We narrowed to 17 results for: eng
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TypeProtocol...lab procedure for separating DNA by size (e.g., length in base pairs) for visualization and purification...longer ones. Thus, you can determine the approximate length of a DNA fragment by running it on an agarose gel...ladder (a collection of DNA fragments of known lengths). Last Update: Feb. 20, 2018 Protocol Video Watch...concentration of 10 mg/mL) Gel loading buffer, New England Biolabs B7022S Procedure Pouring a Standard 1% ... be purifying the DNA for later use, use long-wavelength UV and expose for as little time as possible ...
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DNA Quantification
TypeProtocol...absorb different wavelengths of light to varying degrees and most have a specific wavelength that they maximally...based on its absorbance, you need to know the wavelength of light that your substance maximally absorbs... -
Gibson Assembly Protocol
TypeProtocol... (Gibson et al. , 2009). Regardless of fragment length or end compatibility, multiple overlapping DNA ...fragments at a time. Resources and References New England Biolabs (NEB) (Link opens in a new window) sells... window) . Gibson Assembly® is licensed to New England Biolabs by TelesisBio. Gibson DG, Young L, Chuang... -
Protocol - pLKO.1 – TRC Cloning Vector
TypeProtocol...used for ligation, use only long-wavelength UV light. Short wavelength UV light will increase the chance...Materials Material Vendor and catalog # AgeI New England Biolabs (NEB) #R0552S EcoRI NEB #R0101S NEB buffer... -
Protocol - How to Purify DNA from an Agarose Gel
TypeProtocol...gel electrophoresis, which separates DNA by their length in base pairs. Following electrophoresis, you can...cutting out the bands and you will want to use long-wavelength UV for as short a time as possible to get the... -
Ligation Independent Cloning
TypeProtocol... DNA polymerase can create overhangs of varying length (typically 10-12 bp) based on a specific sequence...or tag sequences (where appropriate). The primer length is dependent on the T4 Pol "chew back" reaction... -
Protocol - How to Ligate Plasmid DNA
TypeProtocol...the amount of DNA used in a ligation based on the length of the DNA to get a proper ratio of 3 available...found on the web. Just enter the concentration, lengths of your insert and vector, and what ratio you want... -
Plasmid Cloning by Restriction Enzyme Digest (with Protocols)
TypeProtocol...cells. The problem is that the only version of full-length cDNA you can find for YGOI is in a bacterial expression...enzyme buffer (see (Link opens in a new window) New England Biolabs for more information about restriction ... -
Protocol - How to Design Primers
TypeProtocol...should generally have the following properties: Length of 18-24 bases 40-60% G/C content Start and end... -
Plasmid Modification by Annealed Oligo Cloning (with Protocols)
TypeProtocol.... to ligate an annealed oligo insert of 50bp in length into a 5kb vector, mix 100ng of the vector with... -
Protocol - How to Perform a Diagnostic Digest
TypeProtocol...commercially available restriction enzymes, see New England Biolabs' website . Last Upload: May 18, 2018 Protocol... -
What is Polymerase Chain Reaction (PCR)
TypeProtocol...extension time can be adjusted according to the length of the target sequence. FAQ How do I design primers... -
Virus Protocol - Generating Stable Cell Lines
TypeProtocol...cells for 13 days. lentiCas9-Blast was a gift from Feng Zhang (Addgene plasmid #52962 ) and is described... -
Plasmid Cloning by PCR (with Protocols)
TypeProtocol...temperatures, but you may need to increase your primer length and increase the Tm if you are trying to clone ... -
Isolating a Monoclonal Cell Population by Limiting Dilution
TypeProtocol...loading control. 1 lentiCas9-Blast was a gift from Feng Zhang (Addgene plasmid #52962 ) and is described... -
AAV Production in HEK293 Cells
TypeProtocol... until fully dissolved. Pro-Tip This step is challenging due to the high viscosity of PEG. Stirring under... -
CRISPR Library Amplification
TypeProtocol...Quality Control (QC) Pooled libraries can be challenging and expensive to ensure adequate quality, but...