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Viromag 1000 Magnetic Transduction Reagent
Catalog number:
VM41000
Brand:
OZ Biosciences
Packing:
1 ml
Price:
€ 698.00
Expected delivery time:
5 days
Quantity:
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Product specifications for - Viromag 1000 Magnetic Transduction Reagent
Overview:
Product group:
Molecular Biology
Category:
Transfection / transduction
Subcategory:
Transduction
Properties:
Datasheet:
Datasheet
Research Use Only
UNSPSC:
41116133
Scientific information:
Scientific info:
ViroMag Transduction Reagent is a magnetic nanoparticles formulation dedicated to increase virus infection and transduction capacities; it is suitable for all viruses. Based on the Magnetofection™ technology, this reagent allows concentrating the complete applied dose of viral particles onto cells within minutes, inducing a significant improvement of virus transduction with extremely low vector doses. Due to its specific properties, ViroMag is ideal to infect non permissive cells. This reagent demonstrates an exceptionally high efficiency to promote, control and assist viral transductions so that no molecular biology processes or biochemical modifications are required.
Increases transduction efficiency
Accelerates the transduction process
Efficient for hard-to-infect and non-permissive cells
Concentrates the viral dose onto the cells
Suitable for all type of virus
Synchronise cells adsorption/infection without modifications of the viruses
Additional information:
Synonyms:
VM41000; OZ Biosciences; Viral Transduction; Magnetofection
Ayala VI, Trivett MT, Coren LV, et al. A novel SIV gag-specific CD4(+)T-cell clone suppresses SIVmac239 replication in CD4(+)T cells revealing the interplay between antiviral effector cells and their infected targets. Virology. 2016;493:100-12.
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Azimi SM, Sheridan SD, Ghannad-rezaie M, Eimon PM, Yanik MF. Combinatorial programming of human neuronal progenitors using magnetically-guided stoichiometric mRNA delivery. Elife. 2018;7
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Bär S, Rommelaere J, Nüesch JP. Vesicular transport of progeny parvovirus particles through ER and Golgi regulates maturation and cytolysis. PLoS Pathog. 2013;9(9):e1003605.
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Baranov SV, Baranova OV, Yablonska S, et al. Mitochondria modulate programmed neuritic retraction. Proc Natl Acad Sci USA. 2019;116(2):650-659.
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Berardozzi S, Bernardi F, Infante P, et al. Synergistic inhibition of the Hedgehog pathway by newly designed Smo and Gli antagonists bearing the isoflavone scaffold. Eur J Med Chem. 2018;156:554-562.
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Betanska K, Hönl C, Spindler-barth M, Spindler KD. The importance of exportin and Ran for nucleocytoplasmic shuttling of the ecdysteroid receptor. Arch Insect Biochem Physiol. 2011;76(1):12-21.
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Boylan BT, Moreira FR, Carlson TW, Bernard KA. Mosquito cell-derived West Nile virus replicon particles mimic arbovirus inoculum and have reduced spread in mice. PLoS Negl Trop Dis. 2017;11(2):e0005394.
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Bruun GH, Doktor TK, Andresen BS. A synonymous polymorphic variation in ACADM exon 11 affects splicing efficiency and may affect fatty acid oxidation. Mol Genet Metab. 2013;110(1-2):122-8.
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Burg VK, Grimm HS, Rothhaar TL, et al. Plant sterols the better cholesterol in Alzheimer's disease? A mechanistical study. J Neurosci. 2013;33(41):16072-87.
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Campbell K, Calvo CJ, Mironov S, Herron T, Berenfeld O, Jalife J. Spatial gradients in action potential duration created by regional magnetofection of hERG are a substrate for wavebreak and turbulent propagation in cardiomyocyte monolayers. J Physiol (Lond). 2012;590(24):6363-79.
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