CN1990498A - Method and apparatus for concentration and purification of nucleic acid - Google Patents
Method and apparatus for concentration and purification of nucleic acid Download PDFInfo
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- CN1990498A CN1990498A CN 200610141539 CN200610141539A CN1990498A CN 1990498 A CN1990498 A CN 1990498A CN 200610141539 CN200610141539 CN 200610141539 CN 200610141539 A CN200610141539 A CN 200610141539A CN 1990498 A CN1990498 A CN 1990498A
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Abstract
In a method for concentration and purification method of nucleic acids using electrophoresis, cationic surfactant is added to a sample containing nucleic acids so as to adjust electric charge of impurities in the sample, and then the sample is placed in an electric field for electrophoresis so as to concentrate and purify the nucleic acids. The cationic surfactant (4) adsorbs substance other than the nucleic acids so as to adjust the electric charge of the substance, and the adsorption of the cationic surfactant is adjusted by the added amount of nonionic surfactant. Alternatively, nucleic acids are contacted with a separation medium (108), and then recovered by a filter (104) whose cross sectional area is gradually decreased in the direction of migration.
Description
The application is the dividing an application of Chinese patent application 200380104540.4 of being entitled as of submitting on November 27th, 2003 method and apparatus of purification of nucleic acid " concentrate and ".
Technical field
The present invention relates to a kind of method of isolating nucleic acid.In more detail, the present invention relates to a kind of method of utilizing the electrophoretic separation target nucleic acid.
Background technology
Because to the deciphering of human genome, the difference relation between vital process and the gene is analyzed recently.Therefore, the medical science emphasis is transferred to nosetiology from pathology, transfers to prevention from therapeutic treatment.Therefore, technique of gene detection becomes important foundation.
Gene test can be used to the detection that is difficult to finish in the routine clinical inspection, for example, to cultivating the evaluation of difficult pathogenic micro-organism, when treating or at infection early detection pathogenic micro-organism with microbiotic, under the situation that suspection exists antibody to shift, detect antigen, investigation pathogenic micro-organism contagium, the individual discerns for example blood lineage's diagnosis, the gene diagnosis of the disease type of leukemia and solid tumor and the diagnosis of genetic diseases.Need the long-time bacterium of cultivating to be found by gene test effectively, because gene test spent time for the method for culturing bacterium is shorter.In addition, because DNA stable depends on good storage conditions, old sample, for example refrigerated living tissue test sample or bone also can be detected.
Gene test has attracted the public's attention, because it can expand the probability to the detection of the sexually transmitted disease (STD) of nearest increase.
As everyone knows, conventional nucleic acid purification and spissated method comprise and use phenol, chloroform or alcoholic acid purification process, use pillar or the purification process of strainer and the purification process of use magnetic silica pearl of absorption nucleic acid.
In addition, also has the well-known ordinary method that from the tabular gel electrophoresis, reclaims nucleic acid, as disclosing in Japanese Utility Model described in the flat 5-88296, its amplifying nucleic acid is electrophoresis on the gel of getting ready, one retrieving arrangement is moved to the gel section that contains target nucleic acid, and target nucleic acid is by further electrophoresis recovery then.
In addition, disclose well-known ordinary method such described in the flat 8-327595 just like Japan special permission, electrophoresis is with a minute isolated target nucleic acid in the tabular gel for its amplifying nucleic acid, and one section is reclaimed sheet (chip) and is inserted in the gel near the target nucleic acid band with the recovery target nucleic acid.
About the nucleic acid purification and the concentration method of routine, use phenol, chloroform or alcoholic acid purification process only can under limited environment, utilize, because this need require the active drug of senior chemical device.Further, be difficult to make this purification process automatization, because this needs the operation and the high speed centrifugation step of difficulty.Also be difficult to obtain high precision.
Application pillar or strainer adsorb the purification of nucleic acids method to be undertaken by fluent solution.Therefore, when a sample comprised many impurity such as rubbish, the often blocked purification efficiency that causes of pillar or strainer reduced.In addition, be difficult to make this method automatization, because it requires the step of centrifugal or sucking-off.
The recovery method of applied magnetic silica beads is difficult to obtain the height recovery of nucleic acid, because can not be reclaimed by magnet or may be retained in the sample from the silica beads that magneticsubstance falls.
