生物活性 | |||
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描述 | In the realm of enzyme-linked immunosorbent assay (ELISA), a micro-technique utilizing ABTS as a substrate for horseradish peroxidase (HRP) conjugate has been evaluated. Among four compared substrates—5-aminosalicylic acid (5AS), O-phenylenediamine (OPD), O-tolidine (OT), and ABTS-ABTS shines for its sensitivity, stability, and distinctive bluish-green color, enhancing its visual detectability in assays[1]. ABTS, a commonly employed peroxidase substrate, is pivotal for the large-scale cultivation and subsequent analysis of peroxidase-positive transformants, aiming at the production of active protein. Notably, after 160 hours of cultivation, an activity peak of 55,000 U/L is recorded in the presence of ABTS, highlighting the enzyme's optimal performance with this substrate. The activity notably diminishes as H2O2 concentration exceeds 0.125 mM, illustrating the enzyme's susceptibility to inhibition by H2O2, with the maximum reaction rates achieved varying based on the substrate, ranging from 31.2 to 125 μM[2]. |
实验方案 | |||
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1mg | 5mg | 10mg | |
1 mM 5 mM 10 mM |
1.82mL 0.36mL 0.18mL |
9.11mL 1.82mL 0.91mL |
18.23mL 3.65mL 1.82mL |
参考文献 |
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