Routine paraffin wax flaking HE dyeing non-xylol whole-course treatment liquid for biological organization sample
A biological tissue and xylene technology, applied in the field of in vitro diagnostic reagents, can solve problems such as waste of resources, complicated operation, lack of uniform standards, etc., and achieve the effect of stable use, simple and fast operation, and easy mastery
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Embodiment 1
[0041] The tissue fixative set number of the conventional paraffin-waxed HE staining and xylene-free full treatment solution of the biological tissue sample of the present invention is the first tank, the tissue dehydrating solution I is the second tank, and the tissue dehydrating solution II is the third tank. The transparent liquid is the fourth tank, the tissue wax solution I is the fifth tank, and the tissue wax solution II is the sixth tank. When biological tissue samples are dehydrated, the biological tissue samples are put into the first to sixth tanks in sequence. The operation requirements are as follows:
[0042] Putting into the first tank: 16:00 to 19:30 that day; (Soaking time: 3 hours and 30 minutes)
[0043] Time to put in the second tank; 19:30 to 21:00 that night; (Soaking time: 1 hour 30 minutes)
[0044] Time to put in the third tank: 21:30 to 22:30 that day; (Soaking time: 1 hour 30 minutes)
[0045] Putting into the fourth tank: 22:30 in the evening of the sam...
Embodiment 2
[0050]The section dewaxing solution I described in the general treatment solution for HE staining of conventional paraffin slices of biological tissue samples of the present invention without xylene is the seventh tank, the section dewaxing solution II is the eighth tank, and the hematoxylin staining solution is the ninth tank. , Eosin staining solution is the tenth tank, the de-floating solution is the eleventh tank, the dewatering clear solution is the twelfth tank, and the slice clear solution is the thirteenth tank.
[0051] The following is the staining process of biological tissue sample sections:
[0052] (1) Put the biological tissue sample slice into the seventh tank and soak for five minutes, then take it out and put it in the eighth tank.
[0053] (2) Immerse the biological tissue sample slice in the eighth tank for five minutes and take it out;
[0054] (3) Wash the biological tissue sample section with tap water for two minutes, then put it in the ninth tank, soak in ...
Embodiment 3
[0059] Procedure requirements for HE staining of large and small tissue sections:
[0060] (1) The HE staining method and time of large tissue and micro tissue sections are the same. The frosted part of the slide can only be marked with a 2B pencil, otherwise the writing will be difficult to retain. When the room temperature is above 15°C, the wax block should be cooled on ice to prevent the wrinkles from opening and sectioning. The thickness of the tissue section is 3 to 4 μm, and the wrinkles are fully opened.
[0061] (2) How to use the anti-slipping solution: mainly used for blood clots and tissue slices that are easy to peel off. Each slice should be placed on the appropriate position of the slide with very little solution, and another slide can be attached and opened. Can be used, or wipe off excess anti-dropping tablets with your fingers.
[0062] (3) Drying treatment: The prepared tissue sections are dried in a wax melting incubator or in a dryer for 20 to 30 minutes.
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