Tilted mammalian cell colony propagation dynamics on patterned substrates

2021 ◽  
Vol 146 ◽  
pp. 110841
Author(s):  
Nicolás E. Muzzio ◽  
Claudio M. Horowitz ◽  
Omar Azzaroni ◽  
Sergio E. Moya ◽  
Miguel A. Pasquale
1995 ◽  
pp. 437-447 ◽  
Author(s):  
Vladimir V. Savchenko ◽  
Alexei G. Basnakian ◽  
Alexander A. Pasko ◽  
Sergey V. Ten ◽  
Runhe Huang

2020 ◽  
Author(s):  
Ashley Robinson ◽  
Mackenzie Crow ◽  
Austin Kratz ◽  
Taylor Ritts ◽  
Yewseok K. Suh ◽  
...  

Clonogenic assays are a simple and robust method that allow researchers to characterize mammalian cell line features, including the ability of a single cell to grow into a colony. We have used this assay as a tool in the undergraduate biology laboratory, exposing students to a more specialized form of mammalian cell culture and helping them refine scientific research skills and knowledge. In this article, we share an easy and undergraduate-friendly method of using HeLa cells to carry out clonogenic assays. The methods described include the introduction of different treatments to assess their effect in HeLa cell colony formation. In this laboratory exercise, undergraduate students utilize different cell culture techniques such as growing, harvesting, counting, diluting, staining, and imaging cells. Clonogenic assay, Cytotoxic agents, HeLa cells, Mammalian cell colony formation, undergraduate laboratory, Open Inquiry-Based Curriculum


2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Ashley M. Robinson ◽  
Mackenzie M. Crow ◽  
Austin Kratz ◽  
Taylor Ritts ◽  
Yewseok K. Suh ◽  
...  

2006 ◽  
Author(s):  
Bakhos A. Tannous ◽  
Jan Grimm ◽  
Katherine Perry ◽  
Ralph Weissleder ◽  
Xandra O. Breakefield

1992 ◽  
Vol 68 (05) ◽  
pp. 539-544 ◽  
Author(s):  
Catherine Lenich ◽  
Ralph Pannell ◽  
Jack Henkin ◽  
Victor Gurewich

SummaryWe previously found that human pro-UK expressed in Escherichia coli is more active in fibrinolysis than recombinant human pro-UK obtained from mammalian cell culture media. To determine whether this difference is related to the lack of glycosylation of the E. coli product, we compared the activity of E. coli-derived pro-UK [(-)pro-UK] with that of a glycosylated pro-UK [(+)pro-UK] and of a mutant of pro-UK missing the glycosylation site at Asn-302 [(-) (302) pro-UK]. The latter two pro-UKs were obtained by expression of the human gene in a mammalian cell. The nonglycosylated pro-UKs were activated by plasmin more efficiently (≈2-fold) and were more active in clot lysis (1.5-fold) than the (+)pro-UK. Similarly, the nonglycosylated two-chain derivatives (UKs) were more active against plasminogen and were more rapidly inactivated by plasma inhibitors than the (+)UK.These findings indicate that glycosylation at Asn-302 influences the activity of pro-UK/UK and could be the major factor responsible for the enhanced activity of E. coli-derived pro-UK.


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