The secondary antibodies of the anti-subtype have no crossover with other subtypes of the species, such as anti-mouse IgG2a, anti-mouse IgG2b, anti-mouse IgG1, anti-mouse IgG3, anti-mouse IgA, and anti-mouse IgM. However, we have not conducted any tests on whether there is cross-reaction with subtypes of other species. Our secondary antibodies are specific within the same species range and can rule out cross-reaction issues. If you need secondary antibodies to rule out cross-reactions between different species, you can contact us for personalized customization

The labeled antibodies are recommended to be stored away from light. We will provide light-proof packaging bags when they are dispatched from the warehouse. Customers can subsequently wrap it with aluminum film or place it on the inside of the refrigerator and continue to store it away from light. The reason why we have changed to transparent tube packaging is that customers can see the volume of the contents.

The scope of experiments that the product can be used for should still be subject to the product description on the official website. If it is not written on the official website, it is uncertain whether it can be conducted. Although Elisa experiments have been conducted during the antibody preparation process, there may be structural differences between the antigen on the plate and the antigen used in the experiment. Antigens may also be in the form of polypeptides, etc. Therefore, even if Elisa was conducted during the antibody screening process, it does not mean that the final product is suitable for Elisa experiments on customer samples.

One tablet, approximately 100-200 μ l in dosage. The secondary antibody is used for IHC experiments, with a dilution ratio of about 1:200-1:500, which is roughly 0.2ml

The products are aseptically portioning in the laminar flow hood and contain Proclin preservative

HRP was labeled with 1mg/ml antibody, and the concentration range of the antibody in the final product was 0.8-1.2mg/ml (the mass of HRP labeled on the antibody was not calculated).

Due to the variation in the number of HRP labeled on different antibodies (averaging 2-3, or possibly 1), the extinction coefficient was not determined