Mylab - Proud Partner For Molecular Testing

About Mylab

Mylab is a biotechnology company that develops & commercializes diagnostic kits and instrumentation to empower la bs to obtain Reliable, Timely & Actionable answers. It operates on an ISO 9001, ISO 13485 certified facility under 98/79/EC Full Quality Assurance Systems,

GMP certified environment. Science and Technology drive our company and our goal is to always be faster than others in delivering high-quality diagnostic solutions to improve lives.

Mylab advantages

  • Asia’s first FDA-approved ID-NAT test kit manufacturer.
  • India’s first ICMR-approved Covid-19 RT-PCR Kit manufacturer.
  • World’s First High-throughput Point-of-Care molecular diagnostics platform detecting Covid-19 using RT-PCR method branded as CoviSwift.
  • FDA-approved & CE-IVD marked real-time PCR kits with ISO13485 manufacturing
  • Automatable Solution – The technology can be used as standalone (manually), at the same time can be integrated with Automated platform for Highest sensitivity & Highest Specificity, making it matching or better than any existing commercial kit
  • Unique Formulation – Unique and robust Proteinase K formulation making it cost-effective and stable at room temperature.
  • Multiplexing Capability – Mylab’s Unique formulation of Multiplex compatible Enzyme and Multiplex primer probe detection mix makes the process – Easy, Fast, and Cost-effective.
  • Single Tube Run – Unique sequences of Oligos (primers) and Fluorescent oligos (probes) are used in a method of enhancing detection capacity in a Single Real-time PCR reaction.
  • Cost-effective solution where only one single reaction will detect multiple diseases.
  • Highly-efficient Performance – RT and Taq polymerase available in optimized buffer component in such a way that 5OuI of PCR reaction gives similar/better results with that of 1OOuI PCR reaction of competition platform – Saving huge costs The low concentration of detection mix is further achieved with unique reconstitution/dilution buffer to improve the PCR efficacy.

HPV detection Test (Type 16/18) by PCR

The Mylab Discovery solutions PathoDetectTM HPV PCR Detection Kit (type 16/18) is an in vitro diagnostic kit designed for detection of both Human Papilloma Virus (HPV) type 16 and 18 DNA extracted from variety of human samples including cervical swabs, cervico-vaginal samples, tissue etc. This diagnostic test kit utilizes the RT-PCR for HPV 16/18 detection.

Kit Features

  • Accurate: Highly sensitive and specific detection of HPV 16 and 18
  • Safe: Low contamination risk – no post-PCR product handling
  • Fast: Results within 90 minutes after PCR start
  • Quality Controlled: Inclusion of internal control gene to assess the performance of both nucleic acid extraction and real time PCR
  • All Included: Includes all the reagents required to perform sample to Result analysis
  • Direct Results: Direct to customer clinical lab tests based on RT-PCR
  • Easy to use: Simple reaction setup and data interpretation

Mylab HIV Quantitative PCR Kit

The PathoDetectTM HIV quantitative PCR kit is an in vitro nucleic acid amplification test for the quantitation of based on real time PCR technology, for the detection and quantification of HIV specific RNA encompassing all HIV-1 groups M subtypes and Group N. Human Immunodeficiency Virus (HIV) RNA in human plasma. This diagnostic test kit utilizes the real time polymerase chain reaction (PCR) after nucleic acid extraction

Kit Features

  • Direct to customer” Robust clinical lab tests based on real time PCR
  • Nucleic acid detection and quantitation of HIV-1 (Group M)
  • Testing of individual blood sample provides ultra- sensitive results
  • Includes all the reagents required to perform sample to Result analysis.
  • Inclusion of controls for quality check ensures high security and result reliability;
  • Calibrators provided for viral load calculations
  • Fast – Results in under 4 hrs starting from sample to result analysis
  • Low contamination risk – no post-PCR product handling
  • High-throughput – can screen up to 90 samples in a single run

MTB -RIF/INH Detection Test

Mylab Discovery Solutions provides real time PCR based rapid detection of target sequence of M. tuberculosis complex and internal control in a single tube. High sensitive and specific for detection of mycobacterium tuberculosis complex (MTC) The real time assay uses the Taqman fluorogenic probe based chemistry that uses the 5´ nuclease activity of Taq DNA polymerase and enables the detection of a specific PCR product as it accumulates during PCR cycles. This test detects MTB and also drug sensitivity for Rifampicin and Isoniazid.

Kit Features

  • Direct to customer” clinical lab tests based on real time PCR
  • High sensitive and specific for detection of mycobacterium tuberculosis complex (MTC)
  • Includes all the reagents required to perform sample to Result analysis
  • Inclusion of positive and negative controls for quality check
  • Inclusion of internal control gene to assess the PCR inhibition
  • Cost effective and rapid test
  • Low contamination risk – no post-PCR product handling
  • High-throughput – can screen up to 46 samples in a single 96-well run
  • Fast – results in under 80 minutes after PCR start
  • Simple reaction setup and data interpretation

Mylab HBV Quantitative PCR Kit

The PathoDetectTM HBV quantitative PCR kit is an in vitro nucleic acid amplification test for the quantitation of hepatitis B virus (HBV) DNA in human plasma. This diagnostic test kit utilizes the real time polymerase chain reaction (PCR) after nucleic acid extraction.

