Some examples and use cases from the internet:

Some examples and use cases from the internet:

• Examine the stained smear with an epifluorescence microscope at 450 nm under oil immersion at a magnification of 600 to 1000 using an oil
• Flood the fixed smear with 1 % aqueous solution of Nile blue A. Incubate for 10 minutes at 55 ºC.
• Flood the smear with 8 % aqueous acetic acid.
• Flood the smear with 8 % aqueous acetic acid and incubate for one minute at ambient temperature.
• Examine the stained smear with an epifluorescence microscope at 450 nm under oil immersion at a magnification of 1000.
• or water
• Flood the fixed smear with 0,3 % Sudan black B solution in 70 % ethanol.
• Examine the stained smear with a light microscope using transmitted light under oil immersion at a magnification of 1000.

• Smear the mustard over the floor!
• With Smear, the adjacent pixels will spread out to replace the mixing pixels.
• Smear: Emptying places are filled with a spreading of the neighbouring image line.
• Smear: With this option, pixels vacated by displacement are replaced with pixels stretched from the adjacent part of the image.
• Smear: Because of the waves, areas are rendered empty on sides. The adjacent pixels will spread to fill them.
• Get a smear and ultrasound her vessels for plaque.
• Where the edge detector will get adjoining pixels for its calculations when it is working on the image boundaries. This option will only have an effect on the boundaries of the result (if any). Smear is the default and the best choice.
• Confirm with a blood smear And adamts13 antibodies.