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Tips: Not for clinical treatment.
Specification: 96T/48T
Mouse Big Endothelin, Big ET ELISA Kit Usage Principle
Operation notes
1 reagent should be stored in the label manual, before using to roomtemperature. The standard after dilute dilute should be discarded, donot save.
2 the experimental plate should be immediately put back in the bag,seal the preservation, lest metamorphism.
3 no other reagents should be packaged or well. Do not mix differentbatches of reagents. Use before the shelf.
4 use a disposable suction head lest cross contamination, draw thetermination liquid and substrate B, a liquid, to avoid using the metalpart of the sample.
5 use clean plastic containers to configure the washing liquid. Allsamples of ingredients and mix well before use in the kit.
6 wash the enzyme plate should be fully dry, do not absorb water paperdirectly into the enzyme labeled pores in the water absorption.
7 substrate a should be volatile, to avoid prolonged open lid.Substrate B is sensitive to light, avoiding prolonged exposure to light.To avoid contact with hand, toxic. After the experiment, read the ODvalue immediately..
8 add reagents should be consistent in order, to ensure that allreaction plate hole incubation time.
9 to carry out the temperature fertility operation according to the time, the amount and the order of the liquid added in the instruction manual.
Kit performance :
1 the correlation coefficient r value of linear regression and the expected concentration of sample was 0.92 above.
The 2 batch and the batch should be less than 9% and 15% respectively.
Detection range:
1.5 -90 g/ml g/ml
Save condition and its validity:
1 reagent kit preservation: 2-8.
2 validity: 6 months
Mouse large endothelin (BigET) ELISA kit
Mouse Big Endothelin, Big ET ELISA Kit Usage Principle
Mouse Big Endothelin, Big ET ELISA Kit Principle of Mouse Big Endothelin (BigET) ELISA Kit <br>Category: FK-QZ3291
The kit was a solid phasesandwich enzyme-linked immunosorbent assay (ELISA), and the AVPconcentrations of the standard samples and unknown concentrations of sampless were detected by the addition of microporous enzyme plates.. Atthe same time, the AVP and the biotin labeled antibodies were incubatedat After washing, the addition of Pro labeled HRP. After the warming and washing, the removal of the non binding enzyme conjugate, and then added to the substrate a, B, and the enzyme conjugate at the same time. Produce color. Color depth and theconcentration of AVP in the sample was proportional to the concentrationof the sample..