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The NucliSens® HIV-1 QT is an in vitro nucleic acid amplification test designed for the quantitation of Human Immunodeficiency Virus Type 1 (HIV-1) RNA in human plasma. It is used for monitoring
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How to fill out nuclisens hiv-1 qt

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How to fill out NucliSens® HIV-1 QT

01
Collect the sample following appropriate guidelines.
02
Prepare the sample for testing by centrifuging if necessary.
03
Add the appropriate lysis buffer to the sample to release RNA.
04
Mix the sample and lysis buffer thoroughly.
05
Load the sample into the NucliSens® HIV-1 QT cartridge.
06
Insert the cartridge into the NucliSens® extractor machine.
07
Select the correct test protocol on the machine.
08
Start the extraction process and wait for results.

Who needs NucliSens® HIV-1 QT?

01
Individuals who are at risk of HIV infection.
02
Patients undergoing HIV testing for diagnosis.
03
Healthcare providers managing HIV patients.
04
Laboratories conducting HIV research and surveillance.
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People Also Ask about

The Aptima HIV-1 RNA Qualitative Assay is an in vitro nucleic acid assay system for the detection of human immunodeficiency virus (HIV-1) in human plasma and serum. It is intended for use as an aid in the diagnosis of HIV-1 infection, including acute or primary infection.
HIV/AIDS Glossary The state of either having or not having detectable antibodies against a specific antigen, as measured by a blood test (serologic test). For example, HIV seropositive means that a person has detectable antibodies to HIV; seronegative means that a person does not have detectable HIV antibodies.
Answer. Both the PCR and the DUO tests look for all subtypes of the two strains, HIV-1 and HIV-2. It does not matter where you were infected geographically, these tests are designed to pick up any infection.
HIV-1 RT is a heterodimer that contains two related polypeptides of 66 kDa (p66) and 51 kDa (p51). The polymerase domain of HIV-1 RT comprises the N-terminal 440 amino acid residues of the p66 subunit. The ribonuclease H (RNase H) domain comprises the remaining 120 amino acid residues at the C terminus of p66.
Interpret results as follows: Reactive for HIV-1 antibodies: Two coloured lines appear, one in the control region “C” and one in the test region “T1”. Reactive for HIV-2 antibodies: Two coloured lines appear, one in the control region “C” and one in the test region “T2”.
An enzyme found in HIV (and other retroviruses). HIV uses reverse transcriptase (RT) to convert its RNA into viral DNA, a process called reverse transcription.
The treatment for HIV is called antiretroviral therapy (ART). ART involves taking a combination of HIV medicines daily, monthly, or every other month. While ART cannot cure HIV, prompt HIV treatment can help all people with HIV live long, healthy lives and reduce the risk of HIV transmission.
How is this test done? Rapid HIV testing is done with a sample of either blood or saliva. For a blood sample, a needle is used to draw blood from a vein in your arm or hand. For a saliva sample, your healthcare provider will rub a special swab against your gums.

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NucliSens® HIV-1 QT is a quantitative assay used for measuring the viral load of HIV-1 in plasma samples. It helps in monitoring the effectiveness of antiretroviral therapy and guiding treatment decisions.
Healthcare providers, including laboratories and clinicians who perform HIV testing and monitoring, are required to file NucliSens® HIV-1 QT results for patients undergoing treatment for HIV-1.
To fill out NucliSens® HIV-1 QT, healthcare providers must accurately complete the required fields including patient identification, sample collection date, and test results. Ensure compliance with local regulations regarding documentation.
The purpose of NucliSens® HIV-1 QT is to quantify HIV-1 viral RNA levels in a patient's blood. This information is critical for assessing disease progression, determining therapy effectiveness, and making clinical decisions regarding antiretroviral treatment.
The information that must be reported includes patient demographics, test results (viral load), test date, and details of the healthcare provider conducting the test. Additional clinical information may also be required based on local guidelines.
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