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Purpose
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Enzyme linked immunosorbent assay (ELISA) for the detection of anti-tat IgG in human serum and plasma, as an aid in monitoring the progression of disease in HIV-1 infected patients
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Sample Type
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Serum, Plasma
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Analytical Method
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Quantitative
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Detection Method
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Colorimetric
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Components
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Microtiter strips (12 x 8-well strips) coated with tat protein and blocked with BSA Lysis Buffer: 10ml ready to use, with sodium azide Buffer A (Samples diluent): 50ml ready to use, with preservative Buffer A1 (Positive Control diluent): 1.5ml ready to use, with preservative Buffer B (10X Wash Buffer concentrate): 100ml 10X with preservative, to dilute to 1000 ml final volume with distilled water Buffer S (Secondary Antibody diluent): 20ml ready to use, with preservative Conjugated antibody: goat anti-human IgG-HRP conjugated, 10μl Buffer C: 30ml ABTS Tablets: 2 tablets Buffer C1: 30μl Positive Control: 30μl Negative Control: 10μl
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Material not included
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Microplate reader capable of measuring absorbance at 415 nm Thermomixer, shaking water bath or rocking platform at 37 °C Precision pipettes and pipette tips Glass or plastic pipettes Deionized or distilled water Multi-channel pipette, semi-automated or automated microplate washer 1000 mL graduated cylinder for preparation of 1X Wash Buffer Vortex mixer Glass tubes
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