Conventional reclaims the method requirement tabular running gel of nucleic acid and the gel section that comprises target nucleic acid is handled the electrophoresis of nucleic acid the tabular running gel before from the tabular running gel.
It is very weak to be used for the antishock ability of electrophoretic gel, and according to the change on its forming process possibility occurrence characteristics.Therefore, in general, the position of target nucleic acid in running gel analyzed by ultraviolet ray behind electrophoresis, and the gel section that contains the high density target nucleic acid subsequently is processed.
Therefore, each of gene test of using this method detects and all to need to spend long time.If it is very big to be used for electrophoretic gel,, therefore reduced the recovery of nucleic acid because the unbalanced nucleic acid belt trace that causes of gel increases.In addition, this big gel needs strong electric power to be used for electrophoresis.
Summary of the invention
As the various result of experiment that address the above problem, found a kind of following method, promptly in sample, add tensio-active agent and be present in impurity in the sample, thereby make the mobile of impurity be different from moving of nucleic acid, and impurity is opened from separate nucleic acid with absorption.
In addition, except epinucleic impurity through cats product and nonionic surface active agent and charged, and be placed in the electric field, its amplifying nucleic acid is separated from the sample that contains impurity and purifying is concentrated to be concentrated or to be easy to.
Fig. 1: under the condition that tensio-active agent exists, utilize the mimic diagram of electrophoresis condensed nucleic acid.Sample contains nucleic acid 1 and impurity 2.Tensio-active agent is added in the sample.Nonionic surface active agent 3 and cats product 4 are used as tensio-active agent.SURFACTANT ADSORPTION impurity 2 with sample mix.Impurity 2 positively chargeds that adsorbed by cats product 4, thus with seldom or not separated by the nucleic acid 1 of SURFACTANT ADSORPTION.Correspondingly, impurity 2 can easily be removed from sample with condensed nucleic acid 1.
Below, will explain the method for a condensed nucleic acid.In the method, carry out twice electrophoresis to guarantee concentrating to nucleic acid.Ion excessive in the sample was removed in the electrophoresis in the first time, and the nucleic acid in the sample was concentrated in the electrophoresis in the second time.At first, the 1%Triton of 100 μ L (registered trademark) X-100 is with being that nonionogenic tenside is added in the sample that contains nucleic acid and mixing, then 96 ℃ of heating 10 minutes.Then, the 0.2%DPC of 100 μ L is used as cats product and is added in the sample.Perhaps, nonionogenic tenside and cats product can add before heat treated simultaneously.Even nucleic acid is present in the prokaryotic cell prokaryocyte of colibacillus or similar bacterium, cell walls is added to and is used for pretreated tensio-active agent in the sample and destroys.Correspondingly, the nutrient solution of colibacillus or similar bacterium can be used as sample, thereby helps the operation to sample pretreatment.Carry out pre-treatment as described above, the volts DS that applies 100V carried out electrophoresis 10 minutes, thereby removed excessive ion from sample.Subsequently, thus the volts DS that applies 125V-150V carries out electrophoresis was recovered to nucleic acid at positive pole in 120 minutes.
Below explanation is used for the structure of the electrophoresis chamber of sample electrophoresis.For the electrophoresis first time, Fig. 2 represents to be used for the structure of electrophoretic electrophoresis chamber 5 for the first time.Sample groove 6 is arranged in the electrophoresis chamber 5 and electrophoresis chamber 5 is divided into side of the positive electrode part and negative side next door 9 partly.Sample cell 6 runs through next door 9, and the anodal protrusion of one side direction, and a side direction negative pole protrudes.Sample cell 6 both ends opens, and opening portion seals with gel 8.In sample cell 6, produced potential difference to carry out electrophoresis to nucleic acid with by the impurity of SURFACTANT ADSORPTION.Nonionogenic tenside and cats product both are added in the sample, and heated sample.Then, sample is injected in the sample cell 6.Between electrode, use the voltage of 100V to carry out electrophoresis 10 minutes.Correspondingly, excessive ion is removed from sample.After removing excessive ion, nucleic acid concentrates by electrophoresis for the second time.
