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Sentosa SA201 HSV 1/2 Qualitative PCR Test


Description:

Sentosa SA201 HSV 1/2 Qualitative PCR Test

Developed by Vela Diagnostics USA Inc., the Sentosa SA201 HSV 1/2 Qualitative PCR Test is a specialized diagnostic tool designed for the detection of Herpes Simplex Virus (HSV) types 1 and 2. Utilizing advanced Polymerase Chain Reaction (PCR) technology, this diagnostic tool is crucial in providing accurate and timely results.

The primary application of this medical device is in clinical virology, where it is used to detect and differentiate between HSV-1, the common cause of cold sores, and HSV-2, which is typically associated with genital herpes. Both types of HSV infections are lifelong, and the ability to accurately diagnose them is crucial for successful disease management.

One of the defining benefits of the Sentosa SA201 HSV 1/2 Qualitative PCR Test is its high precision and accuracy. It allows for prompt detection and differentiation of HSV 1 & 2 in one single test format. This characteristic can lead to a more efficient diagnostic process, and thus quicker treatment decision-making.

Furthermore, the utilization of Real-Time PCR technology in this medical device allows for an accelerated testing process. This could significantly reduce the wait time for test results, allowing physicians to provide a faster, more accurate and patient-specific treatment plan.

In conclusion, the Sentosa SA201 HSV 1/2 Qualitative PCR Test, not only expands the testing capabilities within clinical virology but also spearheads leading advancements in individualized patient care and treatment.


Primary Use:

Sentosa SA201 HSV 1/2 Qualitative PCR Test

Primarily used in molecular diagnostics, the Sentosa SA201 HSV 1/2 Qualitative PCR Test is a powerful tool designed to detect and distinguish between the Herpes Simplex Virus type 1 (HSV-1) and type 2 (HSV-2).

HSV-1 and HSV-2 are widespread viruses causing a variety of infectious diseases, often characterized by lifelong recurrent symptoms. Reliable detection and differentiation of these two viruses are crucial to aid in the clinical treatment and management of patients.

The Sentosa SA201 uses advanced Polymerase Chain Reaction (PCR) technology to amplify specific regions of the virus's DNA, making it an extremely sensitive and specific method of detection. It's an essential tool in handling samples from patients who present symptoms of herpes infections such as cold sores, genital herpes, or other related conditions.


How it Works

This innovative test kit extracts HSV-1 and HSV-2 nucleic acids from collected samples. These samples could be cerebrospinal fluid (CSF), genital swabs, oral swabs, or vesicular swabs from symptomatic patients. Once the DNA is isolated and purified, the test then uses PCR to amplify the viral DNA if present. This amplified material is then sequenced to identify whether it is HSV-1 or HSV-2.

Its key strength lies in the ability to quickly and accurately differentiate between the two types of the Herpes Simplex Virus, allowing physicians to make informed decisions for their patient's treatment and care.


Key Benefits

The Sentosa SA201 HSV 1/2 Qualitative PCR Test provides a fast, reliable, and highly accurate method for the detection and differentiation of HSV-1 and HSV-2. It gives medical practitioners a vital edge in making accurate diagnoses and providing optimal patient care.


How It Works:

Sentosa SA201 HSV 1/2 Qualitative PCR Test

The Sentosa SA201 HSV 1/2 Qualitative PCR Test is a sophisticated and advanced diagnostic device that has been meticulously crafted to aid in the detection of Herpes Simplex Virus Type 1(HSV-1) and 2(HSV-2).

Technology Utilized

The backbone of this reliable test method is Polymerase Chain Reaction (PCR), an in vitro technique known for its exceptional sensitivity. It is designed to amplify and detect the DNA of HSV-1 and HSV-2 from the clinical samples of patients. Working Principle The test starts by isolating the DNA from patients’ samples using an automated nucleic acid extraction system. Subsequently, the extracted DNA is then amplified on the Sentosa SX Virus Real-Time PCR Thermocycler with HSV specific primer pairs and probes. The probes are fluorescently labeled, enabling the emission of a signal during hybridization to the amplified products.

Ease of Operation and Analysis

Moreover, what sets the Sentosa SA201 HSV 1/2 Qualitative PCR Test apart from traditional methods is its seamless automated workflow from primary sample to result reporting. The kit is pre-loaded with reagents that significantly ease the process, making it user-friendly for every healthcare worker. Upon completion of the amplification phase, the Sentosa SX101 Workflow Management System analyzes the amplification data against the supplied threshold values to determine whether HSV-1 or HSV-2 DNA are detected in each patient sample.

High-Throughput Sequencing

The quality of this test's results is undeniably trustworthy and precise, underpinned by the process of High-Throughput Sequencing. This cutting-edge technique ensures the maximum yield and quality of HSV sequence data, making the Sentosa SA201 HSV 1/2 Qualitative PCR Test an invaluable addition to any medical practice focused on delivering the highest level of patient care.

Manufacturer:

Vela Diagnostics USA Inc.


Status: In Stock


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