WebbThe Thermo Scientific Pierce Protein A Plus Agarose Spin Plate for IgG Screening offers a high-throughput format for quick purification and screening of antibodies and for immunoprecipitation (IP). Each well of … WebbSpecifications Membrane: HPLC certified Maximum operating temperature: 100 °C Housing: Medical grade, virgin polypropylene Autoclave: Sterilize by dry heat at 121 °C for 15 minutes Applications • IC sample preparation and analysis • Dissolution testing Chemical Incompatibilities • Protein-based samples in aqueous solutions • Concentrated …
Desalting and Gel Filtration Chromatography - Thermo …
WebbDepth filtration. In terms of particle retention, filters fall into two categories: surface filters and depth filters. Surface filters, generally referred to as membranes, trap particles exclusively on the top surface. These filters are well suited to samples with low particulate content. However, high particulate content tends to rapidly clog ... WebbOmrix Biopharmaceuticals. nov. 2012 - jul. 20244 jaar 9 maanden. Einstein 14, Ness Ziona, Israel. • Leading of a bio-process development group (3-5 people) • Concept development - drug substances and devices. • Establishment of core protein purification unit under R&D department. • Design and establishment of pilot scale chromatography ... the current density
Thermometer: a webserver to predict protein thermal stability ...
WebbThe filter I used was Thermo Scientific's Nalgene™ Syringe Filters - 25mm Diameter, which is recommended for 10~50mL solution. No wonder when I filtered my 500uL sample through the filter, a ... WebbManager of a research project between industry and academic partners Organizing, conducting and evaluating experiments with focus on: - protein fractionation, purification, characterization, and thermal aggregation - techno-functionality (i.e., interfacial properties and stabilization behavior of foams and emulsions) of native … Webbproteins with MW >20 kDa. For smaller proteins, gel filtration media of a suitable molecular weight cutoff should be selected. Labeled peptides may be separated from free dye by TLC or HPLC. Removal of free dye after a labeling reaction is essential for the accurate determination of dye to protein ratios. For optimal protein recovery the current design is not implemented