Electrophoresis explanation for the second time: the sample cell 6 that contains the sample that is injected in the electrophoresis process in the first time is connected to an accumulator tank and is placed on and carries out the electrophoresis second time in the electrophoresis chamber.Fig. 3 represents to be used for the structure of electrophoretic electrophoresis chamber 5 for the second time.Sample cell 6 is arranged, accumulator tank 7 and electrophoresis chamber 5 divided into side of the positive electrode part and negative side next door 9 partly in the electrophoresis chamber 5.Sample cell 6 runs through next door 9, and protrudes to negative side.Accumulator tank 7 inserts next door 9 and protrudes to side of the positive electrode.Pass gel 8 and be connected with each other at sample cell 6 and accumulator tank 7 next doors 9 places.Sample cell 6 both ends opens, and opening portion is respectively by gel 8 sealings.Accumulator tank 7 both ends opens.An end that is positioned at the accumulator tank 7 of negative side is sealed by gel 8, and an end that is positioned at the accumulator tank 7 of side of the positive electrode seals with ultra-filtration membrane 11.As the above-mentioned electrophoresis chamber that constitutes, pass electrode with the voltage of 120V and carried out electrophoresis 120 minutes.
By the electrophoresis second time that in electrophoresis chamber, carries out, remove the part of sample except that nucleic acid after the excess amount of ions by electrophoresis, its amplifying nucleic acid can be recovered in the accumulator tank 7 effectively.The ultra-filtration membrane that side of the positive electrode provided 11 at accumulator tank 7 stops nucleic acid to spill from accumulator tank 7.Correspondingly, the organic efficiency of nucleic acid can improve.If the state of sample is suitable, can only carry out electrophoresis and do not carry out the electrophoresis first time second time.Pretreated sample is injected in the sample cell 6 that is connected on the accumulator tank 7 and carries out electrophoresis, and its amplifying nucleic acid can be concentrated at an easy rate.The excess amount of ions that is present in the sample can be passed through ultra-filtration membrane, thereby does not influence the recovery of nucleic acid.
That is to say,, a kind ofly utilize electrophoresis to concentrate and the method for purification of nucleic acid is characterised in that sample is placed in the electric field to concentrate and purification of nucleic acid after having regulated the carrying capacity that is present in the impurity in the sample that contains nucleic acid according to the present invention.Further, according to the present invention, a kind ofly utilize the electrophoresis to concentrate and the method for purification of nucleic acid is characterised in that has added the carrying capacity that cats product is regulated the impurity in the sample in containing the sample of nucleic acid, this sample is placed in the electric field in order to concentrating and purification of nucleic acid with electrophoresis then.Cats product and nonionogenic tenside are added to the carrying capacity that is present in the impurity in the sample in the sample that contains nucleic acid with adjusting, and then, this sample is placed in the electric field in order to concentrating and purification of nucleic acid with electrophoresis.The electric charge that removes epinucleic other material in the sample is adsorbed onto on the cats product by it to be regulated, and these materials are regulated by the amount of regulating the nonionogenic tenside that adds the absorption of cats product.
According to the present invention, be used for concentrating and the device of purification of nucleic acid contains cats product and the nonionogenic tenside that adds sample to, sample wherein by electrophoresis to concentrate and purification of nucleic acid at side of the positive electrode.Further, this device contains a container, and its sidewall is formed by isolator.In container, contain one and be used to stop the conduction chorista of diffusion, thereby internal tank is divided into sample flood chamber and nucleic acid recovery chamber.Every end of this container is connected respectively on the electrode by dashpot.
Perhaps, also can use following method.The sample that contains nucleic acid contacts with the separating medium that is formed by a kind of material, and in this material, the material with different molecular weight shows different mobilities, adds that voltage is with nucleic acid and other separating substances.Then, the nucleic acid by separating medium is reclaimed by a strainer.This strainer has the aperture by nucleic acid, and this aperture is littler than target nucleic acid.
For example, an end that is used for electrophoretic separating medium is furnished with the sample supply part of filling with damping fluid, is furnished with the sampling part of filling with damping fluid at the other end.By sample supply part and sampling part are applied voltage, sample is electrophoretic migration in separating medium.Since the different molecular weight of each nucleic acid, the nucleic acid in the sample in separating medium with different speed migrations, thereby cause having the different time of the nucleic acid needs of different molecular weight by separating medium and be eluted in the sampling part.Consider such situation, after target nucleic acid is eluted to the sampling part end, stop electrophoresis at once, to reduce target nucleic acid component in addition.The damping fluid of sampling part can be changed according to keep forging ahead time of sample part of target nucleic acid wash-out, with from sampling part sampling target nucleic acid only.The concentration of target nucleic acid depends on the amount of the damping fluid in the sampling part.
