CN101162190A - Method for embedding biological specimen with high water content - Google Patents

Method for embedding biological specimen with high water content Download PDF

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Publication number
CN101162190A
CN101162190A CN 200710093019 CN200710093019A CN101162190A CN 101162190 A CN101162190 A CN 101162190A CN 200710093019 CN200710093019 CN 200710093019 CN 200710093019 A CN200710093019 A CN 200710093019A CN 101162190 A CN101162190 A CN 101162190A
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CN
China
Prior art keywords
sample
embedding
polyglycol
lauxite
specimen
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Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 200710093019
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Chinese (zh)
Inventor
唐安科
唐发辉
赵元莙
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Chongqing Normal University
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Chongqing Normal University
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Publication date
Application filed by Chongqing Normal University filed Critical Chongqing Normal University
Priority to CN 200710093019 priority Critical patent/CN101162190A/en
Publication of CN101162190A publication Critical patent/CN101162190A/en
Pending legal-status Critical Current

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Abstract

The invention relates to an encapsulating method for a biological specimen. The technical proposal adopted is that: a biological specimen is fixed, sterilized, antisepticised and cleaned, polyoxyethylene (PEG six hundred) is used to plasticize the specimen, the plasticized specimen is placed in a porcelain dish which is provided with absorbent paper, is then put into an incubator of thirty degrees to forty degrees for twelve to twenty-four hours and are finally fully integrated with a prepared transparent Lauxite until the preparation of specimen is completed. The encapsulating method has the advantages of a good encapsulating effect, mould proofing, insect prevention and color retention, which is particularly applicable to encapsulating the biological specimen with more water content, such as Craspedacusta, earthworms, mollusks and small-sized fishes.

Description

Embedding method to the more biological sample of water cut
Technical field
The present invention relates to the embedding method of biological sample, particularly to the embedding method of the more biological sample of water cut.
Background technology
Present existing technology mainly is confined to small insects and small-sized plant with transparent Lauxite embedding biological sample, for the many biological samples of cylinder water content, as without special processing, can not be used for embedding.
Summary of the invention
The present invention is directed to the deficiency of existing embedding techniques, the method for the many biological samples of a kind of embedding water cut is provided, concrete technical scheme is as follows:
A kind of embedding method to the more biological sample of water cut is characterized in that carrying out according to the following steps:
(1) biological sample of gathering is fixed, sterilization, anticorrosion, clean, plastify with polyglycol;
(2) take out with the sample after the polyglycol plasticizing and also put it in the porcelain dish that is placed with thieving paper, go to place after 12~24 hours in 30~40 ℃ of incubators standby;
(3) biological sample of getting after the plasticizing of the transparent Lauxite for preparing and polyglycol is integrated into this embedding of rower fully: add transparent Lauxite and make primer in plastic containers, treat to put into after it solidifies the sample of step (2) gained, and insert sample with insect needle or stainless steel wire and fix, slowly add transparent Lauxite up to sample is covered embedding fully, treat to add once more after it solidifies transparent Lauxite and make to bind glue, this moment rotatable insect needle and pin taken out; After treating the complete setting and hardening of Lauxite, take out products made thereby.
Step (2) gained sample is drawn with thieving paper before embedding again, to remove the unnecessary polyglycol in sample surface.
Preferably using molecular weight in the plasticizing process is 600 polyglycol.
The described plasticizing process of step (1) is Chinese invention patent 200510020434.9 disclosed plasticizing methods.
The present invention compared with the prior art, difference is sample to be plastified with polyglycol before the embedding, so not only can keep the original attitude of sample in good condition, also can and colloid between well merge, phenomenon can not occur peeling off, and colloid itself also can keep pellucidity.
The present invention can remedy the deficiency of existing embedding techniques, and the many biological samples of energy embedding water cut are as craspedacusta sowerbyi, earthworm, mollusc, small fishes etc.; And this method embedding effect is better, has advantages such as mildew-resistant, insect protected, guarantor's look.
Specific embodiment
The embedding of craspedacusta sowerbyi sample
(1) craspedacusta sowerbyi is fixed, sterilization, anticorrosion; Clean: the sample that will be dipped in the antiseptic takes out, and washes repeatedly with clear water antiseptic is removed; Plasticizing: working concentration gradient molecular weight from low to high be 600 polyglycol as plasticiser, sample is plastified, so that polyglycol is replaced out the moisture in the sample fully;
(2) sample that takes out after the polyglycol plasticizing also puts it in the porcelain dish that is placed with thieving paper, goes in 30~40 ℃ of incubators and places 12~24 hours, to finish the processing of sample before the embedding;
(3) biological sample of getting after the transparent Lauxite for preparing and the plasticizing merges fully: add transparent Lauxite and make primer, treat to put into after it solidifies the sample of step (2) gained, and insert sample with insect needle or stainless steel wire and fix, slowly add transparent Lauxite up to sample is covered embedding fully, add transparent Lauxite once more and make to bind glue, this moment rotatable insect needle or stainless steel wire and with its taking-up.Finish until technology.

