We narrowed to 41 results for: Kin
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TypeProtocol...sites, will result in similar sized bands, thus making this simple digest less informative. This is particularly...freezer and you are not 100% sure it is what you are looking for, but you have a map and know exactly what it...
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Protocol - How to Inoculate a Bacterial Culture
TypeProtocol...Liquid Bacterial Culture You may also like... Streaking and Isolating Bacteria on an LB Agar Plate Creating...Incubate bacterial culture at 37°C for 12-18 hr in a shaking incubator. Note: Some plasmids or strains require... -
Centrifugation
TypeProtocol...appropriate for the lab space in which you are working. Even if your samples may not require specific ...centrifuge is clean and that everything appears to be working smoothly. Place your sample tubes into the rotor... -
Gibson Assembly Protocol
TypeProtocol... with a two-part Gibson reaction if you're only making a small change in a plasmid (such as point mutations... fine in an assembly if you want to save time. Working on ice, combine segments in the Gibson Assembly... -
Pipetting Protocol
TypeProtocol...amounts of liquid (think: 0.1 µL to 1 mL). When working in a laboratory, properly dispensing liquid ensures...plunger. Remove the entire pipette from the container making sure not to touch the sides of the container with... -
AAV Purification by Iodixanol Gradient Ultracentrifugation
TypeProtocol...syringe and a blunt edge 18 ga Hamilton needle, taking care to avoid bubbles (Figure 1). 8 mL of 15% iodixanol...facing the 40% step. Collect up to 5 mL per tube, taking care to avoid collecting the proteinaceous material... -
Protocol - How to Run an Agarose Gel
TypeProtocol...Wear a lab coat, eye protection and gloves when working with this chemical. Note: If you add EtBr to your...the DNA. Note: When using UV light, protect your skin by wearing safety goggles or a face shield, gloves... -
AAV ddPCR Titration
TypeProtocol...the risk of contaminating reagents we recommend making small aliquots of master mixes, primers, and probes...wells. Cover the cartridge with the DG8 gasket, making sure that it is secure. Transfer the cartridge ... -
CRISPR Library Amplification
TypeProtocol... 30-37 ℃, 225 rpm for 1 hour. After the 1 hour shaking period, pool and gently mix the four tubes. Perform...transformation efficiency! Ensure that no arcing is taking place during electroporation. Arcing would manifest... -
Lentivirus ddPCR Titration
TypeProtocol...wells. Cover the cartridge with the DG8 gasket, making sure that it is secure. Transfer the cartridge ...the risk of contaminating reagents we recommend making small aliquots of master mixes, and primers/probe... -
DNA Quantification
TypeProtocol...DNA is resuspended in, but with no DNA added. 'Blanking' measures the background inherent to the machine... -
Protocol - How to Design Primers
TypeProtocol...regular nucleotide for broader pairing capabilities. Taking into consideration the information above, primers... -
Protocol - How to Create a Bacterial Glycerol Stock
TypeProtocol.... Placing the glycerol stock on dry ice while streaking onto LB agar will prevent it from thawing completely... -
Personal Protective Equipment (PPE) for BSL-1 and BSL-2 Labs
TypeProtocol... (BSL-2). The BSL-1 classification is for labs working with low-risk microbes posing little to no threat... -
Plasmid Modification by Annealed Oligo Cloning (with Protocols)
TypeProtocol... and 3' - G and CAGCT - 5' to the bottom oligo, making our final oligos 34 bp each: Top oligo: 5' - AATTC... -
Protocol - How to Ligate Plasmid DNA
TypeProtocol...efficiency in situations where the 3:1 ratio is not working or when doing more complicated cloning. While 3... -
Using a Light Microscope Protocol
TypeProtocol... until the edges are just out of view. Pro-Tip Looking through a microscope’s eyepiece can take some practice... -
Handling Plasmids from Addgene - Purifying Plasmid DNA
TypeProtocol... Electrophoresis Agarose Gel DNA Purification Streaking and Isolating Bacteria Inoculating a Liquid Bacterial... -
AAV Titration by qPCR Using SYBR Green Technology
TypeProtocol...dilutions. Pro-Tip Make sure that the qPCR is valid by checking to the following: Standard curve: R 2 (coefficient... -
Affinity Purification of Recombinant Antibodies with Protein A or Protein G
TypeProtocol...spectrophotometer 37 °C, 5% CO 2 incubator with shaking platform set to 120 rpm 37 °C bead bath Clamp stand...