ライフサイエンスコーパス: polybrene

1 time, and concentration of polycation (e.g., Polybrene).

2 ed without the use of exogenous cytokines or polybrene.

3 hat designed fibers exceed the efficiency of polybrene, a commonly used enhancer of transduction.

4 ted into inward surfing after treatment with Polybrene, a soluble cation that increases virus-cell ad

5 ted by culture from 1 of 8 rebound patients; Polybrene addition increased this to 5 of 8.

6 sin, papain, tunicamycin, neuraminidase, and polybrene, allowed Ag-specific TCR capping.

7 Addition of Polybrene and centrifugation enhanced, but polysulfonate

8 ficantly increased by using a combination of Polybrene and plates coated with CH-296 recombinant fibr

9 Both Polybrene and poly-l -lysine significantly enhanced the

10 rticles, was not enhanced by the addition of polybrene, and was inhibited by chloroquine.

11 The use of Polybrene as a self-coating reagent in conjunction with

12 ally increased by a facilitator, for example polybrene, DEAE-dextran or a liposome.

13 A capillary coating of polybrene-dextran sulfate-polybrene (PB-DS-PB) was emplo

14 In the presence of Polybrene, FasL VP killed targets that are resistant to

15 en the capillary was coated dynamically with polybrene, IGF-I and -II could be resolved in a BSA samp

16 Moreover, combining VSV with ruxolitinib and Polybrene or DEAE-dextran successfully broke the resista

17 dramatically improved by treating cells with Polybrene or DEAE-dextran.

18 in the presence of the polycationic polymer Polybrene or when centrifugal forces were applied during

19 In the absence of Polybrene, particle diffusion allows for an outward flow

20 er bilayer consisting of a cationic layer of Polybrene (PB) and an anionic layer of dextran sulfate (

21 We also examined the role of Polybrene (PB) in these interactions.

22 pillary coating of polybrene-dextran sulfate-polybrene (PB-DS-PB) was employed to prevent adsorption

23 However, with polybrene pre-treatment, the nanocomplex could achieve G

24 n IGF-I analog used as an internal standard, polybrene recoating was required after as few as 12 runs

25 for virus used alone or with the polycation Polybrene, showed first-order dependence on virus concen

26 was shuttled through the temperature zones, Polybrene was used as a dynamic coating, which resulted

27 Cationic liposomes, but not Polybrene, were able to mediate envelope-independent tra

28 g of VK1 whereas core shell nanostructure of polybrene@ZnO is coated over copper layer for the sensin