Improvement in the suspension-culture production of recombinant adeno-associated virus–LacZ in HEK-293 cells using polyethyleneimine–DNA complexes in combination with hypothermic treatment

2008 ◽  
Vol 50 (2) ◽  
pp. 121 ◽  
Author(s):  
Lei Feng ◽  
Meijin Guo ◽  
Shuxiang Zhang ◽  
Ju Chu ◽  
Yingping Zhuang ◽  
...  
2015 ◽  
Vol 23 (10) ◽  
pp. 1582-1591 ◽  
Author(s):  
Benjamin Strobel ◽  
Benedikt Klauser ◽  
Jörg S Hartig ◽  
Thorsten Lamla ◽  
Florian Gantner ◽  
...  

2015 ◽  
Vol 23 ◽  
pp. S184-S185
Author(s):  
Daniel R. Blessing ◽  
Monique Montavon ◽  
Maria de Jesus ◽  
Lucia Baldi ◽  
Bernard Schneider ◽  
...  

2016 ◽  
Vol 24 ◽  
pp. S183-S184 ◽  
Author(s):  
Daniel R. Blessing ◽  
Bernard Schneider ◽  
Florian M. Wurm ◽  
Nicole Déglon

2006 ◽  
Vol 22 (1) ◽  
pp. 101-106 ◽  
Author(s):  
H LIU ◽  
X LIU ◽  
B WU ◽  
L YE ◽  
X NI ◽  
...  

2016 ◽  
Vol 03 (01) ◽  
Author(s):  
Katsuhisa Sakaguchi ◽  
Nur Khatijah Mohd Zin ◽  
Yuji Haraguchi ◽  
Azuma Takahashi ◽  
Sara Suzuki ◽  
...  

Autophagy ◽  
2013 ◽  
Vol 9 (9) ◽  
pp. 1407-1417 ◽  
Author(s):  
Patience Musiwaro ◽  
Matthew Smith ◽  
Maria Manifava ◽  
Simon A. Walker ◽  
Nicholas T. Ktistakis
Keyword(s):  
Hek 293 ◽  

2005 ◽  
Vol 103 (6) ◽  
pp. 1156-1166 ◽  
Author(s):  
Kevin J. Gingrich ◽  
Son Tran ◽  
Igor M. Nikonorov ◽  
Thomas J. Blanck

Background Volatile anesthetics depress cardiac contractility, which involves inhibition of cardiac L-type calcium channels. To explore the role of voltage-dependent inactivation, the authors analyzed halothane effects on recombinant cardiac L-type calcium channels (alpha1Cbeta2a and alpha1Cbeta2aalpha2/delta1), which differ by the alpha2/delta1 subunit and consequently voltage-dependent inactivation. Methods HEK-293 cells were transiently cotransfected with complementary DNAs encoding alpha1C tagged with green fluorescent protein and beta2a, with and without alpha2/delta1. Halothane effects on macroscopic barium currents were recorded using patch clamp methodology from cells expressing alpha1Cbeta2a and alpha1Cbeta2aalpha2/delta1 as identified by fluorescence microscopy. Results Halothane inhibited peak current (I(peak)) and enhanced apparent inactivation (reported by end pulse current amplitude of 300-ms depolarizations [I300]) in a concentration-dependent manner in both channel types. alpha2/delta1 coexpression shifted relations leftward as reported by the 50% inhibitory concentration of I(peak) and I300/I(peak)for alpha1Cbeta2a (1.8 and 14.5 mm, respectively) and alpha1Cbeta2aalpha2/delta1 (0.74 and 1.36 mm, respectively). Halothane reduced transmembrane charge transfer primarily through I(peak) depression and not by enhancement of macroscopic inactivation for both channels. Conclusions The results indicate that phenotypic features arising from alpha2/delta1 coexpression play a key role in halothane inhibition of cardiac L-type calcium channels. These features included marked effects on I(peak) inhibition, which is the principal determinant of charge transfer reductions. I(peak) depression arises primarily from transitions to nonactivatable states at resting membrane potentials. The findings point to the importance of halothane interactions with states present at resting membrane potential and discount the role of inactivation apparent in current time courses in determining transmembrane charge transfer.


2007 ◽  
Vol 9 (4) ◽  
pp. 475-485 ◽  
Author(s):  
R. M. Johann ◽  
Ch. Baiotto ◽  
Ph. Renaud
Keyword(s):  
Hek 293 ◽  

2010 ◽  
Vol 35 (7) ◽  
pp. 1075-1082 ◽  
Author(s):  
Lina Ji ◽  
Abha Chauhan ◽  
Ved Chauhan

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