Laboratory Infrastructure

• Comprehensive test menus for enzymes, substrates & specific protein parameters.
• Customized & pre-measured pack size configuration.
• Parameter reagents available in ready-to-use liquid, stable & lyophilised powder format.
• Specially designed mono vial [1 ml] reagent range provides ease of convenience in analysis.
• Parameter available with different selection of methods (IFCC or DGKC).
• Reagent provides precise sensitivity, wide measurement range & long shelf life stability.
• Long working reagent & on board stability for precise automated analysis.

Labsystems Diagnostics Biocard M.pneumoniae IgM is a rapid test for the detection of IgM antibodies against Mycoplasma pneumoniae from serum fingertip blood or intravenous blood sample.

INCUBATORSHAKER

NS Reader

Biocard™ Combo lateral flow assay kit consists of NS1 antigen along with IgM and IgG detecting the antibody device to completely diagnose the immune profile of Dengue viral infection using the lateral flow assay method.All the accessories needed for the sampling and testing are included.Works on Serum/Plasma and Whole Blood.Results can be obtained in 20 minutes

Washer Module

Biocard Myoglobin is a qualitative rapid immuno chromatographic test for the detection of Myoglobin from human serum samples

• Specific antigens
• Internal and external quality monitoring
• Long shelf life even for opened kit components (6 months)
• Interchangeable reagents and similar procedures

Labsystems Diagnostics’ M. pneumoniae + C. pneumoniae Duplex Real-Time PCR kit is a quantitative PCR assay for the simultaneous and separate detection of Mycoplasma pneumoniae and Chlamydophila pneumoniae in human respiratory samples.This kit is intended to use on respiratory samples after DNA extraction M. pneumoniae + C. pneumoniae Duplex Real-Time PCR, 25 tests, 8100100M. pneumoniae + C. pneumoniae Duplex Real-Time PCR, 100 tests, 8101100M. pneumoniae + C. pneumoniae Duplex Real-Time PCR, 150 tests, 8100101

Congenital adrenal hyperplasia (CAH) refers to a group of autosomal recessive disorders that impair cortisol biosynthesis. CAH represents a continuous phenotypic spectrum with over 95% of all cases caused by 21hydroxylase deficiency. CAH owing to 21hydroxylase deficiency is the most common cause of genital ambiguity in the newborn and is present in about 1 in 15000 live births worldwide

Labsystems Diagnostics’ Neonatal Phenylalanine is a chemical method, with fluorometric detection, for quantitative determination of phenylalanine from blood specimens dried on filter paper, intended for newborn screening for phenylketonuria (PKU).