Although a variety of automated cell counting instruments have been developed, **Hemocytometer** remains the most common method used for cell counting around the world. The most frequently used haemocytometer is the **Neubauer** (or ‘**Improved Neubauer**’) chamber. Other haemocytometers include the Burker, Thoma and Fuchs-Rosenthal. Using these, the particles (e.g., leucocytes, erythrocytes, thrombocytes, bacteria, fungus spores, pollen) are visually counted under a microscope.

## GENERAL FEATURES OF THE NEUBAUER’S CHAMBER

Neubauer’s chamber is a thick glass plate with the size of a glass slide (30x70x4mm). The counting region consists of two square shaped ruled areas. There are depressions or the moats on either side or in between the areas on which the squares are marked thus giving an “

**H**” shape.

The ruled area is 3mm2 divided into **9 large squares** each with a 1 mm^{2} area. The large central square (which can be seen in its entirely with the 10X objective), is divided into **25 medium squares** with double or triple lines. Each of these 25 squares are is again divided into **16 small squares** with single lines, so that each of the smallest squares has an area of 1/400 mm^{2}.

The glass cover is a squared glass of width 22 mm. The glass cover is placed on the top of the Neubauer chamber, covering the central area. The ruled area is 0.1 mm lower than the rest of the chamber. So that when a cover slip is kept on the counting region, there is a gap of 0.1 mm (1/10mm) between the cover slip and the ruled area.

## CELL COUNTING AREAS IN NEUBAUER CHAMBER

The counting can be done either in the central large square or in the corner squares, depending on the size of the cells under study.

**WBC Counting Area**

The four large sqaures placed at the corners are used for white blood cell count. Since their concentration is lower than red blood cells a larger area is required to perform the cell count.

**RBC Counting Area**

The large center square is used for RBC counts. As already stated, this area is subdivided into 25 medium sqaures, which in turn are each divided into 16 squares. Of the 25 medium sqaures, only the four corner squares and the center square within the large center square are used to perform RBC counts.

**Platelet Counting Area**

The large center square is used to count platelets. Platelets in all 25 squares within the large center square are counted.

## USING THE NEUBAUER CHAMBER

### 1. Sample Preparation

Depending on the type of sample, a preparation of a dilution with a suitable concentration should be prepared for cell counting. Typically, the concentration range for a cell count with Neubauer chamber is between 250,000 cells / ml and 2.5 million cells / ml. An appropriate dilution of the mixture with regard to the number of cells to be counted should be used. If the sample is not diluted enough, the cells will be too crowded and difficult to count. If it is too dilute, the sample size will not be enough to make strong inferences about the concentration in the original mixture.

### 2. Preparing Neubauer Chamber

Clean the Neubauer chamber and the cover slip with 70% EtOH. Put the glass cover on the Neubauer chamber central area. Use a flat surface to place the chamber, like a table or a workbench.

### 3. Introducing the sample into the Neubauer chamber

With a pipette, carefully draw up around 20 ml of the cell mixture (dilution). Place the pipette tip against the edge of the coverglass and slowly expel the liquid until the counting chamber is full. Capillary action will help to ensure that the counting chamber is full, but care should be taken not to overfill the chamber. A volume of 10 ml is sufficient to fill one counting chamber.

### 4. Microscope focusing and Cell Counting

- Place the Neubauer chamber on the microscope stage. Using the 10X objective, focus both onto the grid pattern and the cell particles.
- As 10X is appropriate for WBC counting, count the total number of cells found in 4 large corner squares.

To count the RBCs and Platelets, the microscope must be switched to 40X objective. Count the cells in the respective areas as stated early. - Write down the amount of cells counted

* If cells are touching the 4 perimeter sides of a corner square, only count cells on 2 sides, either the 2 outer sides or 2 inner sides.*

## CALCULATING THE CELL COUNTS

The total number of cells per microliter of sample can be calculated from the number of cell counted and area counted. This is because the ruled areas of the chamber contain an exact volume of diluted sample. Since only a small volume of diluted sample is counted, a general formula must be used to convert the count into the number of cells/microliter.

The dilution factor used in the formula is determined by the blood dilution used in the cell count. The depth used in the formula is always 0.1. The area counted will vary for each type of cell count and is calculated using the dimensions of the ruled area.

### Example :

Lets calculate total WBC count by using Neubauer counting chamber.

Number of cells counted = **N = 150 (suppose)**

Area Counted = **1 mm ^{2} x 4 = 4 mm^{2} (area of four large corner squares)**

Depth =

**1/10 mm**

Dilution =

**1:20**

Hence WBC/Cubic mm of Whole Blood =

**N x 50 = 150 x 50 = 7,500**

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How is sheared cells taken into account?

Can you plz explain from your example total wbc count is multiplied by 50 how this fifty comes???

how to count fungal spores through this chamber ?

Let N be the no.of wbcs in all the 4 sqaures.

Volume of one wbc square =1×1×0.1=0.1mm3

Volume of 4 wbc squares =0.4mm3

0.4mm3 of wbc squares contain wbcs=N

1mm3 of wbc squares contain wbcs=N/0.4

Multiplying with dilution factor viz20 =N×20/0.4=N×50.

Good attempt.Pls go ahead

I need more explanation on d preparation of d sample. some should pls help

I just purchased 3 Neubauer Chambers. One colleague who used Nageotte hemocytometer wondered my decision, since he emphysized his support from Lutz publication at Transfusion Vol 33 No 5 Pages 409-412, 1993. He mentioned Nageotte calculates WBC in 50 uL, however, Neubauer counts WBC only in 0.1 uL x 5. Sampling bias is his concern. Could you please help me solving this question? Thank you very much!

thanks