CN106980018A - A kind of kit of application CD45 immunofluorescences joint CEP17 probe identification circulating tumor cells and its application - Google Patents
A kind of kit of application CD45 immunofluorescences joint CEP17 probe identification circulating tumor cells and its application Download PDFInfo
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Abstract
The invention belongs to biomedical clinical detection field, and in particular to a kind of application CD45 immunofluorescences joint CEP17 fluorescence in situ hybridization probe one-step method contaminates kit and its application of identification circulating tumor cell altogether.The kit includes:Fixer, 2 × SSC, 40/0.4 × SSC of 0.3%NP, 0.075M KCl solution, CD45 monoclonal antibodies and CEP17 probes mixed liquor, DAPI counterstains, perforation agent, confining liquid and mountant.The circulating tumor cell that the present invention is captured using the joint CEP17 fluorescence in situ hybridization probe identifications of CD45 Immunofluorescent Antibodies, immunofluorescence and fluorescence in situ hybridization detection are completed by one-step method, overcome Immunofluorescence test and exist when fluorescence in situ hybridization detection is used in combination and interfere, detect the problem of taking longer, one-step method hybridization incubation is rapidly completed in 2h, detection time is greatly reduced, and testing result observation is directly perceived.
Description
Technical field
The invention belongs to biomedical clinical detection field, and in particular to one kind application CD45 immunofluorescence joints CEP17
The kit of fluorescence in situ hybridization probe identification circulating tumor cell and its application.
Background technology
Circulating tumor cell (circulating tumor cells, CTCs) refers to be present in all kinds of in peripheral blood
The general designation of tumour cell, because of spontaneous or operation of diagnosis and treatment, from entity tumor focus (primary tumor, transfer stove), coming off discharges into periphery
The tumour cell of blood circulation, most of CTCs occurs apoptosis or swallowed after peripheral blood is entered, and minority can escape and anchor
Develop into transfer stove.Clinical manifestations of the CTCs in terms of diagnosing tumor, treatment and monitoring in recent years is gradually shown up prominently, and is
Current most potential tumour non-invasive diagnosis and real-time curative effect monitoring means, clinical value are extremely notable.With tradition
Imaging diagnosis, endoscopy and pathological diagnosis compare, advantage significantly, can more sensitively find the change of disease
Change, more science, the effect for rapidly evaluating a certain therapeutic scheme.And separation and concentration CTCs need to only extract a small amount of periphery of patient
Blood, is free from side effects to patient, therefore with the monitoring of frequent, can reach the purpose of real-time monitoring of diseases progress.It is even more important
, CTCs can as analysis patient tumors biological property real-time sample, it can be found that patient real-time biological change,
And therapeutic scheme is adjusted according to result in time, realize real-time individualized treatment.
The method of CTCs enrichment captures is substantially based on following three kinds of principles:Immunocapture, cell size, other features
Recognize (such as cell density, electric charge, deformability), first two is to apply more method at present.CTCs is identified after capture
Be realize CTCs apply to clinical tumor patient curative effect assess in real time, the state of an illness is monitored in real time, direction of medication usage and Index for diagnosis
It is crucial.Identification CTCs most common methods mainly have 6 kinds of methods:(1) immunofluorescence technique;(2) flow cytometry;(3) fluorescence is former
Position hybrid method;(4)RT-PCR;(5) gene chips;(6) two generation PCR sequencing PCRs.Immunofluorescence technique and flow cytometry are based on CTCs
Memebrane protein characterization technology;It is special that fluorescence in situ hybridization, RT-PCR, gene chips and two generation PCR sequencing PCRs are based on CTCs nucleic acid
Levy identification technology.
Immunofluorescence is the principle combined using antigen with antibody specificity, fluorescein-labeled antibody is swollen with special
Tumor markers (mainly including epithelial cell keratin, epithelial cell membrane specific antigen etc.) are combined, and pass through enzyme and substrate reactions
Develop the color to judge the presence of tumour cell.Immunofluorescence is to detect CTCs one of maturation method, easy, directly perceived and can carry out
Morphological analysis, but its sensitiveness only has 105Left and right, and the tumour of many differentiation differences can not express target antigen, Er Feishang
Cytokeratin and epithelial antigen also may be positive in chrotoplast, under mirror result is observed in addition and interpretation subjectivity compared with
By force, these all limit application of the immunofluorescence in CTCs detections.
