Use a pipette.
For optimal growth and experimental results in a 6-well plate, it is recommended to seed around 1-2 million cells per well.
Common cell culture plate sizes used in laboratory settings include 6-well, 12-well, 24-well, 48-well, and 96-well plates. These plates provide different numbers of wells or compartments for growing cells and conducting experiments. Researchers choose the appropriate plate size based on the specific needs of their experiments.
The volume per well in a 384 well plate is typically around 50-100 microliters.
A 96-well plate can hold a total volume of around 300-400 microliters per well.
Cells convert the energy from glucose into ATP (adenosine triphosphate) through a series of chemical reactions in a process called cellular respiration. ATP is the primary molecule used by cells to store and transfer energy for various cellular functions.
For optimal growth and experimental results in a 6-well plate, it is recommended to seed around 1-2 million cells per well.
AML cells in general don't transfect very well & typically die shortly after. My guess is that you cultured ghost-cells for 21 days.
well there are the male cells of the plant and female parts. bees transfer......
the total count includes dead as well as living cells
refined, intellectual, educated, sophisticated, enlightened, well-informed, urbane, highbrow
To call a person cultured is to infer that the person has refined taste, manners and is well educated. Another meaning is used in Biology, when cells grown or propagated in an artificial medium are said to be "cultured".
Common cell culture plate sizes used in laboratory settings include 6-well, 12-well, 24-well, 48-well, and 96-well plates. These plates provide different numbers of wells or compartments for growing cells and conducting experiments. Researchers choose the appropriate plate size based on the specific needs of their experiments.
They are those of the upper class and are well educated and cultured. They are well mannered and smart. They have a wide knowledge of the world and lack naivete and simplicity.
You can transfer more because of the adhesive interactions of the water create that drop in the loop and you can spread it more easily. Also a needle could pierce the gel you transfer to because of its pointy end. The loop on the other hand distributes its force over a greater area so it does not damage the gel. This is a good answer if going from the tube to the plate, but backwards for the actual question. You use a loop to pick up a well isolated colony from your streak plate to introduce into the culture. You also can use a needle, but you won't get as many cells. However, in my work I just use sterilized toothpicks.
Sophisticate, Well-cultured individual, any descriptive noun involving intelligence or cultural proficiency.
48 h (DMEM containing 10% FBS, 5x104 cells/well in a 24-well plate); Wu Wen-Sheng, Oncogene (2003) 22, 955-963
Well ... it kills the cell(s) you took the nucleus out of, (you've got to clean out two) But you kill more cells whenever you scratch you head. (by a thousand times)