Like this, aforesaid operations is automated operation easily, because it does not require centrifugal or suction operation.Nucleic acid can be separated from sample at once in a large number.Contain the elute soln of target nucleic acid by minimizing, solution is concentrated to increase the concentration of target nucleic acid in sample.Further, be purified with the such nucleic acid that is easy to process and behind electrophoresis, taken a sample immediately, thereby carry out the transition to next step reposefully by current step.
Be compared to other method, the inventive method can obtain the higher rate of recovery and more high-precision target, and does not need expensive reagent or expensive device, thereby has reduced running cost and running cost.In this, utilize electrophoresis to concentrate and the method for purification of nucleic acid according to of the present invention, containing the impurity that exists in the sample of nucleic acid contacts with a kind of separating medium, in this medium, have being moved with different mobilities according to the difference of molecular weight of different molecular weight by electrophoretic nucleic acid, then, nucleic acid less than target nucleic acid passes the strainer with the sectional area that reduces on migratory direction, and target nucleic acid is reclaimed by strainer, thereby isolates target nucleic acid from sample.This method can be carried out under the situation of not carrying out centrifugal and suction operation, and can use a simple device to separate and condensed nucleic acid.Further, such simple structure can realize automatization at an easy rate.Further, can obtain a large amount of samples at once.Can reduce the elute soln that contains target nucleic acid to concentrate and to increase the concentration of target nucleic acid in the sample.Separation and spissated running cost and operating time all have been lowered.In addition, be used to identify that the detection of initial non-existent foreign gene can carry out at an easy rate.
Description of drawings:
Fig. 1 is under the condition that tensio-active agent exists, and utilizes the mode chart of electrophoresis condensed nucleic acid.
Fig. 2 is used for the diagram of electrophoretic electrophoresis chamber for the first time.
Fig. 3 is used for the diagram of electrophoretic electrophoresis chamber for the second time.
Fig. 4 is the diagram of first electrophoresis chamber.
Fig. 5 is the diagram of second electrophoresis chamber.
Fig. 6 is the skeleton view of sampling unit.
Fig. 7 is the orthographic plan of sampling unit.
Fig. 8 is the side elevational view of sampling unit.
Fig. 9 is the side cross-sectional views of sampling unit.
Figure 10 is the skeleton view of connection section.
Figure 11 is the side cross-sectional views of connection section.
Figure 12 is the side cross-sectional views of filter house.
Figure 13 is the assembling side elevational view of separating unit.
Figure 14 diagrammatic is the ultraviolet spectrogram that is recovered solution.
Figure 15 is a nucleic acid upgrading unit part profile perspective.
Figure 16 is the orthographic plan of nucleic acid upgrading unit.
Figure 17 is the side elevational view of nucleic acid upgrading unit.
Figure 18 diagrammatic is the concentration process of target nucleic acid.
Figure 19 is the diagram of the Kaifeng process of upgrading unit.
Figure 20 is the side cross-sectional views of upgrading unit.
Preferred forms of the present invention:
Below provide explanation to embodiments of the present invention.At first, use description to electrophoretic electrophoresis chamber.Fig. 4 diagrammatic is one first electrophoresis chamber 21.Electrophoresis chamber 21 is divided into negative electrode side channel 22 and anodal side channel 23 by next door 24 and 25. Next door 24 and 25 is positioned at the central authorities of electrophoresis chamber 21, and sampling unit 26 is attached on next door 24 and 25.One end of sampling unit 26 protrudes in the negative pole side channel, and the other end protrudes in the anodal side channel 23.The side of the positive electrode of sampling unit 26 and negative side be partially filled gel, and its side surface has a filling orifice, is injected in the sample unit by this hole sample.During electrophoresis, inject bore closure with a stopper.Negative pole is inserted in the negative pole side channel 22, and positive pole is inserted in the anodal side channel 23, so that electrophoresis chamber 21 is applied voltage.