FISH (Fluorescence in situ hybridization, FISH) is an emerging molecule
Cytogenetic techniques, are to grow up on the basis of original radioactive in situ hybridization technology phase late 1980s
A kind of nonradioactivein situhybridization technology.This current technology has been widely used for the structural research of animal-plant gene group, dyeing
The many such as the analysis of variance of body fine structure, viral infection assays, mankind's pre-natal diagnosis, cancer genetics and genome evolution research
Field.FISH general principle is to mark single-chain nucleic acid to be probe with known, according to the principle of base complementrity, with material to be checked
In unknown single-chain nucleic acid specifically bound, form the heteroduplex nucleic acid that can be detected.Because DNA molecular is in chromosome
On be linearly to be arranged along the chromosome longitudinal axis, thus hybridization can be directly carried out with chromosome with probe so as to by specific base
Because positioning on chromosome.Compared with traditional radioactive label in situ hybridization, FISH has quick, detection signal
By force, hybrid specificities are high and can be with multiple staining the features such as, therefore in molecular cytogenetics field by common concern.Fluorescence
Hybridization in situ technique is applied to detection CTCs chromosome polyploids, gene break, during Gene Fusion, due in the CTCs of capture
There is substantial amounts of haemocyte background, under fluorescence microscope, searching target CTCs is extremely difficult, exists so as to limit FISH technology
Application in CTCs.
The content of the invention
The present invention is in view of the shortcomings of the prior art, it is therefore intended that provide a kind of application CD45 immunofluorescences joint CEP17 glimmering
The kit of light in situ hybridization probe identification circulating tumor cell and its application.
For achieving the above object, the technical solution adopted by the present invention is:
A kind of application CD45 immunofluorescences joint CEP17 fluorescence in situ hybridization probe identifies the reagent of circulating tumor cell
Box, including:Fixer, 2 × SSC, 0.3%NP-40/0.4 × SSC, 0.075M KCl solution, CD45 monoclonal antibodies and CEP17 probes
Mixed liquor, DAPI counterstains, perforation agent, confining liquid and mountant.
In such scheme, the component of CD45 monoclonal antibodies and CEP17 the probe mixed liquor is fluorescence labeling CD45 monoclonal antibodies,
CEP17 fluorescence in situ hybridization probe, dextran sulfate, deionized formamide, BSA, SSC, Triton-100.
In such scheme, the concentration of CD45 monoclonal antibodies and CEP17 probe the mixed liquor each component is:Fluorescence labeling CD45 is mono-
Anti- concentration is 0.002mg/ml, and the concentration of CEP17 fluorescence in situ hybridization probe is 2ng/ μ the L, (quality of dextran sulfate 10%
Concentration), deionized formamide 50% (volumetric concentration), BSA1% (mass concentration), 6 × SSC, (the volumes of Triton-100 1 ‰
Concentration).
In such scheme, the fixer is methanol and glacial acetic acid by volume 3:1 mixing gained mixed liquor.
In such scheme, the component of the perforation agent is 5 ‰ Triton X-100,0.1M phosphate buffers.
In such scheme, the component of the confining liquid is 5% BSA.
In such scheme, the mountant is resin.
