scholarly journals 3P212 A cell culture condition which prevents anoikis of anchorage dependent cells

2005 ◽  
Vol 45 (supplement) ◽  
pp. S256
Author(s):  
Y. Emoto
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
A Cell ◽  
Cell Culture Condition

scholarly journals 2P209 A cell culture condition which prevents anoikis of MDCK cells

2004 ◽  
Vol 44 (supplement) ◽  
pp. S162
Author(s):  
Y. Emoto ◽  
C. Imafuku ◽  
K. Tawada
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Mdck Cells ◽  
A Cell ◽  
Cell Culture Condition

scholarly journals Basic Structure and Cell Culture Condition of a Bioartificial Renal Tubule on Chip towards a Cell-based Separation Microdevice

2011 ◽  
Vol 27 (9) ◽  
pp. 907 ◽  
Author(s):  
Xiaofang GAO ◽  
Yo TANAKA ◽  
Yasuhiko SUGII ◽  
Kazuma MAWATARI ◽  
Takehiko KITAMORI
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Renal Tubule ◽  
Basic Structure ◽  
A Cell ◽  
On Chip ◽  
Cell Culture Condition

Analysis of Molecular Expression Patterns of Bovine Embryonic Stem-Like Cells Derived by Conventional ES Cell Culture Condition.

2012 ◽  
Vol 87 (Suppl_1) ◽  
pp. 588-588
Author(s):  
Kyung-Jun Uh ◽  
Se-Heon Jeong ◽  
Chi Jeon Yang ◽  
Eui-Bae Jeung ◽  
Sang-Hwan Hyun ◽  
...  
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Expression Patterns ◽  
Embryonic Stem ◽  
Es Cell ◽  
Molecular Expression ◽  
Cell Culture Condition

Characterization of Primary Human Dermal Fibroblasts to Ensure for Instance EMF Exposure Experiments under Comparable Cell Culture Condition

2020 ◽  
Vol 119 (1) ◽  
pp. 118-127
Author(s):  
Valeria Franchini ◽  
Thomas Müller ◽  
Julian M. Haupt ◽  
Patrick Ostheim ◽  
Matthaeus Majewski ◽  
...  
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Dermal Fibroblasts ◽  
Human Dermal Fibroblasts ◽  
Cell Culture Condition

Cell culture condition-dependent impact of AGE-rich food extracts on kinase activation and cell survival on human fibroblasts

2013 ◽  
Vol 65 (2) ◽  
pp. 219-225
Author(s):  
Norbert Nass ◽  
Kristian Weissenberg ◽  
Veronika Somoza ◽  
Stefanie Ruhs ◽  
Rolf-Edgar Silber ◽  
...  
Keyword(s):  
Cell Culture ◽  
Cell Survival ◽  
Culture Condition ◽  
Human Fibroblasts ◽  
Kinase Activation ◽  
Rich Food ◽  
Cell Culture Condition

Structure-stability relationship of anthocyanins under cell culture condition

2018 ◽  
Vol 70 (3) ◽  
pp. 285-293 ◽  
Author(s):  
Jiaojiao Zhang ◽  
Francesca Giampieri ◽  
Sadia Afrin ◽  
Maurizio Battino ◽  
Xiaodong Zheng ◽  
...  
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Structure Stability ◽  
Relationship Of ◽  
Cell Culture Condition

Cell culture condition control in perfusion culture microchamber array

2009 ◽  
Vol 108 ◽  
pp. S157-S158
Author(s):  
Shinji Sugiura ◽  
Koji Hattori ◽  
Toshiyuki Kanamori
Keyword(s):  
Cell Culture ◽  
Culture Condition ◽  
Perfusion Culture ◽  
Cell Culture Condition

Automated cell counting of astrocytes on patterned substrates containing aliphatic and charged properties

1995 ◽  
Vol 53 ◽  
pp. 974-975
Author(s):  
W. Shain ◽  
H. Ancin ◽  
H.C. Craighead ◽  
M. Isaacson ◽  
L. Kam ◽  
...  
Keyword(s):  
Cell Culture ◽  
Cell Attachment ◽  
Culture Method ◽  
Cell Counting ◽  
Data Sets ◽  
Nuclear Staining ◽  
Double Positive ◽  
A Cell ◽  
Wafer Test ◽  
Cell Densities

Neural protheses have potential to restore nervous system functions lost by trauma or disease. Nanofabrication extends this approach to implants for stimulating and recording from single or small groups of neurons in the spinal cord and brain; however, tissue compatibility is a major limitation to their practical application. We are using a cell culture method for quantitatively measuring cell attachment to surfaces designed for nanofabricated neural prostheses.Silicon wafer test surfaces composed of 50-μm bars separated by aliphatic regions were fabricated using methods similar to a procedure described by Kleinfeld et al. Test surfaces contained either a single or double positive charge/residue. Cyanine dyes (diIC18(3)) stained the background and cell membranes (Fig 1); however, identification of individual cells at higher densities was difficult (Fig 2). Nuclear staining with acriflavine allowed discrimination of individual cells and permitted automated counting of nuclei using 3-D data sets from the confocal microscope (Fig 3). For cell attachment assays, LRM5 5 astroglial cells and astrocytes in primary cell culture were plated at increasing cell densities on test substrates, incubated for 24 hr, fixed, stained, mounted on coverslips, and imaged with a 10x objective.

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