Genomic DNA from plasma or serum, extracted and quantified for qualitative or semi-quantitative analysis using a probe-based method
This test checks for the presence or amount of DNA extracted from your blood (plasma or serum) using a specialized probe technique. It may be used to detect genetic material or mutations.
["This test helps assess genetic material in your blood, often used in research or specific diagnostic contexts."]
Key facts at a glance
- LOINC
- 48683-7
- Short code
- Gp B Strep DNA Spec Ql NAA+probe
- Synonyms
- Gp B Strep DNA Spec Ql NAA+probe
- Category
- coagulation
- Sample
- serum
- Container
- Red-top tube (SST)
- Units
- N/A
- Fasting
- false
- Population
- adult
- Sex
- all
- Age range
- 18–65 years
- Method
- probe-amp-tar
- Specimen volume
- 5 mL
- Stability
- Room temperature: 4h, Refrigerated: 24h, Frozen: 7d
- Hemolysis max
- 500
- Lipemia max
- 1000
- Icterus max
- 500
- TAT
- 4–24 hours
- Order
- routine
What This Test Measures
The test analyzes DNA extracted from your blood sample, which includes genetic material from your cells. This DNA is then examined using a probe—a small piece of DNA or RNA designed to bind specifically to certain sequences. The probe helps determine the quantity or presence of particular genetic sequences.
Why It’s Done
Blood-based DNA testing can serve multiple purposes, including research studies, genetic screening, or detecting specific genetic markers. For example, it may be used to investigate hereditary conditions, monitor genetic research projects, or assess cellular health in certain clinical scenarios.
Sample Collection and Preparation
Your blood sample will be drawn from a vein, typically in a clinic or lab. The blood is then processed to separate plasma or serum, where DNA is extracted. This DNA is purified and prepared for analysis using the probe technique.
What to Expect Before or After the Test
No special preparation is usually needed beyond standard blood draw instructions (e.g., fasting may be avoided). After testing, results may take several days to weeks, depending on the lab’s workflow. Follow-up instructions will be provided if needed.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
While this test is often used in research or specialized diagnostics, it can help identify genetic material for conditions like hereditary cancers, genetic disorders, or cellular studies. It may also be part of broader genetic testing panels or biomarker research. Results are interpreted by healthcare providers in the context of your medical history and symptoms.
Frequently asked questions
What does a positive or negative result mean?
How long will I need to wait for results?
Can I fast before this test?
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