Mentioned reagent box is preparing the application in being used to identify circulating tumor cell product, specifically comprises the following steps:
(1) harvesting:The circulating tumor cell sample (CTCs) of capture is drawn to conical centrifuge tube, centrifuges, remove supernatant;
(2) it is hypotonic:0.075mol/L KCl 6~8mL of solution of pre-temperature to 37 DEG C are added, rearmounted 37 are mixed with suction pipe piping and druming
DEG C 20~30min of incubator;
(3) pre-fix:Fixer 2mL is added, piping and druming is mixed, centrifugation;
(4) suck supernatant, plus Fresh fixer 5mL, piping and druming mixes, fixed 10min, centrifugation;
(5) repeat step (4) is until cell precipitation whitens wash clean;
(6) preparation of cell suspension:Supernatant is sucked, appropriate fixer is added, the suitable cell suspension (10 of concentration is made
× object lens observe cell density under phase contrast microscope, it is desirable to which cell is non-overlapping, and the wild cell quantity of haplopia is at 100~200
It is advisable);
(7) film-making:Draw 3~5 μ L cell suspensions to drop on anticreep slide, 56 DEG C of agings 0.5~2 hour;
(8) close:Added to slide after 100ul confining liquids, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(9) perforate:It is added dropwise after 100ul perforation agent, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(10) it is dehydrated:Slide is sequentially placed into 70Vt% (volumetric concentration) ethanol, 85Vt% ethanol and 100Vt% ethanol
Slide is spontaneously dried after each 2min dehydrations;
(11) hybridization incubation:CD45 monoclonal antibodies and CEP17 probe mixed liquors are taken out, is stored at room temperature 5 minutes, it is short after thoroughly mixing
Temporarily centrifugation, takes 10 μ L drops in cell drop piece hybridising region, 22mm × 22mm cover glass is covered immediately, probe should under cover glass
Uniform expansion bubble-free, uses resin edge sealing, slide is placed on hybridization instrument and carries out hybridization incubation;
(12) wash:The slide after being incubated is taken out, the rubber glue on cover glass is removed, slide is placed in 65 DEG C~68 immediately
In DEG C 0.3%NP-40/0.4 × SSC solution, 10~20s of vibration sloughs cover glass, soaks 5~10 minutes, slide is placed in into 37
In DEG C deionized water, 1~3s is vibrated, is soaked 2 minutes, dark place spontaneously dries slide;
(13) mounting:10ul DAPI counterstains are added dropwise;
(14) diagosis:Under fluorescence microscope slide is observed from suitable optical filter;
(15) result judgement:A.CD45 stained positives are leucocyte;B.CD45 is not colored, but is non-in huge bare nucleus
Tumour cell;C.CD45 is not colored, signaling point >=2, and non-huge bare nucleus may determine that as circulating tumor cell, be counted
Number.
In such scheme, the condition of step (11) described hybridization incubation is:75 DEG C are denatured 2 minutes, and 37 DEG C are incubated 2 hours.
Beneficial effects of the present invention are as follows:
(1) present invention is overcome immune using immunofluorescence joint fluorescence in situ hybridization technique identification circulating tumor cell
When fluoroscopic examination or the detection of fluorescence in situ hybridization detection monotechnics, testing result can not fully turn out to be circulating tumor cell
Shortcoming, reduces the mistake of circulating tumor cell identification;
(2) circulation that the present invention is captured using the joint CEP17 fluorescence in situ hybridization probe identifications of CD45 Immunofluorescent Antibodies
Tumour cell, immunofluorescence and fluorescence in situ hybridization detection are completed by one-step method, and one-step method hybridization incubation is quick in 2h
Complete, greatly reduce detection time;
(3) heretofore described CEP17 probes are prepared from using non repetitive sequence technology, are reduced conventional CEP17 and are visited
Pin can effectively reduce the miscount of circulating tumor cell because of nonspecific hybridization signals caused by repetitive sequence;Simultaneously should
CEP17 probes prepared by technology can be rapidly completed hybridization within 2 hours, when 16~24 hours than conventional probe hybridize
Between, greatly shorten.
Brief description of the drawings
Fig. 1 is the circulating tumor that this kit identifies capture, and wherein A cells are not by CD45 red colourations, while containing in core
Multiple (> 2) FISH signals, the cell is circulating tumor cell;B cell contains 2 by CD45 red colourations in core
Individual fluorescence signal point, the cell is blood cell (leucocyte).
Fig. 2 is the circulating tumor that this kit identifies capture, and wherein A cells are not by CD45 red colourations, while containing 2 in core
Individual FISH signal, the cell is circulating tumor cell, the multiple tumour cell formation bulks of the sample.
Fig. 3 is the circulating tumor that this kit identifies capture, and wherein A cells are not by CD45 red colourations, while containing in core
Multiple (> 2) FISH signals, the cell is circulating tumor cell;B cell contains 2 by CD45 red colourations in core
Individual fluorescence signal point, the cell is blood cell (leucocyte).
Embodiment
For a better understanding of the present invention, with reference to the embodiment content that the present invention is furture elucidated, but the present invention
Content is not limited solely to the following examples.
