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The marker to be labeled needs to have a free primary amine or N-terminal, and the sample must not contain Tris, glycerol, proteins with amino groups or reagents.
The principle of the biotin labeling kit is that the ester bond of the activated biotin and the amino group on the labeled material are dehydrated and condensed to form a stable amide bond. In addition, the N-terminal end of the protein can also be labeled. If there is a primary amine on the protein, such as lysine is what can be labeled.
The detection range of the kit is not equivalent to the concentration range of the sample to be tested. It is recommended to estimate the concentration of the sample to be tested from the relevant literature and to determine the actual concentration of the sample through pre-testing before the experiment. For routine sample types, consult ELISA technical support for recommended dilutions and schedule a pre-test.
If the concentration of the analyte in the sample is too high or too low, dilute or concentrate the sample appropriately. If the analyte concentration in the sample is well below the minimum detection line of the kit, it is recommended to select a more sensitive kit for the assay.
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