Products

The SARAQ^® Hepatitis B (HBV) Viral Load Real-time PCR Test Kit is used to quantify the HBV genotypes A-H from Blood plasma/serum samples of patients confirmed to have HBV Infection. The test includes an internal control to identify possible qPCR inhibition and verify the quality of sample extraction.

The kit includes Ready to Use Master-mix, 5 Quantitative standards, and Negative Control.

Thermal Cycler Compatibility :

FAM^® (Green), Cal Fluor® Red 610 (Orange Channel) Validated against WHO International Standard for Hepatitis B.

IVD Approved

The SARAQ^® Hepatitis C Virus (HCV) Real-time PCR Test Kit is used to quantify the HCV genotypes 1-6 from Blood plasma/serum samples of the patients confirmed to have HCV Infection. The test includes an internal control to identify possible qPCR inhibition and verify the quality of sample extraction.

The kit includes Ready to Use Master-mix, 5 Quantitative standards, and Negative Control.

Thermal Cycler Compatibility :

Quasar® 670 (Red Channel), Cal Fluor® Red 610 (Orange Channel).

Validated against WHO International Standard for Hepatitis C.

IVD Approved

The SARAQ^® CMV Viral Load Real-time PCR Kit is designed for the quantitative detection of Cytomegalovirus (CMV) DNA in human plasma specimens from individuals suspected of CMV infection.

Cytomegalovirus is a member of the Herpesviridae family and may be transmitted through various body fluids, including blood, saliva, urine, semen, and breast milk.

The kit includes an internal control to monitor PCR inhibition and verify nucleic acid extraction performance and specimen quality.

Sample Types:

Human Plasma.

Thermal Cycler Compatibility :

FAM™ (Green Channel), Texas Red/ROX (Orange Channel).

RUO (Research Use Only)

The SARAQ^® BCR-ABL (Quantitative) Real-time PCR Kit is designed for the quantitative detection of Major, Minor, and Micro BCR-ABL fusion transcripts in human blood and bone marrow specimens obtained from patients previously diagnosed with Chronic Myeloid Leukemia (CML) or Acute Lymphoblastic Leukemia (ALL). The kit includes an internal control (ABL PPM) to monitor extraction performance and verify specimen quality.

The kit contains a Ready-to-Use PCR Mix, target-specific Primer-Probe Mixes for Major, Minor, and Micro BCR-ABL transcripts, ABL PPM, PCR Additive, Negative Control, five Quantitative Standards (BCA-S1 to BCA-S5), and Positive Controls. The assay has been validated against the 1st WHO International Genetic Reference Panel for BCR-ABL.

Thermal Cycler Compatibility :

FAM™ (Green Channel) for BCR-ABL Fusion Transcripts; HEX/VIC/JOE (Yellow Channel) for ABL.

RUO (Research Use Only)