Body Fluid DNA Probe Analysis for Genetic Screening (Multiplex Fluorescence In Situ Hybridization)
This test analyzes DNA extracted from your body fluids (such as blood, saliva, or other samples) using a specialized probe to detect specific genetic sequences. It helps identify potential genetic variations that may influence health risks or conditions.
["This test may be used to screen for inherited genetic conditions or assess genetic predispositions in a non-invasive way."]
Key facts at a glance
- LOINC
- 76610-5
- Short code
- S agalact cfb # XXX.body fld NAA+probe
- Synonyms
- S agalact cfb # XXX.body fld 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 uses fluorescent probes to bind to specific DNA sequences within your body fluid sample. These probes light up under a microscope, allowing for the detection of genetic markers that may be associated with certain conditions or traits. The presence or absence of these markers is recorded for analysis.
How the Test Works
This is a qualitative test, meaning it provides a yes/no or present/absent result rather than a quantitative measurement. The probes target particular genetic regions, and the results indicate whether those regions contain the expected genetic material or variations.
Possible Uses
Body fluid DNA testing like this can be used for genetic screening in prenatal care, carrier testing for inherited disorders, or assessing genetic risks for certain diseases. It may also be part of broader genetic counseling evaluations.
Sample Collection and Preparation
A small sample of your body fluid (e.g., blood, saliva, or other approved fluid) is collected and sent to the lab. The DNA is extracted from the sample and prepared for analysis. This process ensures the genetic material is isolated and ready for probe binding.
Clinical interpretation
How abnormal results are interpreted and what conditions they suggest.
Clinical Significance
Short name
Genetic Fluid Probe Test
Frequently asked questions
Why might I need this test?
What does a positive or negative result mean?
Are there any risks or side effects?
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