Hepatitis C Viral RNA Genotype 1 NS5a Drug Resistance Test sale cost 12000 AED
Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test sale cost 9360 AED Prenatal Diagnosis Panel 1 Chorionic Villus Biopsy Test 10,400 د.إ Original price was: 10,400 د.إ.9,360 د.إCurrent price is: 9,360 د.إ.
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Hepatitis C Viral RNA Genotype 1 NS5a Drug Resistance Test

Original price was: 18,200 د.إ.Current price is: 12,000 د.إ.

-34%

The “Hepatitis C Viral RNA Genotype 1 NS5a Drug Resistance Test” is a specialized diagnostic procedure designed to detect resistance mutations in the NS5a region of the hepatitis C virus (HCV) genotype 1. This test is particularly crucial for tailoring the most effective antiviral therapy for individuals infected with HCV, as resistance mutations can significantly impact the efficacy of treatment regimens. The test involves analyzing the viral RNA to identify specific mutations within the NS5a protein, which plays a key role in the virus’s replication process and its resistance to NS5a inhibitor drugs.

Given the complexity and precision required for this test, it is performed at specialized laboratories equipped with advanced molecular diagnostic technologies. In the UAE, DNA Labs UAE is one of the facilities offering this cutting-edge test, ensuring high accuracy and reliability in the results. The cost for undergoing the Hepatitis C Viral RNA Genotype 1 NS5a Drug Resistance Test at DNA Labs UAE is 12,000 AED. This investment is crucial for optimizing the management and treatment of HCV, particularly for patients with genotype 1, the most common and often the most challenging to treat variant of the virus. By identifying the presence of drug resistance mutations, healthcare providers can make informed decisions on the most appropriate and effective treatment strategies, potentially improving patient outcomes and reducing the risk of treatment failure.

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HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test

Welcome to DNA Labs UAE, where we offer the HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test. This test is designed to diagnose and assess the drug resistance of Hepatitis C Virus (HCV) genotype 1 NS5a.

Test Components

  • HCV NS5a Subtype
  • Daclatasvir Resistance
  • Ledipasvir Resistance
  • Ombitasvir Resistance

Price

The cost of the HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test is AED 12,000.0.

Sample Condition

For the test, we require 2 mL (1 mL) of plasma in 1 Lavender top (EDTA) tube or 2 mL (1 mL) of serum in 1 SST. Please separate the plasma/serum aseptically within 8 hours of collection and ship it refrigerated or frozen. It is mandatory to fill the Test Send Out Consent Form.

Report Delivery

The sample should be sent by the 7th of the month, and the report will be delivered after 2-3 weeks.

Method

The HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test utilizes Polymerase Chain Reaction (PCR) and Sequencing techniques.

Test Type

This test is specifically designed to diagnose and assess the drug resistance of Hepatitis C Virus (HCV) genotype 1 NS5a, which is a disease of the liver.

Doctor

This test is recommended to be performed under the supervision of a Gastroenterologist.

Test Department

The HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test is conducted in our OS department.

Pre Test Information

It is mandatory to fill the Test Send Out Consent Form before undergoing the HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test.

Test Details

The HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test is a genetic test that analyzes the exome of three individuals within a family unit. It focuses on the proband, who is affected by a genetic disorder, and both of their biological parents. By analyzing the exome, this test can identify genetic variants that may be responsible for causing a genetic disorder or increasing the risk of developing one. The test utilizes next-generation sequencing (NGS) technology to analyze millions of DNA sequences simultaneously. It can detect single nucleotide variants (SNVs), small insertions and deletions (indels), and structural variants (SVs) such as copy number variations (CNVs) and inversions. The test can also identify de novo mutations, which are genetic changes that occur spontaneously and are not inherited from either parent. The HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test is used to diagnose genetic disorders, identify carriers of genetic disorders, and assess the risk of developing certain genetic disorders. It can also provide information about the inheritance pattern of a genetic disorder, aiding in family planning and genetic counseling.

Test Name HEPATITIS C VIRAL RNA GENOTYPE 1 NS5a DRUG RESISTANCE Test
Components *HCV NS5a Subtype*Daclatasvir Resistance *Ledipasvir resistance*Ombitasvir Resistance
Price 12000.0 AED
Sample Condition 2 mL (1 mL) plasma in 1 Lavender top (EDTA) tube OR2 mL (1 mL) serum in 1 SST. Separate plasma \/ serum asepticallywithin 8 hours of collection. Ship refrigerated or frozen. Duly filled Test Send Out Consent Formis mandatory.\n\n\n\n.
Report Delivery Sample by 7th of the month; Report after 2??3 weeks
Method Polymerase Chain Reaction, Sequencing
Test type Disease of Liver
Doctor Gastroenterologist
Test Department: OS
Pre Test Information Duly filled Test Send Out Consent Formis mandatory.
Test Details

The NGS Gen Whole Exome Sequencing Trio Test is a genetic test that analyzes the exome of three individuals within a family unit: a proband (the individual who is affected by a genetic disorder), and both of their biological parents. The exome is the part of the genome that codes for proteins, which are the building blocks of the body. By analyzing the exome, this test can identify genetic variants that may be responsible for causing a genetic disorder or increasing the risk of developing one.

The NGS Gen Whole Exome Sequencing Trio Test uses next-generation sequencing (NGS) technology to analyze millions of DNA sequences simultaneously. The test can detect single nucleotide variants (SNVs), small insertions and deletions (indels), and structural variants (SVs) such as copy number variations (CNVs) and inversions. The test can also identify de novo mutations, which are genetic changes that occur spontaneously and are not inherited from either parent.

The NGS Gen Whole Exome Sequencing Trio Test is used to diagnose genetic disorders, identify carriers of genetic disorders, and assess the risk of developing certain genetic disorders. The test can also be used to provide information about the inheritance pattern of a genetic disorder, which can help with family planning and genetic counseling.

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