = moles of ssDNA x 6.022e23 molecules/mol. Note: nucleic acid MW calculations were revised to assume deprotonated phosphate hydroxyls. Previously, they were assumed …NEBioCalculator®. Use this tool for your scientific calculations and conversions for DNA and RNA. Options include conversion of mass to moles, ligation amounts, conversion of OD to concentration, dilution and molarity. Additional features include sgRNA Template Oligo Design and qPCR library quantification.Gibson Assembly Cloning Kit (NEB #E5510) Important Note: Upon arrival, store the kit components at -80°C. Before use, thaw and vortex the master mix thoroughly and keep on ice. After first use, store the Gibson Assembly Master Mix, SOC Outgrowth Medium, NEBuilder Positive Control and pUC19 Control DNA at - 20°C.NEBNext Multiplex Oligos provide adaptors and primers to enable high yield multiplex Illumina library production. The unique hairpin loop structure of the NEBNext Adaptor minimizes adaptor-dimer formation, and NEBNext index PCR primers enable index incorporation during library amplification. For additional information on available indices and ...Ipswich, MA (December 12th, 2012) - New England Biolabs, Inc. (NEB) today released the Gibson Assembly Cloning Kit and online primer design tool, NEBuilder™ , for the cloning of DNA fragments using the Gibson Assembly approach. This kit includes NEB's robust Gibson Assembly Master Mix and NEB 5-alpha competent .Options include conversion of mass to moles, ligation amounts, conversion of OD to concentration, dilution and molarity. NEBuilder Assembly Tool. NEBuilder® Assembly Tool can be used to design primers for your NEBuilder or Gibson Assembly reaction, based on the entered fragment sequences and the polymerase being used for amplification. NEBCloner.Use the NEB Tm Calculator to estimate an appropriate annealing temperature when using NEB PCR products. Select the product group of the polymerase or kit you plan to use. Select the polymerase or kit from the list of products. If needed, modify the recommended primer concentration. Enter primer sequences (with up to 3 ambiguous bases).Product Notes. BamHI-HF® has the same specificity as BamHI (NEB #R0136 ), but it was engineered for reduced star activity. The increased specificity for the BamHI-HF® cut site has increased binding of the enzyme to the DNA. Under enzyme excess conditions the enzyme can remain attached to the DNA during gel electrophoresis.No Gibson's have worked thus far when using 1:1 equimolar ratios nor 1:2 backbone : insert ratios when using the NEB Bio Calculator. All Gibson Assembly reactions were ran in the thermocycler at ...Use the NEB Tm Calculator to estimate an appropriate annealing temperature when using NEB PCR products. Select the product group of the polymerase or kit you plan to use. Select the polymerase or kit from the list of products. If needed, modify the recommended primer concentration. Enter primer sequences (with up to 3 ambiguous bases).. Script. The NEBExpress Cell-free E.coli ProOpen up NEBCloner and select digestion. Next, choo Gibson Assembly Insert Calculator. Single Insert Gibson Reaction Calculator. Please note that this is a generic protocol that assumes an enzyme that functions at 37C / is heat inactivable / uses buffers compatible with Gibson. Check the specifics of your enzyme before proceeding. backbone concentration:ng/uL. Up to 80% GC content can be amplified by adding the One T Gibson Assembly Master Mix (2X) NEB 5-alpha Competent E. coli (High Efficiency) SOC Outgrowth Medium Positive Controls: Gibson Assembly Positive Control 2 overlapping dsDNA fragments for control assembly pUC19 Control DNA for NEB 5-alpha Competent E. coli Required Materials Not Included: DNA Polymerase (for generating PCR products):Mileage Calculator. Use the following mileage calculator to determine the travel distance, in terms of miles, and time taken by car to travel between two locations in the United States, disregarding traffic conditions. This mileage calculator estimates the number of driving miles between two locations in the United States. We generally recommend using Q5 High-Fidelity DNA Polymerase a...
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