Another electrophoresis chamber has below been described.Fig. 5 illustrates one second electrophoresis chamber 21.Second electrophoresis chamber 21 is divided into negative electrode side channel 22 and anodal side channel 23 by next door 24 and 25. Next door 24 and 25 is positioned at the central authorities of electrophoresis chamber 21, and separating unit 32 is attached on next door 24 and 25.One end of separation unit 32 protrudes in the negative pole side channel 22, and its other end protrudes in the anodal side channel 23.Negative pole is inserted in the negative pole side channel 22, and positive pole is inserted in the anodal side channel 23, so that electrophoresis chamber 21 is applied voltage.Separating unit comprises 3 unit, i.e. sampling unit 26, connection section 33 and filter house 34, and they interconnect.O type ring is between sampling unit 26 and the connection section 33 and between connection section 33 and the filter house 34, with the connection of guaranteeing them and prevent that damping fluid from flowing out.The negative pole one side part of sampling unit 26 is gel filled, and the positive pole one side part of connection section 33 is also gel filled.One ultra-filtration membrane is attached to filter house 34.
Nucleic acid is concentrated in such electrophoresis chamber.At first, for the electrophoresis first time, a kind of sample dissolution is injected into by filling orifice, then with this bore closure.Then, sampling unit 26 is positioned in and makes in the electrophoresis chamber 21 that the upper surface of sampling unit 26 protrudes from solution slightly.Subsequently, the volts DS that applies 100V carries out 20 minutes electrophoresis, thereby removes excessive ion from sample.Damping fluid is prepared by 1xTAE solution, 40mM Tris, 40mM Glacial acetic acid and 1mM EDTA, and its pH is adjusted to 8.0.
After removing excessive ion from first electrophoresis chamber 21, connection section 33 and filter house 34 are connected to sampling unit 26.O type ring is positioned at each junction and comes out to prevent solution stream.Be added in the connection section 33 with 6: 4 mixed 100% ethanol and 1xTAE prepared solution, TE-1 (pH 8.0 for 10mM Tris-HCl, 0.1mM EDTA) is added in the sampling unit 26.
Next the structure of sampling unit 26, connection section 33 and filter house 34 is described.The structure of sampling unit 26 is at first described.Fig. 6 is the skeleton view of sampling unit, and Fig. 7 is the orthographic plan of sampling unit, and Fig. 8 is the side elevational view of sampling unit, and Fig. 9 is the side cross-sectional views of sampling unit.Sampling unit comprises a container that is used to hold gel.This container is processed with Microcon (registered trademark) YM-3 centrifuge container unit (Millipore), and ultra-filtration membrane is removed from it like this, and has the hole of a 5mm diameter therein.Perhaps, any unit can be used as sampling unit 26, as long as it has identical functions.
Below will explain connection section 33.Figure 10 is the skeleton view of connection section, and Figure 11 is the side cross-sectional view of connection section.Similar to sampling unit 26, the processed ultrafilter membrane that makes in the centrifuging unit of Millipore is removed, and has the hole of 5mm diameter in the unit, thereby has constituted connection section 33.Connection section 33 comprises a right cylinder 41 and a pedestal 43.Right cylinder 41 is connected in pedestal 43.Pedestal 43 is made into the scalariform cylinder, and a vertical hole 44 penetrates pedestal 43.Gel 48 with thickness of several millimeters is placed in the right cylinder 41.In right cylinder 41, gel 48 is placed in the upper surface of pedestal 43 to prevent that liquid from flowing out or flow to filter house 34 from sampling unit 26.
Below explain filter house 34.Figure 12 is the side cross-sectional views of filter house.Filter house 34 also constitutes by the centrifuging unit of processing Millipore.Filter house 34 comprises a right cylinder 41 and a pedestal 43.Right cylinder 41 is connected on the pedestal 43.This right cylinder 41 is than the right cylinder of sampling unit 26 and right cylinder 41 short about 5mm of connection section 33.Pedestal 43 is made into the scalariform cylinder, and a upright opening 44 penetrates pedestal 43.In right cylinder 41, ultra-filtration membrane 49 is placed in the upper surface of pedestal 43 preventing that nucleic acid from flowing out, thereby guarantees concentrating of nucleic acid.
Next, explain the embodiment of nucleic acid concentration operation.Sample is the colibacillus nutrient solution, carry out the first time and for the second time electrophoresis with condensed nucleic acid.The concentration of the nucleic acid that reclaims is measured by the light absorption ratio method of masurement.The nutrient solution of the colibacillus of 100 μ L (Escherichia coli DH5 α) is used as sample.The 1%Triton of 100 μ L (registered trademark) X-100 is added in the sample, and heats 10 minutes under 96 ℃ of conditions.Subsequently, the 0.2%DPC of 100 μ L is added to wherein, thereby preparation is used for electrophoretic sample.0.5xTAE be used as electrophoretic buffer.Agarose is dissolved among the 1xTAE.In addition, this 1xTAE solution is from 40mM Tris, and 40mM Glacial acetic acid and 1mM EDTA prepare, and its pH is adjusted to 8.0.
