Genomic DNA from Whole Blood – Quantitative Probe-Based Assay
This test measures the quantity of DNA extracted from your blood sample using a specialized probe-based method. It helps assess genetic material for research, screening, or diagnostic purposes.
["This test evaluates your blood’s DNA content, which may support genetic studies or specific clinical evaluations."]
Key facts at a glance
- LOINC
- 6357-8
- Short code
- C trach DNA Ur Ql NAA+probe
- Synonyms
- C trach DNA Ur Ql NAA+probe
- Category
- chemistry
- Sample
- urine
- Container
- Sterile urine container
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- Specimen volume
- 10 mL
- Stability
- Room temperature: 2h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 0
- Lipemia max
- 0
- Icterus max
- 0
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test detects and quantifies the total amount of genomic DNA present in your blood cells. DNA is the genetic material found in all cells, and its concentration can vary based on factors like cell health, blood composition, or specific medical conditions.
How the Test Works
Your blood sample is processed to isolate DNA. A probe-based assay then measures the DNA concentration with high precision, often used for research, genetic screening, or monitoring certain genetic conditions.
Why It Might Be Ordered
Doctors may order this test for research studies, genetic counseling, or to investigate conditions related to DNA integrity, such as certain inherited disorders or blood-related diseases. It may also be used in clinical trials or specialized diagnostic workflows.
Sample Preparation and Collection
You’ll provide a blood sample, typically drawn from a vein. The lab processes it to extract DNA, which is then analyzed. Follow your healthcare provider’s instructions for fasting or preparation if required.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
While DNA concentration in blood can reflect overall cellular health or genetic composition, it is not typically used for diagnosing common medical conditions. Instead, it may be part of broader genetic testing, research, or specialized diagnostic protocols. Abnormal DNA levels could indicate underlying issues like blood disorders or genetic mutations, but further evaluation is needed.
Short name
DNA Test (Whole Blood)
Frequently asked questions
What does a DNA test in blood mean?
How long does it take to get results?
Is this test painful or invasive?
Sources
- 1
- 2Lab Tests OnlineSource
- 3
Click any link to access the full source. PubMed Central (PMC) links provide free full-text access.
This information is for educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment.
This content is for general informational and educational purposes only and is not a substitute for professional medical advice, diagnosis, or treatment. Always seek the guidance of a qualified healthcare provider with any questions you have about a medical condition, and never disregard professional medical advice or delay seeking it because of something you read here.
If you think you may have a medical emergency, call your local emergency number or go to the nearest emergency department immediately.
Medically reviewed by WellAlly Editorial Team Last reviewed August 16, 2026. · Read our editorial policy