Embodiment 1
A kind of application CD45 immunofluorescences joint CEP17 fluorescence in situ hybridization probe identifies the reagent of circulating tumor cell
Box, the composition of kit is as shown in table 1 below:
The kit forms of table 1
Embodiment 2
Patient with breast cancer's circulating tumor cell ,+No. 17 dyes of CD45 monoclonal antibodies of use are identified using kit described in embodiment 1
Colour solid fluorescence in situ hybridization probe detects that No. 17 chromosome fluorescence in-situ hybridization probe-specific sequences (SEQ ID NO.1) are:
TGAACATTCCTTTGGATGGAGCAGGTTTGAGACACTCTTTTTGTACAATCTACAAGTGGATATTTGGACCTCTCTGA
GGATTTCGTTGGAAACGGGATAACTGCACCTAACTAAACGGAAGCATTCTCAGAAACTTCTTGGTGATGTTTGCATT
CAAATCCCAGAGT
Specifically include following steps:
(1) harvesting:The circulating tumor cell sample (CTCs) of capture is drawn to conical centrifuge tube, centrifuged, 1000 turns/
Min, 10min, remove supernatant;
(2) it is hypotonic:0.075mol/L KCL 6~8mL of solution of pre-temperature to 37 DEG C are added, rearmounted 37 are mixed with suction pipe piping and druming
DEG C 20~30min of incubator;
(3) pre-fix:Fixer 2mL is added, piping and druming is mixed, 1000 turns/min centrifugations 10min;
(4) suck supernatant, plus Fresh fixer 5mL, piping and druming mixes, fixed 10min, 1000 turns/min centrifugations
10min;
(5) repeat step (4) is until cell precipitation whitens wash clean;
(6) preparation of cell suspension:Supernatant is sucked, appropriate fixer is added, the suitable cell suspension of concentration is made;
(7) film-making:Draw 3~5 μ L cell suspensions to drop on anticreep slide, 56 DEG C of agings 0.5~2 hour;
(8) close:Added to slide after 100ul confining liquids, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(9) perforate:It is added dropwise after 100ul perforation agent, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(10) it is dehydrated:Slide is sequentially placed into each 2min dehydrations in 70Vt% ethanol, 85Vt% ethanol and 100Vt% ethanol
After spontaneously dry slide;
(11) hybridization incubation:CD45 monoclonal antibodies and CEP17 probe mixed liquors are taken out, is stored at room temperature 5 minutes, it is short after thoroughly mixing
Temporarily centrifugation, takes 10 μ L drops in cell drop piece hybridising region, 22mm × 22mm cover glass is covered immediately, probe should under cover glass
Uniform expansion bubble-free, uses resin edge sealing, slide is placed on hybridization instrument, and 75 DEG C are denatured 2 minutes, and 37 DEG C are incubated 2 hours;
(12) wash:The slide after being incubated is taken out, the rubber glue on cover glass is removed, slide is placed in 65 DEG C~68 immediately
In DEG C 0.3%NP-40/0.4 × SSC solution, cover glass is sloughed in vibration for 10~20 seconds, soaks 5~10 minutes, slide is placed in into 37
In DEG C deionized water, vibrate 1~3 second, soak 2 minutes, dark place spontaneously dries slide;
(13) mounting:10ul DAPI counterstains are added dropwise;
(14) diagosis:Under fluorescence microscope slide is observed from suitable optical filter.
Testing result as depicted in figs. 1 and 2, Fig. 1 be this kit identify capture circulating tumor, wherein A cells not by
CD45 red colourations, while containing multiple (> 2) FISH signals in core, the cell is circulating tumor cell;B is thin
Born of the same parents are by CD45 red colourations, containing 2 fluorescence signal points in core, and the cell is blood cell (leucocyte).
Fig. 2 is the circulating tumor that this kit identifies capture, and wherein A cells are not by CD45 red colourations, while containing 2 in core
Individual FISH signal, the cell is circulating tumor cell, the multiple tumour cell formation bulks of the sample.
