|1.0 mg/mL of rabbit anti-HSP27 monoclonal antibody, Dilute to a working concentration of 1 μg/mL in CBS before coating. (Catalog: # 10351-R017)|
|0.5 mg/mL mouse anti-HSP27 monoclonal antibody conjugated to horseradish-peroxidase (HRP). Dilute to working concentration of 0.25 μg/mL in detection antibody dilution buffer before use. (Catalog: # 10351-MM01)|
|Each vial contains 13 ng of recombinant HSP27. Reconstitute with 1 mL detection antibody dilution buffer. After reconstitution, store at -20℃ to -80℃ in a manual defrost freezer. A seven-point standard curve usi ng 2-fold serial dilutions in sample dilution buffer, and a high standard of 0.6 ng/mL is recommended.|
|The minimum detectable dose of Human HSP27 was determined to be approximately 9.4 pg/ml. This is defined as at least three times standard deviations above the mean optical density of 10 replicates of the zero standard.|
|The Human HSP27 ELISA Pair Set is for the quantitative determination of Human HSP27.|
This ELISA Pair Set contains the basic components required for the development of sandwich ELISAs.
The Sino Biological ELISA Pair Set is a solid phase sandwich ELISA (Enzyme-Linked Immunosorbent Assay). It utilizes a monoclonal antibody specific for HSP27 coated on a 96-well plate. Standards and samples are added to the wells, and any HSP27 present binds to the immobilized antibody. The wells are washed and a horseradish peroxidase conjugated mouse anti-HSP27 monoclonal antibody is then added, producing an antibody-antigen-antibody "sandwich". The wells are again washed and TMB substrate solution is loaded, which produces color in proportion to the amount of HSP27 present in the sample. To end the enzyme reaction, the stop solution is added and absorbances of the microwell are read at 450 nm.