However, loading a hemocytometer is a tedious task and variability in user technique can impact the accuracy and precision of results. ❋ Unknown (2009)
For those of you with a little extra money to spend—around $200 to $400—a used microscope and hemocytometer will allow you to check the condition and exact viability of your yeast. ❋ PATRICK HIGGINS (1998)
A hemocytometer is simply a microscope slide with a microscopic grid calibrated to the millionth of a milliliter. ❋ PATRICK HIGGINS (1998)
After treatment, cells were trypsinized, and viable cells were counted using a hemocytometer. ❋ Nadine Rohwer Et Al. (2010)
Cells were then observed using hemocytometer, and cells that have not internalized the dye due to active dye exclusion were counted and converted to percentage viability. ❋ Dimple Notani Et Al. (2010)
Finally, the beads were counted using a hemocytometer to get a concentration of 10 ❋ Yenny Djuardi Et Al. (2009)
The percentage of cells that excluded Trypan blue was determined by counting 100 cells in triplicate per experimental condition in a hemocytometer. ❋ Unknown (2009)
The cells were collected in PBS with 10\% FCS, counted with a disposable hemocytometer ❋ Unknown (2009)
Cell number and cell viability were determined with a hemocytometer and MTT assay respectively .. ❋ Cong Wang (2009)
Currently, cells are typically counted manually under a microscope using a hemocytometer. ❋ Unknown (2009)
Leukocytes were counted on a hemocytometer to quantify total numbers of leukocytes in the BAL fluid. ❋ Unknown (2009)
The manual describes how to collect blood samples from adult mice and mouse pups; determine hematocrit and use a hemocytometer to count cells; and smear, fix, and stain blood films. ❋ Unknown (2009)
Designed to replace the process of counting cells manually under a microscope using a hemocytometer or an expensive desk top automatic cell counter, Millipore's Scepter crams cell counting technology found in much larger instruments into a hand-held device the size of an automated pipette. ❋ Unknown (2009)
Ten µl of this mixture was loaded into hemocytometer, after which cells were counted. ❋ Branislava Janic Et Al. (2009)
Galactose was added to the cultures and allowed to induce expression of HO endonuclease for four hours at 30°C, at which point cell number was assessed by hemocytometer. ❋ Unknown (2008)
One ml SC glycerol / lactate cultures were inoculated with single colonies of cells that had lost pSD196 or pSD120 and grown for 24 hours at 30°C, at which point cell number was determined by hemocytometer count. ❋ Unknown (2008)
