Specifications include, but are not limited to: Appropriately sized system for gel electrophoresis and capillary electrophoresis system for approximately 6500 serum proteins, 2500 serum immunotyping, 4500, hemoglobin electrophoresis,1500 urine protein, and 500 urine immunotyping tests annually. Instrumentation/Methodology: • Must have FDA approval for Serum and Urine protein, Serum and Urine Immunotyping, and Hemoglobinopathies by capillary electrophoresis technology, on a single platform. • Must be fully automated from primary tube to result. • Must have automated primary tube sampling. • Must have cap piercing technology for whole blood assays. • Must have onboard samples mixing for whole blood assays. • Must be for use on K2 and K3 EDTA as anticoagulant blood collection tubes for whole blood assays. • Must have intended use for detection of major hemoglobin variants including S, C, D, E. • Must run at least 45 hemoglobin tests / hr. • Must have no interference on quantitation of HbA2 in the presence of HbS or HbC. • Must have on board bar code reader for full traceability with positive sample and rack ID. • Must be able to load more than two racks of patient samples at a single time for Hb analysis. • Must use same capillaries for all assays offered on platform. • Must have temperature controlled capillaries. • Reagents must be RFID tagged for full traceability. • Must have unlimited database storage. • Must have ability to recall past result and overlay on current pattern for comparison purposes. • Must utilize one software across gel and capillary platforms. • Software must have multi-tasking capability using windows menus. • Must have capability to link patient results across multiple assays. • Must have networking capabilities to link multiple databases together. • Must have on-board quality control including statistic program with Levy-Jennings. • Must have minimal reagent and control preparation. • Must have no sample pre-treatment requirements. • Methodology must provide an adequate reportable range. • Methods will demonstrate accuracy and precision with analyte appropriate coefficients of variation. • Proven bi-directional interface capability, including curve transmission, through Data Innovations and host query capability. Must be operational to satisfaction within 60 days of installation. • Equipment must support multiple barcode formats that may be enabled concurrently. • Equipment must accept, at a minimum, a 10-character specimen identifier (20- character flexibility is preferred) that is alphanumeric (letters and numbers). • Equipment must be able to store and retransmit records in case of interface outage. • Software for operation of the system should be windows driven, user friendly, with point and click icons for easy operation (desirable). • Must include interface credit for connecting to laboratory information system.