Cell Concentration Formula:
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Cell counting using a hemocytometer is a fundamental technique in cell biology and medical laboratories to determine the concentration of cells in a liquid suspension. This method provides accurate cell density measurements for various applications.
The calculator uses the standard hemocytometer formula:
Where:
Explanation: The formula accounts for the dilution of the sample and the specific volume of the hemocytometer chamber to calculate the original cell concentration.
Details: Accurate cell counting is essential for cell culture maintenance, experimental standardization, clinical diagnostics, and research applications where precise cell concentrations are required.
Tips: Enter the number of cells counted, the dilution factor used, and the number of hemocytometer squares counted. All values must be valid (count ≥ 0, DF ≥ 1, squares ≥ 1).
Q1: Why is the dilution factor important?
A: The dilution factor accounts for any pre-count dilution of the sample to ensure accurate concentration calculation of the original undiluted sample.
Q2: How many squares should I count?
A: Typically, 4-5 large squares are counted for better statistical accuracy. The more squares counted, the more reliable the result.
Q3: What is the 10^4 factor for?
A: This conversion factor accounts for the volume of the hemocytometer chamber (0.1 mm depth) and converts the count to cells per mL.
Q4: When should I dilute my sample?
A: Dilute samples when cell concentration is too high to count accurately (typically above 10^6 cells/mL). Ideal counting range is 2.5×10^5 to 2.5×10^6 cells/mL.
Q5: Are there limitations to hemocytometer counting?
A: Manual counting can have human error and variability. For high-throughput or more precise measurements, automated cell counters may be preferred.