Kit Features

  • Direct to customer” Robust clinical lab tests based on real time PCR
  • Nucleic acid detection of HBV genome of Genotype A-G
  • Testing of individual blood sample provides ultra- sensitive results
  • Includes all the reagents required to perform sample to Result analysis.
  • Inclusion of controls for quality check ensures high security and result reliability
  • Calibrators provided for viral load calculations
  • Fast – Results within 4 hrs. starting from sample to result analysis
  • Low contamination risk – no post-PCR product handling
  • High-throughput – can screen up to 90 samples in a single run

Mylab HCV Quantitative PCR Kit

The PathoDetectTM HCV quantitative PCR kit is an in vitro nucleic acid amplification test for the quantitation of hepatitis C virus (HCV) RNA in human plasma. This diagnostic test kit utilizes the reverse transcription polymerase chain reaction (RT-PCR). The viral load is measured using a range of four quantification calibrators provided in the kit. The PathodetectTM HCV quantitative PCR kit is not intended to be used as a screening test for HCV or as a diagnostic test to confirm the presence of HCV infection.

Kit Features

  • Direct to customer” Robust clinical lab tests based on real time PCR
  • Nucleic acid detection and quantitation of HCV genome of Genotype 1-6
  • Testing of individual blood sample provides ultra- sensitive results
  • Includes all the reagents required to perform sample to Result analysis.
  • Calibrators provided for viral load calculations
  • Fast – Results within 5 hrs starting from sample to result analysis
  • Low contamination risk – no post-PCR product handling
  • High-throughput – can screen up to 90 samples in a single run

NAAT Testing or Triple H

The Mylab Discovery Solutions NATSpert ID TripleH detection Kit offers all in one qualitative multiplex RealTime PCR test for simulteneous detection and discrimination of HIV, HBV and HCV in a single tube format. TM NATSpert ID TripleH is licensed by FDA for screening of Human Immunodeficiency Virus type 1 (HIV) Group-M RNA, HIV-1 Group-O RNA, HIV-2 RNA, Hepatitis C Virus (HCV) RNA and Hepatitis B Virus (HBV) DNA in human plasma specimens from individual human donors, blood products and suspected individuals. The NATSpert provides viral nucleic acid extraction using Mylab’s proprietary magnetic bead technology. Extracted viral nucleic acid is further amplified using real time PCR technology for detection and discrimination of HIV RNA (HIV-1 Groups M and O RNA, HIV-2 RNA), HCV RNA (Genotype 1-6) and HBV DNA (Genotype A-H) . The test also incorporates a heterologous Internal Control (IC) to be processed during extraction and real time PCR for monitoring test performance for each individual sample, this ensures high reliability of NATSpert ID Triple H detection kit, with it’s stringent quality check.

Types of Viruses covered

  • HIV-1 genotype( A to H including AE and GH)
  • HIV-1 Group O RNA
  • HIV-2 RNA
  • HCV RNA (Genotype 1-6)
  • HBV DNA (Genotype A-H)

Mylab HLA B27 Detection Kit

Human leukocyte antigen (HLA) B27  is a class I surface antigen encoded by the B locus in the major histocompatibility complex (MHC) on chromosome 6. The human leucocyte antigen (HLA) B*27 is strongly associated with the spondyloarthropathies (SpA’s). HLA-B*27 is found in 90-95% of ankylosing spondylitis (AS) patients and also lesser frequency in forms of psoriatic arthritis and reactive arthritis. HLA-B*27 may have a direct role in the pathogenesis of SpA. There are more than 50 subtypes of HLA-B27 identified which mostly differ by only a small number of nucleotides. Allele specific PCR offers excellent specificity and sensitivity for HLA-B*27 genotype. Mylab Lifesolutions HLAB*27 Detection test is an in vitro diagnostic test for the detection of HLAB*27 genotypes as an aid to diagnosis in the evaluation of patients with suspected ankylosing spondylitis by allele specific real time PCR.

Kit Features

  • Highly Sensitive allele specific real time PCR for detection of HLAB*27 genotype
  • Inclusion of endogenous control as a quality check for whole procedure
  • Easy workflow with ready-to-use solutions and optimal quality control
  • Simple reaction setup and data interpretation
  • Includes all reagent required to perform Sample to Result analysis no additional reagents needed.
  • Low contamination risk – no post-PCR product handling
  • High-throughput – can screen up to 90 samples in a single run
  • Fast – results within 80 minutes after PCR start
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