And you usually get maybe a dozen blank slides and a a few coverslips, which is barely enough to get started. ❋ Bob Thompson (2009)
The only thing we use them for is to clean coverslips and microscope lenses. ❋ Image Goddess (2007)
Anyway I guess I am off to prep more RNA, because I'm worried my cells might not last until tomorrow if I blow it off, and possibly stain some coverslips, mostly because I'm worried I will be too lazy to come in and do it tomorrow. ❋ Unknown (2005)
And our lab has a habit of breaking the matching coverslips at an alarming rate. ❋ Unknown (2005)
I also stained a whole mess of coverslips, but at this rate I won't make it to the microscope I already missed the slot I signed up for, although it seems unlikely anybody else would care on a sunny day! ❋ Unknown (2005)
Bacteria were incubated in chambers containing glass polylysine-coated coverslips and after 72 h the wells were emptied and washed. ❋ Cira Daniela Rinaudo Et Al. (2010)
Post digestion the myocytes were resuspended in DMEM (Dulbecco's Minimum Eagle Media) plus 5% fetal bovine serum (FBS) and approximately 20,000 cells were plated on laminin-coated coverslips and incubated for 2 hours. ❋ Jennifer Davis Et Al. (2010)
Bacteria were grown on uncoated glass coverslips for 72 h in static conditions. ❋ Cira Daniela Rinaudo Et Al. (2010)
Dissociated cardiomyocytes were allowed to attach to laminin-precoated glass coverslips before fixation for immunocytochemistry. ❋ Ting-Ting Hong Et Al. (2010)
Fresh media was introduced every 3-4 days and cells seeded onto 22 mm glass coverslips. ❋ Rodney P. O'Connor Et Al. (2010)
Moreover, cells plated on extracellular matrix-coated coverslips showed enhanced invadopodia formation in response to ❋ J T Lucas (2010)
In a similar manner, coverslips containing primary hippocampal neurons were loaded with the ratiometric dye Fura-PE3 AM (Calbiochem). ❋ Rodney P. O'Connor Et Al. (2010)
Bacteria were grown under static conditions at 37°C for 72 hours on glass coverslips. ❋ Cira Daniela Rinaudo Et Al. (2010)
The arrangement of the TEM cells was chosen to facilitate placement of the mounted coverslips into the microscope light path. ❋ Rodney P. O'Connor Et Al. (2010)
The cells on coverslips were fixed with 4% paraformaldehyde in PBS for 15 min and washed with PBS five times. ❋ Shigeyuki Kanazawa Et Al. (2010)
After washing the cells with ice-cold PBS, we coated the cells with fluorescent mounting medium (Dako), covered them with glass coverslips, and observed the stained cells with a Nikon Fluorescence Microscopy (Nikon, Japan). ❋ Yonghui Zhang Et Al. (2010)
Dissociated cardiomyocytes were allowed to attach to laminin-precoated glass coverslips before fixation. ❋ Ting-Ting Hong Et Al. (2010)
