Diagnostics

Cystic Fibrosis

A genetic (inherited) disease that occurs mainly due to mutation in the CFTR genes affecting the lungs and the pancreas, among others. It causes mucus and body fluids to thicken and clog pores and airways, making it difficult for organs to function as desired. Affecting the lungs, it results in shallow, laboured breathing. In the pancreas, it affects the production of enzymes, including insulin, that regulate blood sugar.
* 0 Lakhs
Infected in 2022
* 0
Deaths in 2022

Mylab’s Solutions

Mylab’s CFTR Mutation Detection kit uses the ARMS PCR technology to detect seven major mutations of the CFTR gene. Among its USPs is its ready-to-use nature, robust, high-performance results with accuracy and certainty, and speed of testing in the region of an hour.

Kits

Machines

Compact XL®

Compact XL is a sample-to-PCR-ready system. It automates all lab operations, from sample handling to PCR tube preparation.

Compact DX®

Compact Dx is a Sample-to-Result automation system used for comprehensive molecular testing.

Compact Q

MCompact Q is Fluorescence Quantitative Polymerase Chain Reaction (PCR) Detection System.

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