A rapid color enhanced hemagglutination slide test for the detection of rheumato
A rapid color enhanced hemagglutination slide test for the detection of rheumatoid factor in serum or synovial fluid
A rapid color enhanced hemagglutination slide test for the detection of rheumato
A rapid color enhanced hemagglutination slide test for the detection of rheumatoid factor in serum or synovial fluid
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which sever
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which several different reagent areas are affixed
JIR,JIL
INDICATOR METHOD, PROTEIN OR ALBUMIN (URINARY, NON-QUANT.),METHOD, ENZYMATIC, GL
INDICATOR METHOD, PROTEIN OR ALBUMIN (URINARY, NON-QUANT.),METHOD, ENZYMATIC, GLUCOSE (URINARY, NON-QUANTITATIVE)
hemochroma PLUS Optical System Check is intended to assure the performance of th
hemochroma PLUS Optical System Check is intended to assure the performance of the optic system of the hemochroma PLUS Analyzer.
hemochroma PLUS Controls are intended for use as quality control material to ass
hemochroma PLUS Controls are intended for use as quality control material to assure the validity and performance of the hemochroma PLUS System in measuring the human hemoglobin concentration.
A rapid color enhanced undiluted latex slide test for the qualitative or semi- q
A rapid color enhanced undiluted latex slide test for the qualitative or semi- quantitative determination of rheumatoid factor in serum
A rapid color enhanced undiluted latex slide test for the qualitative or semi- q
A rapid color enhanced undiluted latex slide test for the qualitative or semi- quantitative determination of rheumatoid factor in serum
The hemochroma PLUS Microcuvettes are used for measurement of hemoglobin concent
The hemochroma PLUS Microcuvettes are used for measurement of hemoglobin concentration in human whole blood along with the hemochroma PLUS Analyzer. The hemochroma PLUS Microcuvette is inserted into a holder of hemochroma PLUS Analyzer for quantification of hemoglobin in blood
The hemochroma PLUS Analyzer calculates the test result automatically and displa
The hemochroma PLUS Analyzer calculates the test result automatically and displays hemoglobin concentration in terms of g/dL.
A rapid undiluted latex agglutination slide test for the detection of anti-nucle
A rapid undiluted latex agglutination slide test for the detection of anti-nucleoprotein serum factors associated with systemic lupus erythematosus (sLE)
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which sever
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which several different reagent areas are affixed
JRE,JIL,JJB,JIN,CDM,JMA,JMT,JIR,CEN,LJX
REFRACTOMETER FOR CLINICAL USE,METHOD, ENZYMATIC, GLUCOSE (URINARY, NON-QUANTITA
REFRACTOMETER FOR CLINICAL USE,METHOD, ENZYMATIC, GLUCOSE (URINARY, NON-QUANTITATIVE),AZO-DYES, COLORIMETRIC, BILIRUBIN & ITS CONJUGATES (URINARY, NON-QUANT.),NITROPRUSSIDE, KETONES (URINARY, NON-QUANT.),DIAZONIUM COLORIMETRY, UROBILINOGEN (URINARY, NON-QUANT.),ACID, ASCORBIC, 2,4-DINITROPHENYLHYDRAZINE (SPECTROPHOTOMETRIC),DIAZO (COLORIMETRIC), NITRITE (URINARY, NON-QUANT),INDICATOR METHOD, PROTEIN OR ALBUMIN (URINARY, NON-QUANT.),DYE-INDICATOR, PH (URINARY, NON-QUANT.),TEST, URINE LEUKOCYTE
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which sever
Urine Reagent Strips (URS) for Urinalysis are firm plastic strips to which several different reagent areas are affixed
JIO,JIR,LJX,JMT,JIL
BLOOD, OCCULT, COLORIMETRIC, IN URINE,INDICATOR METHOD, PROTEIN OR ALBUMIN (URIN
BLOOD, OCCULT, COLORIMETRIC, IN URINE,INDICATOR METHOD, PROTEIN OR ALBUMIN (URINARY, NON-QUANT.),TEST, URINE LEUKOCYTE,DIAZO (COLORIMETRIC), NITRITE (URINARY, NON-QUANT),METHOD, ENZYMATIC, GLUCOSE (URINARY, NON-QUANTITATIVE)
A rapid undiluted latex agglutination slide test for the detection of anti-nucle
A rapid undiluted latex agglutination slide test for the detection of anti-nucleoprotein serum factors associated with systemic lupus erythematosus (sLE)
A rapid undiluted latex agglutination slide test for the detection of anti-nucle
A rapid undiluted latex agglutination slide test for the detection of anti-nucleoprotein serum factors associated with systemic lupus erythematosus (sLE)
INTENDED USE For the detection and semi-quantitation of IgG anti-prothrombin (aP
INTENDED USE For the detection and semi-quantitation of IgG anti-prothrombin (aPT) antibodies in individuals with systemic lupus erythematosus (SLE) and lupus-like disorders (e.g., antiphospholipid syndrome). For In Vitro Diagnostic Use.SUMMARY OF THE TEST Antiphospholipid antibodies are a heterogeneous group of immunoglobulins (IgG, IgM, IgA) that bind to several anionic phospholipids (e.g., cardiolipin, phosphatidylserine), to phospholipid-protein complexes, and to certain proteins in the absence of anionic phospholipids. The REAADS aPT ELISA test kit uses purified human prothrombin as antigen to detect IgG anti-prothrombin antibodies in human serum or citrated plasma in the absence of other exogenous cofactors or phospholipids. High serum or plasma levels of aPT antibodies may add valuable information in the laboratory assessment of antiphospholipid antibodies.PRINCIPLE OF THE TEST The test is an indirect ELISA. Diluted serum/citrated plasma samples, calibrators and controls are incubated in microwells coated with purified human prothrombin. After the removal of unbound proteins by washing, antibodies specific for human IgG labeled with horseradish peroxidase (HRP) are added forming complexes with the prothrombin bound antibodies. Following another washing step, the bound enzyme-antibody conjugate is assayed by the addition of a solution containing tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) as the chromogenic substrate. Color develops in the wells. Results are obtained by reading the O.D. of each test well in a spectrophotometer. Calibrator sera are provided with the IgG anti-prothrombin antibody concentration. The user will run a single point calibration, dividing the concentration value of the calibrator sera by the O.D. value of the calibrator providing a conversion factor. The O.D. values of the other samples are multiplied by the conversion factor to obtain IgG anti-prothrombin antibody concentrations in G units. Refer to Product Package Insert.