Embodiment 3
Using kit described in the embodiment of the present invention, examined using CD45 immunofluorescences and CEP17 FISHs joint
Patients with gastric cancer circulating tumor cell is surveyed, No. 17 chromosome fluorescence in-situ hybridization probe-specific sequences (SEQ ID NO.1) are:
TGAACATTCCTTTGGATGGAGCAGGTTTGAGACACTCTTTTTGTACAATCTACAAGTGGATATTTGGAC
CTCTCTGAGGATTTCGTTGGAAACGGGATAACTGCACCTAACTAAACGGAAGCATTCTCAGAAACTTCTTGGTGATG
TTTGCATTCAAATCCCAGAGT
Specifically include following steps:
(1) harvesting:Peripheral blood in patients 10ml is extracted, instrument is captured using commercially available circulating tumor cell or kit is caught
The circulating tumor cell (CTCs) obtained, the circulating tumor cell after capture is drawn to conical centrifuge tube, centrifugation, 1000 turns/min,
10min, removes supernatant;
(2) it is hypotonic:0.075mol/LKCL 6~8mL of solution of pre-temperature to 37 DEG C are added, rearmounted 37 are mixed with suction pipe piping and druming
DEG C 20~30min of incubator;
(3) pre-fix:Fixer 2mL is added, piping and druming is mixed, 1000 turns/min centrifugations 10min;
(4) suck supernatant, plus Fresh fixer 5mL, piping and druming mixes, fixed 10min, 1000 turns/min centrifugations
10min;
(5) repeat step (4) is until cell precipitation whitens wash clean;
(6) preparation of cell suspension:Supernatant is sucked, appropriate fixer is added, the suitable cell suspension of concentration is made;
(7) film-making:Draw 3~5 μ L cell suspensions to drop on anticreep slide, 56 DEG C of agings 0.5~2 hour;
(8) close:Added to slide after 100ul confining liquids, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(9) perforate:It is added dropwise after 100ul perforation agent, room temperature closing 10min, 2 × SSC (pH 7.0) rinsings 5min;
(10) it is dehydrated:Slide is sequentially placed into 70% ethanol, 85% ethanol and 100% ethanol natural after each 2min dehydrations
Dry slide;
(11) hybridization incubation:CD45 monoclonal antibodies and CEP17 probe mixed liquors are taken out, is stored at room temperature 5 minutes, it is short after thoroughly mixing
Temporarily centrifugation, takes 10 μ L drops in cell drop piece hybridising region, 22mm × 22mm cover glass is covered immediately, probe should under cover glass
Uniform expansion bubble-free, uses resin edge sealing, slide is placed on hybridization instrument, and 75 DEG C are denatured 2 minutes, and 37 DEG C are incubated 2 hours;
(12) wash:The slide after being incubated is taken out, the rubber glue on cover glass is removed, slide is placed in 65 DEG C~68 immediately
In DEG C 0.3%NP-40/0.4 × SSC solution, cover glass is sloughed in vibration for 10~20 seconds, soaks 5~10 minutes, slide is placed in into 37
In DEG C deionized water, vibrate 1~3 second, soak 2 minutes, dark place spontaneously dries slide;
(13) mounting:10ul DAPI counterstains are added dropwise;
(14) diagosis:Under fluorescence microscope slide is observed from suitable optical filter.
Testing result is as shown in Figure 3.Fig. 3 is the circulating tumor that this kit identifies capture, and wherein A cells are not contaminated by CD45
Red, while containing multiple (> 2) FISH signals in core, the cell is circulating tumor cell;B cell is by CD45
Containing 2 fluorescence signal points in red colouration, core, the cell is blood cell (leucocyte).
Obviously, above-described embodiment is only intended to clearly illustrate made example, and the not limitation to embodiment.It is right
For those of ordinary skill in the art, can also make on the basis of the above description it is other it is various forms of change or
Change.There is no necessity and possibility to exhaust all the enbodiments.And the obvious change or change therefore amplified
Move within still in the protection domain of the invention.
Sequence table
<110>Wuhan Kang Lu Biotechnology Ltd.
<120>A kind of kit of application CD45 immunofluorescences joint probe identification circulating tumor cells of CEP 17 and its application
<160>1
<210> 1
<211> 167bp
<212> DNA
<213>Artificial sequence
<400> 1
tgaacattcc tttggatgga gcaggtttga gacactcttt ttgtacaatc tacaagtgga 60
tatttggacc tctctgagga tttcgttgga aacgggataa ctgcacctaa ctaaacggaa 120
gcattctcag aaacttcttg gtgatgtttg cattcaaatc ccagagt 167
Claims (10)
1. a kind of application CD45 immunofluorescences joint CEP17 fluorescence in situ hybridization probe identifies the kit of circulating tumor cell,
It is characterised in that it includes:Fixer, 2 × SSC, 0.3%NP-40/0.4 × SSC, 0.075M KCl solution, CD45 monoclonal antibodies and
CEP17 probes mixed liquor, DAPI counterstains, perforation agent, confining liquid and mountant.
