The MultiSUB Choice offers a wide degree of versatility. Three tray options are available; 15 x 7cm, 15 x 10cm and 15 x 15cm – allowing the choice of one, two or all three gel length options at the time of purchase. Further purchases of additional accessories are no longer required. Maximising comb and tray options allow up to 210 samples to be resolved per gel. The 15cm total run length allows restriction fragment or other close MW sample bands to be easily separated and identified. Speed loading is accomplished using 10, 14, 16, 18, 28 or 30 sample multi-channel pipette compatible combs.Fabricated MultiSUB choice stretch units are available with optional 15 x 20cm and 15 x 25cm gel trays and four 28-sample combs for those researchers wanting to perform higher resolution separation of more samples over a longer distance. MultiSUB Choice Trio includes all 3 tray sizes for optimum versatility and value.
MultiSUB Choice ST
A ‘stretched’ version of the MSCHOICE, this system is perfect for extended high-resolution separations of samples from 96-well microplates and blokcs, using its 15 x 20cm and 15 x 25cm gel trays and four 28-sample multichannel compatible combs. It may also be used for routine preparatory techniques.
Catalogue Page Number: 14
This product has been cited in the following research papers:
|Effect of the linear aliphatic amine functionalization on in vitro transfection efficiency of chitosan nanoparticles
||Gök, M.K., Demir, K., Cevher, E., Özgümüş, S. and Pabuccuoğlu, S., 2018. Effect of the linear aliphatic amine functionalization on in vitro transfection efficiency of chitosan nanoparticles. Carbohydrate Polymers.
||…perature while stirring on magnetic stirrer at 200 rpm. pEGFN1 loading capacity on the surface of the nMChi, Chi nanoparticles (nChi) and DNA integrity was assessed by 4% agarose gel electrophoresis (Cleaver Scientific Ltd., England).…
|DNA damage in hair root cells as a biomarker for gamma ray exposure
||Semra Tepe Çam, Nesrin Seyhan, Mutation Research/Genetic Toxicology and Environmental Mutagenesis, Volume 756, Issues 1–2, 30 August 2013, Pages 201-205,
||…ere immersed for 1 h in a lysing solution (2.5 M NaCl, 100 mM EDTA, 10 mM Tris, 1% Triton X-100, 10% DMSO) at 4 °C. The slides were then placed in an electrophoresis unit (MSCHOICE, MP-250 N omniPAC, cleaver scientific Ltd., Warwickshire, UK) containing a buffer (300 mM NaOH, 1 mM EDTA, pH 13) for 40 min at room temperature to allow for DNA unwinding. Electrophoresis was then carried out for 30 mi…