HRP-IgG CONJUGATION KIT
PRODUCT DETAILS – HRP-IgG CONJUGATION KIT
- Liquid-based reagents – No reconstitution, just mix and go!
- Sufficient activated HRP to conjugate all IgG at a 4:1 HRP:IgG ratio or optimize ratio to meet your needs.
- Highly efficient HRP incorporation; purification not usually necessary.
- Completely scaleable – Conjugate anywhere from 0.1 to 1 gram IgG per reaction. One chemistry for small-scale development or large-scale manufacturing.
- Conjugates have greatly improved stability compared to other chemistries.
- Shelf life of 24 to 48 months.
- No license needed for commercial use.
BACKGROUND
Enzymes have been used as detection probes for many years and are still commonly used, despite the introduction of fluorescent probes, because of their simplicity, sensitivity and broad-spectrum applications. Enzyme probes, including horseradish peroxidase (HRP) and alkaline phosphatase (AP), are used to detect target proteins through chromogenic, chemiluminescent or fluorescent outputs. HRP is widely used as an enzymatic label in immunochemistry assays. Preparing stable and reproducible antibody-HRP conjugates is one of the biggest challenges of developing immunoassays. The HRP-IgG conjugation kit utilizes a highly robust chemistry to generate highly reproducible IgG-HRP conjugates with a simple procedure. The resulting conjugates have been shown to be extremely stable, retaining 94% activity after storage for 95 days at 37º when stored at a concentration of 0.5 µg/mL. Conjugates are suitable for use on various Immunoassay such as ELISA, Flow Cytometry and Multiplexing platforms such as Luminex. For example, HRP conjugated antibodies have been used in ELISA for testing clinical serum samples for the presence of Dengue virus NS1 (Lai et al., 2019).
REFERENCES
- Lai et al. (2019). Development of an Enzyme-Linked Immunosorbent Assay for Rapid Detection of Dengue Virus (DENV) NS1 and Differentiation of DENV Serotypes during Early Infection. J Clin Microbiol 57:e00221-19.
