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Ariola, Rhoanna L.
Diamance, Mary Hazel B.
Hemo: blood
Cyto: cell
Meter: measurement/counter
*Thus, it is an instrument used to
count the blood cells.
It includes:
a) Neubauer’s
slide
b) Cover slip
c) micropipette
d) RBC pipette
e) WBC pipette
It is a thick glass slide, center of which has double
ruling area separated by troughs (these four troughs
are extending across the slide and set parallel to
each other. The fifth one is separating the two ruling
areas from each other).
Step 1.
 Put the glass cover on the Neubauer slide central area.
 Take 10 µl sample from a suspension using a
micropipette.
 Introduce it to the Neubauer chamber. When the
pipette is loaded, it must always be held in vertical
position.
 Place pipette tip close to the glass cover edge, right at
the centre of the Neubauer chamber.
 Release the plunger slowly watching how the liquid
enters the chamber uniformly, being absorbed by
capillarity.
 In case of the appearance of bubbles, or that the glass
cover has moved, repeat the operation.
Cell counting
Step 2.
 Place the Neubauer chamber on the
microscope stage.
 Turn on the microscope light..
 Focus the microscope until a sharp image of
the cells is already seen.
 Look for the first counting grid square
where the cell count will start.
1 mm

0.04 mm
Cell counting
Cell counting
Cell density is …..
For bigger
squares:
(A+B+C+D)(2500)
a

b

c

d

e

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Cell counting

  • 2. Hemo: blood Cyto: cell Meter: measurement/counter *Thus, it is an instrument used to count the blood cells.
  • 3. It includes: a) Neubauer’s slide b) Cover slip c) micropipette d) RBC pipette e) WBC pipette
  • 4. It is a thick glass slide, center of which has double ruling area separated by troughs (these four troughs are extending across the slide and set parallel to each other. The fifth one is separating the two ruling areas from each other).
  • 5. Step 1.  Put the glass cover on the Neubauer slide central area.  Take 10 µl sample from a suspension using a micropipette.  Introduce it to the Neubauer chamber. When the pipette is loaded, it must always be held in vertical position.  Place pipette tip close to the glass cover edge, right at the centre of the Neubauer chamber.  Release the plunger slowly watching how the liquid enters the chamber uniformly, being absorbed by capillarity.  In case of the appearance of bubbles, or that the glass cover has moved, repeat the operation.
  • 7. Step 2.  Place the Neubauer chamber on the microscope stage.  Turn on the microscope light..  Focus the microscope until a sharp image of the cells is already seen.  Look for the first counting grid square where the cell count will start.
  • 11. Cell density is ….. For bigger squares: (A+B+C+D)(2500)