Product Introduction:

This product is suitable for protein loading in Tricine-SDS-PAGE electrophoresis. Its main components are SDS, DTT, Coomasi bright blue, buffer salt solution and so on. SDS can combine with proteins to make the protein-SDS complex with a large amount of negative charge. At this time, the charge of the protein itself is completely covered by SDS, eliminating the difference in the charge of various proteins. SDS can also break the intramolecular and intermolecular hydrogen bonds and destroy the secondary and tertiary structures of protein molecules. DTT can break disulfide bonds between cysteine residues, destroying protein structures and eliminating differences between protein structures. Ultimately no charge and structural differences in the protein (subunit), electrophoresis speed is only related to the size of its molecular weight. Coomassie brilliant Blue is used as an indicator during electrophoresis, indicating roughly when the electrophoresis will end.

Instruction:

1. Please add 20 μl buffer for every 20 μl protein sample. If the protein concentration is too high, it can be diluted with double steaming water.

2. After mixing, heat in 100℃ water bath for 5-10 minutes to denature the protein.

3. Cool to room temperature, centrifuge for a few seconds, mix well and then centrifuge for 30 seconds, take the supernatant directly onto the sample.

Note:

This reagent contains DTT, has a certain toxicity, for your safety and health, please wear a laboratory coat and wear disposable gloves operation.

Note：Product information may be optimized and upgraded. Please refer to the actual label information for accuracy.