REAADS IgG Anti-Prothrombin Semi-Quantitative Test Kit
INTENDED USE Detection and semi-quantitation of anti-phosphatidylserine antibodi
INTENDED USE Detection and semi-quantitation of anti-phosphatidylserine antibodies in individuals with systemic lupus erythematosus (SLE) and lupus-like disorders (anti-phospholipid syndrome). For In Vitro Diagnostic Use.SUMMARY AND EXPLANATION OF THE TEST High serum levels of anti-phospholipid antibodies are frequently detected in patients with autoimmune (i.e., SLE) and non-autoimmune diseases, as well as in apparently healthy individuals. These antibodies have been associated with an increased risk for recurrent arterial and venous thrombotic events, thrombocytopenia and fetal loss. Phosphatidylserine is a more physiologically relevant phospholipid due to its presence in cell membranes of endothelial cells and platelets.PRINCIPLE OF THE TESTThe test is an indirect ELISA. Diluted serum/plasma samples, calibrator sera, and controls are incubated in phosphatidylserine coated microwells. β2-glycoprotein I is provided in the sample diluent. After the removal of unbound serum/ plasma proteins by washing, antibodies specific for human IgM, labeled with horseradish peroxidase (HRP), are added forming complexes with the phosphatidylserine bound antibodies. Following another washing step, the bound enzyme-antibody conjugate is assayed by the addition of a single solution containing tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) as the chromogenic substrate. Color develops in the wells at an intensity proportional to the serum concentration of anti-phosphatidylserine (aPS) antibodies. Results are obtained by reading the Optical Density of each well in a spectrophotometer. Calibrator sera are provided with the IgM anti-phosphatidylserine antibody concentrations expressed in MPS (IgM aPS) units traceable to the reference preparations of the Louisville Antiphospholipid Laboratory Control and patient results are determined from the calibration curve. Refer to Package Insert.
Corgenix Anti-Phosphatidylserine IgM Semi-Quantitative Test Kit (192 Well)
INTENDED USE Detection and semi-quantitation of anti-phosphatidylserine antibodi
INTENDED USE Detection and semi-quantitation of anti-phosphatidylserine antibodies in individuals with systemic lupus erythematosus (SLE) and lupus-like disorders (anti-phospholipid syndrome). For In Vitro Diagnostic Use.SUMMARY AND EXPLANATION OF THE TEST High serum levels of anti-phospholipid antibodies are frequently detected in patients with autoimmune (i.e., SLE) and non-autoimmune diseases, as well as in apparently healthy individuals. These antibodies have been associated with an increased risk for recurrent arterial and venous thrombotic events, thrombocytopenia and fetal loss. Phosphatidylserine is a more physiologically relevant phospholipid due to its presence in cell membranes of endothelial cells and platelets.PRINCIPLE OF THE TESTThe test is an indirect ELISA. Diluted serum/plasma samples, calibrator sera, and controls are incubated in phosphatidylserine coated microwells.β2-glycoprotein I is provided in the sample diluent. After the removal of unbound serum/ plasma proteins by washing, antibodies specific for human IgA, labeled with horseradish peroxidase (HRP), are added forming complexes with the phosphatidylserine bound antibodies. Following another washing step, the bound enzyme-antibody conjugate is assayed by the addition of a single solution containing tetramethylbenzidine (TMB) and hydrogen peroxide (H2O2) as the chromogenic substrate. Color develops in the wells at an intensity proportional to the serum concentration of anti-phosphatidylserine (aPS) antibodies. Results are obtained by reading the Optical density of each well in a spectrophotometer. Calibrator sera are provided with the IgA anti-phosphatidylserine antibody concentrations expressed in APS (IgA aPS) units traceable to the reference preparations of the Louisville Antiphospholipid Laboratory Control and patient results are determined from the calibration curve. Refer to Package Insert.
Corgenix Anti-Phosphatidylserine IgA Semi-Quantitative Test Kit (192 Well)