Laboratory Infrastructure

Biocard Parvo B 19 is a onestep immuno chromatographic test for the rapid and convenient screening of Parvovirus B 19 antibodies specific for acute phase of disease in serum plasma or whole blood sample swab sample.

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

Exclusive capillary electrophoresis technology for high-resolution separation and complete walk-away automation, from hemolysate preparation to final color-coded results.

Biocard™ Malaria Pf/PAN antigen diagnostic kit is a pLDH Antigen capture test kit for differential detection of Malaria P.falciparum and PAN Malarial species by pLDH antigen capture method.All the accessories needed for the sampling and testing are included.Works on Human Whole blood.Results can be obtained in 20 minutes.

ThinPrep® 5000 ProcessorFully Automated Sample Processor for PAP test

Microtomy at the touch of a button The first of its kind this fully automated and programmable microtome aligns and trims blocks with optimal precision section after section.

Biocard rapid test for determination of antitTG IgA in whole blood is a rapid test kit is based on lateral flow immunochromatography method for qualititative detection of IgA antibodies to tTGAll the accessories needed for the sampling and testing are included.Works on SerumPlasma and Whole Blood.Results can be obtained in 20 minutes

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

Cystic Fibrosis (CF) is an autosomal recessive disorder affecting the lungs, pancreas, intestine and liver. CF is the most common in Caucasians with an incidence rate 1:2500 newborns. CF is caused by mutation in the gene for the protein cystic fibrosis transmembrane conductance regulator (CTFR) [1,2]. Large-scale neonatal screening for CF is performed by indentification of increased levels of immunoreactive trypsinogen (IRT) in blood.

Biocard Helicobacter pylori IgG is an immunochromatographic test for the detection of Helicobacter pylori IgG antibodies in whole fingertip blood intravenous blood or serum samples

Congenital hypothyroidism (CH) is an endocrine disorder of newborns characterized by the decreased levels of thyroid hormones: thyroxine (T4) and triiodothyronine (T3) in periferal blood. In early perinatal period manifestations of CH are often non-specific, subtle or even non-existent [1-2]. However, the disease, if undiagnosed and untreated, leads to severe

• The complete solution for small and mid-sized laboratories
• ThinPrep® Sample Collection
• ThinPrep Cytology Processing
• Compass™ Stainer for slide staining
• ThinPrep Integrated Imager & Imaging System