Zebrafish 17 α, 20 β - dihydroxyprogesterone (17 α, 20 β - DHP) ELISA detection kit

Zebrafish 17 α, 20 β - dihydroxyprogesterone (17 α, 20 β - DHP) ELISA detection kitNo separation steps are required, the operation is very simple and fast, and the results can be obtained in a few minutes. When operating the enzyme immunoassay method, all reaction reagents are carried out in the same system. It has been independently developed and sold for many years, and research on ELISA kits has become increasingly professional, ranging from cost to data, helping many researchers complete experiments.

Special operation reminder:

a) The freezing tubes, centrifuge tubes, suction heads used for sampling and storage need to be subjected to high temperature treatment.

b) All sample storage ports must be sealed with sealing film.

c) All sample tube walls need to be clearly labeled with numbers using waterproof markers (for easy identification).

d) All samples should avoid repeated freezing and thawing.

e) If there are any special requirements, please explain them to the sales manager serving the region.

Zebrafish 17 α, 20 β - dihydroxyprogesterone (17 α, 20 β - DHP) ELISA detection kitStore at 2-8 ℃, balance the room temperature for 20 minutes before use, and the concentrated washing solution taken from the refrigerator will crystallize. This is a normal phenomenon. Use it after the crystallization * is dissolved by heating the water bath. The Flat noodles not used in the experiment should be immediately put back into the self sealing bag, sealed (dry at low temperature) for storage. The pretreated sample does not need to be diluted, and 10 μ L can be taken directly for sampling.

Common problem analysis:

1. Reagent selection: Choosing excellent reagents is well-known, but before testing, the reagents should be thawed at room temperature half an hour in advance.

2. Possible issues encountered during sample addition:

3. Easy to cause errors during board washing:

4. Color development issue: Using expired color developers or leaving them for too long after use may cause the color developers to not develop color.

5. Termination reaction: When adding the termination agent, bubbles are generated due to the fast pouring speed, resulting in false positive results. Therefore, the termination agent should be poured slowly.

6. Reading board: When reading the board, the first thing to ensure is that it is clean and tidy.

Disclaimers

1. The reagent kit is for research purposes only and should not be used for clinical or human experiments. Any consequences arising from this shall be borne by the experimenter, and our company shall not be held responsible.

2. Strictly follow the instructions for operation. If the experimenter violates the instructions, the consequences shall be borne by the experimenter.

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