Preparation is used for electrophoretic sample and joins sampling unit 26 by filling orifice 42, then with bore closure.Electrophoresis chamber is divided into negative side part and side of the positive electrode part by sealing (putty), and 0.5xTAE is added into the two side portions of groove.Sampling unit 26 be placed on sealing sentence make sampling unit 26 upper surface than damping fluid height.Subsequently, apply the volts DS of 100V and carry out the electrophoresis 20 minutes first time.
After electrophoresis was finished for the first time, connection section 33 and filter house 34 were connected on the sampling unit 26, with the structure separating unit, and carried out the electrophoresis second time.
Below will provide embodiment to electrophoretic operation for the second time.Be added in the connection section 33 with 6: 4 mixed, 100% ethanol and 1xTAE gained solution.(10mMTris-HCl, 0.1mM EDTA pH8.0) are added in the sampling unit 26 TE-1.
Next, connection section 33 and filter house 34 are connected on the sampling unit 26 with the assembling separating unit.Figure 13 is a separating unit assembly structure side elevational view.Separating unit is from assembling towards unidirectional sampling unit 26, connection section 33 and filter house 34.O type ring 51 is placed between connection section 33 and the filter house 34, and between connection section 33 and the filter house 34, flows out from separating unit to prevent solution.
Electrophoresis chamber is divided into negative side part and side of the positive electrode part by sealing, and 0.5xTAE is added into the both sides of groove.Put into the separating unit of assembling so that sampling unit 26 is placed in the negative side of sealing, filter house 34 is placed in the side of the positive electrode of sealing.Subsequently, apply the volts DS of 100V and carry out the electrophoresis 240 minutes second time.
Next, nucleic acid solution reclaims at filter house 34, and its light absorption ratio is measured the concentration that reclaims nucleic acid to calculate by ultraviolet spectrogram.Figure 14 diagrammatic is the ultraviolet spectrogram that reclaims solution.The nucleic acid concentration that calculates is 32.3ng/ μ L (6.7 * 10
6Individual copy/μ L).The concentration of nucleic acid is so calculated, and the light absorption ratio of locating at 260nm (A260) multiply by nucleic acid inherent coefficient, multiply by the path length (mm) of cuvette, again divided by 10.
The purity of the nucleic acid that reclaims is calculated by ultraviolet spectrogram.The purity of the recovery nucleic acid that calculates is 1.91.Purity is calculated divided by the light absorption ratio that 280nm (A280) locates with the light absorption ratio that 260nm (A260) locates.When sample is a purity when being 100% DNA, calculated value is about 1.8.When sample is a purity when being 100% RNA, calculated value is about 2.0.Being blended in the protein in the tested material and the amount of phenol reacts with the value of A280.When light absorption ratio is lower than 1.5, may sneak into lower-molecular substance, for example protein.
Utilize electrophoresis to concentrate and the method for purification of nucleic acid according to of the present invention, the carrying capacity that contains the impurity in the sample of nucleic acid is conditioned, and sample is placed in and carries out electrophoresis in the electric field to concentrate and purification of nucleic acid then.As a result of this method, the migration of nucleic acid is different from the migration of impurity during electrophoresis, can isolate nucleic acid effectively like this.Difference in migration between impurity and nucleic acid can be regulated by the adjusting of carrying capacity, thereby can control migration easily.Need not to use separating centrifuge or allied equipment, thereby the device that is used for condensed nucleic acid can be very compact.
According to utilizing electrophoresis to concentrate and the method for purification of nucleic acid, cats product is added in the sample that contains nucleic acid, be present in the carrying capacity of the impurity in the sample with adjusting, then, this sample is placed on and carries out electrophoresis in the electric field to concentrate and purification of nucleic acid.Owing to cats product, the operation of this method is easy to, and the security of operation can be guaranteed at an easy rate.By increasing the absorption to impurity, the difference in migration between impurity and nucleic acid becomes greatly to be separated to nucleic acid effectively.Impurity and nucleic acid are opposite direction migration in case impurity reduces the purity of nucleic acid, thus purification of nucleic acid easily.
