the RBCs count you mentioned was counted on the 5 small squares inside the middle square. Isn't the area calculation should be 0.2mm x 5 (squares) x 01 (depth)? Take a look at 23:17. I'm confused.
Hi. Thanks for this comment. Each small square in the middle square has an area of 0.04 sq. mm (see 9:36). Since we counted cells in 5 small squares, the total area counted is 0.2 sq. mm (0.04 sq. mm x 5 squares = 0.2 sq. mm).
In RBC COUNT, WHAT DO YOU MEAN BY TOP AND BOTTOM CHAMBER while you are saying we count 5 intermediate chambers? And why are you doing average of them with 2?
There are two counting chambers in the hemocytometer. They are separated by a channel in the middle of the hemocytometer. You need to count the cells in both. A 10% difference in the counts between the two chambers is indicative of faulty charging. In these cases, you need to repeat the charging process.
Thanks A Lot for this complete Explanation!! Finally got it!! Its never too late! Please continue with this excellent resource!!👍🏼👏🏼
Thank you so much. you are owsome. keep up your work. you may not know but some people really depend on your presentation. god bless you 🙏🙏🙏🙏
the RBCs count you mentioned was counted on the 5 small squares inside the middle square. Isn't the area calculation should be 0.2mm x 5 (squares) x 01 (depth)? Take a look at 23:17. I'm confused.
Hi. Thanks for this comment. Each small square in the middle square has an area of 0.04 sq. mm (see 9:36). Since we counted cells in 5 small squares, the total area counted is 0.2 sq. mm (0.04 sq. mm x 5 squares = 0.2 sq. mm).
Thanks for the clarification!
Kinda didn't get the part in rbc count where you got the area ? The one with 0.02 and 0.04 as you said
the area of the each different intermediate square in the center square is 0.04 square millimeters.
@@ClinicalLabScienceVideos oooh THANKS BRO!
V HELPFUL!!!! thank you🙇🏻♀️
Great video! Thanks
Thanks for the help!
Why dilution factor of 1: 20 is 20 but not 21?
how can I downloads it
In RBC COUNT, WHAT DO YOU MEAN BY TOP AND BOTTOM CHAMBER while you are saying we count 5 intermediate chambers? And why are you doing average of them with 2?
There are two counting chambers in the hemocytometer. They are separated by a channel in the middle of the hemocytometer. You need to count the cells in both. A 10% difference in the counts between the two chambers is indicative of faulty charging. In these cases, you need to repeat the charging process.
Thank you this is so helpful!!
THANK YOU SO MUCH
💗
❤️
Pharmacy students gather here❤