2. kit according to claim 1, it is characterised in that the component of CD45 monoclonal antibodies and CEP17 the probe mixed liquor
For fluorescence labeling CD45 monoclonal antibodies, CEP17 fluorescence in situ hybridization probe, dextran sulfate, deionized formamide, BSA, SSC and
Triton-100。
3. kit according to claim 2, it is characterised in that CD45 monoclonal antibodies and CEP17 probe the mixed liquor each component
Concentration be:The concentration of fluorescence labeling CD45 monoclonal antibodies is 0.002mg/ml, and the concentration of CEP17 fluorescence in situ hybridization probe is 2ng/
μ L, dextran sulfate 10%, deionized formamide 50%, BSA1%, 6 × SSC, Triton-100 1 ‰.
4. kit according to claim 1, it is characterised in that the fixer is methanol and glacial acetic acid by volume 3:1
Mixing gained mixed liquor.
5. kit according to claim 1, it is characterised in that the component of the perforation agent be 5 ‰ Triton X-100,
0.1M phosphate buffers.
6. kit according to claim 1, it is characterised in that the component of the confining liquid is 5% BSA.
7. kit according to claim 1, it is characterised in that the mountant is resin.
8. any kit of claim 1 ~ 7 is preparing the application in being used to identify circulating tumor cell product.
9. application according to claim 8, it is characterised in that specifically comprise the following steps:
(1)Harvesting:By the circulating tumor cell sample of capture(CTCs)Conical centrifuge tube is drawn to, centrifuges, remove supernatant;
(2)It is hypotonic:0.075mol/L KCl 6 ~ 8mL of solution of pre-temperature to 37 DEG C are added, rearmounted 37 DEG C of perseverances are mixed with suction pipe piping and druming
20 ~ 30min of incubator;
(3)Pre-fix:Fixer 2mL is added, piping and druming is mixed, centrifugation;
(4)Suck supernatant, plus Fresh fixer 5mL, piping and druming mixes, fixed 10min, centrifugation;
(5)Repeat step(4)Until cell precipitation whitens wash clean;
(6)The preparation of cell suspension:Supernatant is sucked, appropriate fixer is added, the suitable cell suspension of concentration is made;
(7)Film-making:Draw 3 ~ 5 μ L cell suspensions to drop on anticreep slide, 56 DEG C of agings 0.5 ~ 2 hour;
(8)Closing:Added to slide after 100uL confining liquids, room temperature closing 10min, 2 × SSC rinsings 5min;
(9)Perforation:It is added dropwise after 100ul perforation agent, room temperature closing 10min, 2 × SSC rinsings 5min;
(10)Dehydration:Slide is sequentially placed into 70%, 85% and 100% ethanol solution after each 2min dehydrations and spontaneously dries slide;
(11)Hybridization incubation:Take out CD45 monoclonal antibodies and CEP17 probe mixed liquors, be stored at room temperature 5 minutes, after thoroughly mixing it is of short duration from
The heart, takes 10 μ L drops in cell drop piece hybridising region, 22mm × 22mm cover glass is covered immediately, probe should be uniform under cover glass
Deploy bubble-free, use resin edge sealing, slide is placed on hybridization instrument and carries out hybridization incubation;
(12)Washing:The slide after being incubated is taken out, the rubber glue on cover glass is removed, slide is placed in 65 DEG C ~ 68 DEG C immediately
In 0.3%NP-40/0.4 × SSC solution, 10 ~ 20s of vibration sloughs cover glass, soaks 5 ~ 10 minutes, by slide be placed in 37 DEG C go from
In sub- water, 1 ~ 3s is vibrated, is soaked 2 minutes, dark place spontaneously dries slide;
(13)Mounting:10uL DAPI counterstains are added dropwise;
(14)Diagosis:Under fluorescence microscope slide is observed from suitable optical filter;
(15)Result judgement:A. CD45 stained positives are leucocyte;B. CD45 is not colored, but is non-swollen in huge bare nucleus
Oncocyte;C. CD45 is not colored, signaling point >=2, and non-huge bare nucleus may determine that as circulating tumor cell.
10. application according to claim 9, it is characterised in that step(11)The condition of the hybridization incubation is:75 DEG C of changes
Property 2 minutes, 37 DEG C be incubated 2 hours.
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