Claims (2)

1. embedding method to the more biological sample of water cut is characterized in that carrying out according to the following steps:
(1) biological sample of gathering is fixed, sterilization, anticorrosion, clean, plastify with polyglycol;
(2) take out with the sample after the polyglycol plasticizing and also put it in the porcelain dish that is placed with thieving paper, go to place after 12~24 hours in 30~40 ℃ of incubators standby;
(3) biological sample of getting after the plasticizing of the transparent Lauxite for preparing and polyglycol is integrated into this embedding of rower fully: add transparent Lauxite and make primer in plastic containers, treat to put into after it solidifies the sample of step (2) gained, and insert sample with insect needle or stainless steel wire and carry out with fixed, slowly add transparent Lauxite up to sample is covered embedding fully, treat to add once more after it solidifies transparent Lauxite and make to bind glue, this moment rotatable insect needle and pin taken out; After treating the complete setting and hardening of Lauxite, take out products made thereby.
2. according to claim 1 to the embedding method of the more biological sample of water cut, it is characterized in that: the molecular weight of described polyglycol is 600.
CN 200710093019 2007-11-22 2007-11-22 Method for embedding biological specimen with high water content Pending CN101162190A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200710093019 CN101162190A (en) 2007-11-22 2007-11-22 Method for embedding biological specimen with high water content

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200710093019 CN101162190A (en) 2007-11-22 2007-11-22 Method for embedding biological specimen with high water content

Publications (1)

Publication Number Publication Date
CN101162190A true CN101162190A (en) 2008-04-16

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CN (1) CN101162190A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103115809A (en) * 2013-01-23 2013-05-22 浙江大学 Transmission electron microscope processing method for insect antenna samples
CN103814890A (en) * 2014-03-26 2014-05-28 青岛大学 Method for making large helminth specimen
CN104996397A (en) * 2015-07-03 2015-10-28 陕西省微生物研究所 Macrofungi specimen preparation method
CN105010302A (en) * 2015-07-08 2015-11-04 南宁千年工艺有限公司 Method for preparing resin-embedded water-containing animal specimen
CN104392653B (en) * 2014-12-19 2016-08-17 陈军凤 The method for shaping of piscine organism sample
CN107183002A (en) * 2017-05-10 2017-09-22 广西柳州中嘉知识产权服务有限公司 Butterfly specimen preparation method
CN108871899A (en) * 2018-07-12 2018-11-23 泰山医学院 Microsection manufacture method for histocyte dyeing

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103115809A (en) * 2013-01-23 2013-05-22 浙江大学 Transmission electron microscope processing method for insect antenna samples
CN103115809B (en) * 2013-01-23 2016-04-27 浙江大学 A kind of sample for use in transmitted electron microscope disposal route of insect feeler
CN103814890A (en) * 2014-03-26 2014-05-28 青岛大学 Method for making large helminth specimen
CN104392653B (en) * 2014-12-19 2016-08-17 陈军凤 The method for shaping of piscine organism sample
CN104996397A (en) * 2015-07-03 2015-10-28 陕西省微生物研究所 Macrofungi specimen preparation method
CN105010302A (en) * 2015-07-08 2015-11-04 南宁千年工艺有限公司 Method for preparing resin-embedded water-containing animal specimen
CN107183002A (en) * 2017-05-10 2017-09-22 广西柳州中嘉知识产权服务有限公司 Butterfly specimen preparation method
CN108871899A (en) * 2018-07-12 2018-11-23 泰山医学院 Microsection manufacture method for histocyte dyeing

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Open date: 20080416