Easy access to products and protocols for research use only in the identification of 2019-nCoV based on Centers for Disease Control and Prevention (CDC) recommendations
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Description:
For RNA purification, it is best to use a phenol or phenol:chloroform mixture with a pH of 4.5 to 5.5. Although phenol alone will purify RNA in these extractions, messenger RNA can collect with the DNA at the inter-phase in the complete absence of chloroform. The ratio of phenol to chloroform can vary from no chloroform to a 1:1 mixture, depending on the individual tissue and the character of the RNA being purified. For many applications, a 5:1 ratio of phenol:chloroform is a recommended starting point. The phenol used for extraction protocols must be highly purified and essentially free of contamination by phenolic acid, a product of phenol oxidation. VWR’s phenol products are manufactured from the purest crystalline phenol to ensure optimal results.
Description:
Obtain fast, simple, highly reproducible, and sensitive immunocapture and protein digestion in a single well using Thermo Scientificâ„¢ SMART Digestâ„¢ ImmunoAffinity (IA) Kits.
Description:
Whatman 1PS Phase Separator from Cytiva's business is a hydrophobic filter for routine solvent extraction. Within seconds it retains aqueous phases, while solvent phases flow through.
Description:
The Monarch® Protein separation solution, supplied as a component of the Monarch HMW DNA extraction kit for tissue, is a salt-based solution that is optimized to ensure proteins in tissue and bacteria samples are easily removed during the phase separation of the Monarch HMW DNA extraction workflow.
Description:
The DNA extraction is performed in a 96 deep-well plate, a convenient high-throughput format that allows you to process up to 96 samples or multiple plates in the same run.
Description:
G-Biosciences' FOCUSâ„¢ Membrane Proteins is a rapid and highly reproducible method for preparation of membrane or hydrophobic proteins from biological samples for 2D-gel analysis or other applications
Description:
Fluorescent substrate for carboxypeptidase M. Because the substrate and the cleavage product Dansyl-Ala-OH are equally fluorescent (λex = 340 nm; λem = 495 nm), the product has to be extracted with chloroform. The uncleaved substrate remains in the aqueous phase (at acidic pH).