ELISA test kit guide

ELISA test kit guide

step common problem solution
Experimental preparation 1 The sampler is inaccurate; especially the sampler below 10 ul has a great impact on the results;
2 poor thermal insulation equipment;
3 Washing water is not standardized.
1 calibration sampler; the following 10 ul sampler is best to use imported products (Finland, France, etc.);
2 Carefully adjust the temperature to 37 ° C, the water bath is better;
3 Deionized water or distilled water must be used, and tap water, mineral water, etc. must not be used.
4 Read the instruction manual carefully.
Sample loading 1 The sample is not accurate;
2 No mixing.
1 Be careful when loading the sample. After loading, check again to prevent leakage and mis-addition.
2 After the sample is added, the mixture is repeatedly sucked 3 times to prevent the serum from collecting at the bottom of the well, resulting in non-specific adsorption.
washing Incomplete washing 1 Each time the water is washed, it should be still for 30 seconds;
2 Use absorbent paper as the liner, and buckle the moisture in the dry hole after each washing;
3 Plastic washing bottles are available.
Enzyme reaction Missing After the drop, carefully check each hole
Result judgment 1 Including negative control wells, the color development of each well is generally deep;
2 There is no coloration in each well including the positive control;
3 The positive control did not develop color, while the other samples showed normal color;
4 Some specimens are not dark in color and it is difficult to judge positive.
1 may be insufficient washing; excessive loading; excessive incubation time is too high; follow the instructions to re-operate. If there is no improvement, you can contact the manufacturer;
2 It may be that the sample or enzyme solution is missing; the incubation time is too short and the temperature is too low; the activity of improper storage of the reagent is decreased; follow the instructions. If there is no improvement, you can contact the manufacturer;
3 Positive control missed, added or failed. Re-operate. If there is no improvement, you can contact the manufacturer and ask for the reference product;
4 Re-operate. It is best to use a microplate reader to measure the light absorbance and judge according to the P/N value standard.
Reagent preservation Not standardized Always store at 2-8 °C. Do not be too high or frozen (the enzyme solution will fail after cryopreservation).
Reference substance The lyophilized product According to the control tube, add the corresponding volume of deionized water or distilled water to reconstitute, fully dissolve and mix. Can be used according to the instructions.
other 1 If you have any comments or suggestions on the reagents, please feel free to contact us by phone, email, internet, etc. We will definitely provide a warm service. Thanks a lot!
2 The above mentioned equipment, our company also has supply, if necessary, welcome to consult Jingmei Biological to order.

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