Kidney-specific enzyme expression by human kidney cell lines generated through oncogene transfection

1991 ◽  
Vol 148 (1) ◽  
pp. 54-59 ◽  
Author(s):  
Polly S. Robinson ◽  
Charles F. Goochee
Keyword(s):  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney ◽  
Enzyme Expression ◽  
Specific Enzyme

Novel human kidney cell lines for better prediction of nephrotoxicity

2012 ◽  
Vol 29 ◽  
pp. S239
Author(s):  
Lukas Fliedl ◽  
Jens Pontiller ◽  
Sarah Dunzinger ◽  
Paul Jennings ◽  
Matthias Wieser ◽  
...  
Keyword(s):  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney

Alcohol modulation of cloned GABAA receptor-channel complex expressed in human kidney cell lines

1993 ◽  
Vol 631 (1) ◽  
pp. 143-146 ◽  
Author(s):  
Yasutaka Kurata ◽  
William Marszalec ◽  
Beverly J. Hamilton ◽  
Donald B. Carter ◽  
Toshio Narahashi
Keyword(s):  
Gabaa Receptor ◽  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney ◽  
Receptor Channel

Effects of the mycotoxin ochratoxin A and some of its metabolites on human kidney cell lines

2003 ◽  
Vol 17 (4) ◽  
pp. 441-448 ◽  
Author(s):  
G. Müller ◽  
B. Burkert ◽  
H. Rosner ◽  
H. Köhler
Keyword(s):  
Ochratoxin A ◽  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney

Generation and characterization of human kidney cell lines stably expressing recombinant human PTH/PTHrP receptor: lack of interaction with a C-terminal human PTH peptide.

Endocrinology ◽  
1994 ◽  
Vol 135 (4) ◽  
pp. 1713-1716 ◽  
Author(s):  
M Pines ◽  
A E Adams ◽  
S Stueckle ◽  
R Bessalle ◽  
V Rashti-Behar ◽  
...  
Keyword(s):  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney ◽  
Pthrp Receptor

Determination of cytotoxicity of nephrotoxins on murine and human kidney cell lines

2007 ◽  
Vol 43 (1) ◽  
pp. 71-74 ◽  
Author(s):  
Eun-Kee Park ◽  
Sally K. Mak ◽  
Dietmar Kültz ◽  
Bruce D. Hammock
Keyword(s):  
Cell Lines ◽  
Kidney Cell ◽  
Human Kidney

scholarly journals Characterization and optimization of extracellular enzymes production by Aspergillus niger strains isolated from date by-products

2021 ◽  
Vol 19 (1) ◽  
Author(s):  
Reda Bellaouchi ◽  
Houssam Abouloifa ◽  
Yahya Rokni ◽  
Amina Hasnaoui ◽  
Nabil Ghabbour ◽  
...  
Keyword(s):  
Aspergillus Niger ◽  
Culture Medium ◽  
Extracellular Enzymes ◽  
Enzyme Expression ◽  
Specific Enzyme ◽  
Enzymatic Production ◽  
High Production Rate ◽  
High Production ◽  
Incubation Temperatures ◽  
By Products

Abstract Background This work aims to study the optimal conditions of the fermentation culture medium used for the production of extracellular enzymes (amylase, cellulase, lipase, and protease) from previously isolated Aspergillus niger strains in date by-products. Results The five most powerful isolates selected based on the zone of degradation formed on Petri plates by the substrate were subjected to the quantitative evaluation of their enzymatic production. All five strains showed almost similar API-ZYM profiles, with minor variations observed at the level of some specific enzyme expression. The production of cellulase and amylase was depending on pH and incubation temperatures. ASP2 strain demonstrated the high production rate of amylase (at pH 5 and 30 °C) and cellulase (at pH 6 and 30 °C) for 96 h of incubation. Conclusion The A. niger showed the ability to produce several extracellular enzymes and can be used in the valorization of different agroindustrial residues.

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