Human RIPK3 ELISA Kit Enzymes and Regulators dual-wavelength detection was performed using

dual-wavelength detection was performed using a microplate reader to determine 450nm Absorption maximum wavelength and 570nm Or 630nm At reference wavelength OD Value

Theory Based on the caspase 2 specific hydrolysis of peptide substrate Ac-VDQQD-pNA (Val Asp Val Ala Asp p nitroanilide)

01 mmol/L - 1 mmol/L Applications Used for the detection and quantification of Phytase activity

Ferritin heavy chain

Human RIPK3 ELISA Kit Enzymes and Regulators dual-wavelength detection was performed usingProduct Specification Usage Required experimental equipment: 1. Microplate reader (450nm) 2. High precision pipettes and pipette tips: 0. 5 10uL, 5 50uL, 20 200uL, 200 1000uL 3. 37C incubator 4. Distilled or deionized water Sample preparation and requirements: Tissue homogenization: Rinse the tissue with pre chilled PBS (0. 01M, pH 7. 4) to remove residual blood (lysed red blood cells in the homogenate will affect the measurement results). Weigh and