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1 time, and concentration of polycation (e.g., Polybrene).
2 ed without the use of exogenous cytokines or polybrene.
4 ted into inward surfing after treatment with Polybrene, a soluble cation that increases virus-cell ad
7 ficantly increased by using a combination of Polybrene and plates coated with CH-296 recombinant fibr
14 en the capillary was coated dynamically with polybrene, IGF-I and -II could be resolved in a BSA samp
15 Moreover, combining VSV with ruxolitinib and Polybrene or DEAE-dextran successfully broke the resista
17 in the presence of the polycationic polymer Polybrene or when centrifugal forces were applied during
19 er bilayer consisting of a cationic layer of Polybrene (PB) and an anionic layer of dextran sulfate (
21 pillary coating of polybrene-dextran sulfate-polybrene (PB-DS-PB) was employed to prevent adsorption
23 n IGF-I analog used as an internal standard, polybrene recoating was required after as few as 12 runs
24 for virus used alone or with the polycation Polybrene, showed first-order dependence on virus concen
25 was shuttled through the temperature zones, Polybrene was used as a dynamic coating, which resulted
27 g of VK1 whereas core shell nanostructure of polybrene@ZnO is coated over copper layer for the sensin
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