TALLY 7.2 INTEREST CALCULATION FREE

After charging, wait for 3-5 min so that the cells settle down in the chamber. A volume of 10 Р’Вµl is sufficient to fill out the one counting chamber.This process occurs by Capillary action, but care should be taken not to overfill the chamber. Now gently place the pipette tip against the edge of the cover glass and if required slowly expel the more liquid until the counting chamber is full.Press the knob of the pipette to make a hanging drop at the tip of the micropipette. So, with a micropipette, carefully draw up around 20 Р’Вµl of the diluted specimen. You can also use a micropipette instead of RBC pipette for charging the Hemocytometer.Now, take out the RBC pipette and fill it with the Diluted Specimen, mix the solution well and then discard 1-2 drops from the pipette before charging the chamber.Similarly, clean out the cover glass and place it over the grooved area of Hemocytometer. Take out the NeubauerРІР‚в„ўs chamber / Hemocytometer from its case and clean it using a swab or gauze piece. Mix well for few minutes and ready your Hemocytometer / NeubauerРІР‚в„ўs Chamber.Now add 0.02 ml or 20 Р’Вµl of Blood Specimen to the tube containing diluting fluid with the help of micropipette or RBC pipette.

TALLY 7.2 INTEREST CALCULATION FREE

Take 3.98 ml of RBC diluting fluid in a Clean, Dry and Grease free Test tube.After charging, wait for 3-5 min so that the cells settle down in the chamber & then focus the chamber under the microscope to calculate Red Cells.Do not overcharge the chamber and there should be no air bubble in the Chamber. Allow a small amount of fluid from the pipette to fill into the chamber which occurs by the Capillary action.Touch the Tip of the pipette with the hanging drop against the edge of the coverslip making an angle of 45Р’В° approximately.Gently press the rubber tube of the RBC pipette, so that the next drop of fluid is in hanging position.Now, put the RBC pipette, mix the solution present in it again and then discard 1-2 drops from the pipette before charging the chamber.After doing this interest calculation button will activate and accept the feature form. Open tally 9, and go to features F11 button and click it and yes in the front of activate interest calculation and advance parameters. Similarly, clean out the cover glass and place it over the grooved area of Hemocytometer. There are following steps for interest calculations in tally 9. Take out the NeubauerРІР‚в„ўs chamber / Hemocytometer from its case and clean it using a swab or gauze piece.Mix the Blood and Diluting fluid in the pipette by rotating the pipette (horizontally) between your palms. 12 is what percent of 60 12 is divided by 60 and multiplied by 100: (12 / 60) Р“вЂ” 100 20.Be cautious that there should be no air bubble in the pipette bulb. Step 2 We have the principal value or present. Step 1 We need to name cell E3 as РІР‚ВRateРІР‚в„ў by selecting the cell and changing the name using Name Box. Suppose we have the following information to calculate compound interest in a table excel format (systematically). Fill the same pipette with the RBC diluting fluid (preferably HayemРІР‚в„ўs Fluid) up to the mark 101. Example 2 Using the Compound Interest Calculation Table in excel.Fill the RBC pipette up to the 0.5 mark with the blood specimen and wipe out the pipette externally to avoid false high results.

Tally 7.2 interest calculation