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Text[1]=["","<img src=images/cytomtery.jpg align=left />A powerful technology for characterising and analysing cells. It simultaneously measures and analyses multiple physical characteristics of single suspended cells or particles of 0.2 to 50 micrometers in size, as they move in a fluid stream through a beam of laser light. A flow cytometer can tell us about a cell's (or particle's) relative size, granularity or internal complexity, and fluorescence intensity. The fluidics, optics and electronics systems work together to determine how cells or particles scatter light and emit fluorescence as they pass through the interrogation point. LCG Bioscience uses Becton Dickinson FACSCalibur and FACSCantoII flow cytometers. "]
Text[2]=["","A Cytometric Bead Array (CBA), commonly referred to as a multiplexed bead assay, is a series of spectrally discrete particles that can be used to capture and quantitate soluble analytes of choice simultaneously.  The method is comparable to a sandwich ELISA, but with the ability to mix different capture antibodies within the same sample. This approach allows you to quantitate soluble analytes in samples never previously considered due to sample volume limitations."]
Text[3]=["","<b>Proteomics</b> is the large-scale study of proteins, particularly their structures and functions. Proteins are vital parts of living organisms, as they are the main components of the physiological metabolic pathways of cells. The term 'proteomics' was coined to make an analogy with genomics, the study the genes - the word 'proteome' is a blend of 'protein' and 'genome'. The proteome is the entire complement of proteins, including the modifications made to a particular set of proteins, produced by an organism or system. This will vary with time and distinct requirements, or stresses, that a cell or organism undergoes."]
Text[4]=["","<img src=images/seldi.jpg align=left />The ProteinChip SELDI system uses surface-enhanced laser desorption/ionization (SELDI) technology to detect and calculate the mass of proteins and peptides. The system integrates ProteinChip arrays, a ProteinChip SELDI reader, and ProteinChip SELDI software to analyze samples based on measured time-of-flight (TOF). SELDI system enables direct access to precise mass analysis of peptides and proteins from complex biological samples. By comparing pre- and post-dose samples, differences in protein profiles can be reliably identified."]
Text[5]=["","<img src=images/elisa1.jpg align=left />ELISA (Enzyme-Linked ImmunoSorbent Assay, also called Enzyme ImmunoAssay or EIA) is a biochemical technique used to detect the presence of an antibody or an antigen in a sample. In simple terms, in ELISA an unknown amount of antigen is affixed to a surface (directly or by an immobilised antibody against the antigen), and then a specific antibody is washed over the surface so that it can bind to the antigen. This antibody is linked to an enzyme, and in the final step a substance is added that the enzyme can convert to some detectable signal, be it light or colour."]


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