Copy Number Formula:
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The DNA copy number calculation determines the number of DNA molecules per microliter based on the DNA concentration and length. This is essential for molecular biology applications like qPCR, sequencing, and cloning.
The calculator uses the copy number formula:
Where:
Explanation: The equation converts mass concentration to molar concentration and then to molecular count.
Details: Accurate copy number determination is crucial for quantitative PCR (qPCR) standard curves, next-generation sequencing library preparation, and ensuring consistent DNA input in molecular biology experiments.
Tips: Enter DNA concentration in ng/µL and DNA length in base pairs. Both values must be positive numbers. For best results, use accurate measurements from a spectrophotometer or fluorometer.
Q1: Why is 660 g/mol used for DNA base pairs?
A: This is the average molecular weight of a DNA base pair (dNTP), accounting for different nucleotide compositions.
Q2: Does this work for both single-stranded and double-stranded DNA?
A: The formula is designed for double-stranded DNA. For single-stranded DNA, you would need to adjust the molecular weight calculation.
Q3: What's the typical copy number range for qPCR?
A: Standard curves typically range from 10^1 to 10^9 copies/µL, depending on the target abundance and detection limit.
Q4: How does DNA purity affect the calculation?
A: Impurities (proteins, RNA) can cause concentration measurements to overestimate actual DNA content, leading to inaccurate copy numbers.
Q5: Can this be used for RNA copy number calculation?
A: No, RNA calculations require different molecular weight values (average 340 g/mol per base for single-stranded RNA).