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Page 1 of 231For submission to PhytoFrontiers2Title3Highsensitivity ITS realtime PCR assays for detection of Ceratocystis lukuohia and Ceratocystis huliohia4in soil and air samples5Authors6Wade P.
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01
Gather all necessary materials, including high-sensitivity PCR reagents, samples, and appropriate lab equipment.
02
Prepare your samples by extracting nucleic acids from your target material.
03
Set up PCR reaction mixtures according to the manufacturer's protocol, ensuring to include necessary buffers, primers, and nucleotides.
04
Load the prepared reaction mixtures into the PCR plate or tube, ensuring not to introduce contaminants.
05
Place the PCR plate into the real-time PCR machine.
06
Program the real-time PCR machine with the correct amplification conditions, including temperature cycles and duration.
07
Monitor the amplification process in real-time using the machine's software.
08
Analyze the data post amplification to determine the presence and quantity of the target nucleic acids.

Who needs high-sensitivity its real-time pcr?

01
Researchers in the field of molecular biology and genetics.
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Clinical laboratories for pathogen detection and diagnostics.
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Pharmaceutical companies for drug development and clinical trials.
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Environmental testing laboratories for detecting contaminants in samples.
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Veterinary laboratories for animal health diagnostics.
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High-sensitivity its real-time PCR is a molecular diagnostic technique used to detect and quantify specific DNA or RNA sequences in a sample with enhanced sensitivity, allowing for the identification of low-abundance targets.
Typically, laboratories and healthcare providers conducting high-sensitivity its real-time PCR tests for diagnostics and research purposes are required to file the necessary documentation.
To fill out high-sensitivity its real-time PCR documentation, one must provide detailed information about the sample, testing methodology, results, and compliance with required standards and regulations.
The purpose of high-sensitivity its real-time PCR is to enable the early detection of pathogens or genetic mutations, aiding in the diagnosis of diseases, monitoring treatment responses, and conducting research.
The information that must be reported includes the test methodology, sample identification, results, controls used, and interpretation of data as required by regulatory guidelines.
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