Utilize electrophoresis to concentrate and the method for purification of nucleic acid according to of the present invention, cats product and nonionic surface active agent are added in the sample that contains nucleic acid, be present in the carrying capacity of the impurity in the sample with adjusting, this sample is placed on and carries out electrophoresis in the electric field to concentrate and purification of nucleic acid then.Correspondingly, the absorption of cats product can be undertaken by regulating cats product and nonionic surface active agent ratio between the two, thereby can easily regulate by the migration of electrophoretic impurity.Thereby nonionic surface active agent absorption nucleic acid prevents cats product absorption nucleic acid.
The carrying capacity of other material beyond the nucleic acid is adsorbed onto cats product by it and regulates, and this absorption is then regulated by the amount of the nonionic surface active agent that adds.Correspondingly, ratio and the nonionic surface active agent easily Be Controlled of impurity absorption to the cats product.In addition, the carrying capacity of impurity can be regulated by simple operation.Nonionic surface active agent is adsorbed onto on the nucleic acid to prevent cats product absorption nucleic acid.
In device, cats product and nonionic surface active agent are added in the sample, then this sample by electrophoresis to concentrate and purification of nucleic acid at side of the positive electrode.Correspondingly, this device can be simplified the nucleic acid in the purification of samples and regulate and control the migration of nucleic acid, thereby self is very compact when guaranteeing security.
Utilize electrophoresis device concentrated and purification of nucleic acid to comprise a container, the sidewall of this container is formed by isolator.This container is used to prevent that the electroconductibility separating medium that spreads is divided into the sample flood chamber and nucleic acid reclaims the chamber.The two ends of this container are connected respectively to two electrodes by buffering liquid groove.Therefore, thus be used for concentrating and the device of purifying can constitute easily and reduces its production cost.In addition, the security of height is controlled and had to this device easily.
Next, hereinafter with reference to accompanying drawing second embodiment of the present invention is described.
Figure 15 is a nucleic acid upgrading unit part profile perspective, and Figure 16 is this unitary orthographic plan, and Figure 17 is this unitary side elevational view.Nucleic acid upgrading unit shown in Figure 15-17 below will be described.
The upgrading unit 101 that is arranged in the t-DNA detector separates and enriched target nucleic acid.Upgrading unit 101 comprises flood chamber 102, the separate chamber 108 and the sampling hut 103 that are formed by separating medium.The sample that contains target nucleic acid is injected into flood chamber by geat 109, and flood chamber 102 and sampling hut 103 are applied voltage so that the nucleic acid migration enters in the sampling hut 103.The target nucleic acid by separate chamber 108 flow in the sampling hut 103, and takes a sample from sampling hut 103 by geat 110.Biological sample, for example blood, urine, sputum or analogue, beverage or food can be used as sample and be injected in the flood chamber 102.In addition, genome or plasmid also can be injected into.
The structure of each part in the upgrading unit 101 below will be described in detail in detail.Flood chamber 102 is connected to an end of separate chamber 108, and sampling hut 103 is connected to the other end of separate chamber 108.Electrode 105 is placed in the flood chamber, and electrode 106 and 107 is placed in the sampling hut 103.Flood chamber 102 and sampling hut 103 fill damping fluid and are used for electrophoresis.Electrode 106 in the sampling hut 103 is placed in the face of the electrode in the flood chamber 102, and the electrode 107 in the sampling hut 103 is placed in the bottom of sampling hut 103.Strainer 104 is placed in the sampling hut 103 sampling hut 103 is divided into separate chamber 108 and the chamber that comprises electrode 106.Strainer 104 allows to pass through less than the material of target nucleic acid, stops the material that is not less than target nucleic acid to pass through.A lot of filter openings are arranged on the strainer 104, and they have for example prevention and target nucleic acid interacts and stop target nucleic acid by such characteristic.
Next, will explain by the concentration process of upgrading unit according to Figure 18 target nucleic acid.Figure 18 is the synoptic diagram of the concentration process of target nucleic acid.At first, Figure 18 (a) expression sample is injected into the state in the flood chamber 102.For more clearly describing at this, our assumes samples contains target nucleic acid 112, greater than the nucleic acid 111 of target nucleic acid 112 (volume is big or big on the molecular weight amount), less than the nucleic acid 113 of target nucleic acid.
The state that Figure 18 (a) expression large nucleic acids 111, target nucleic acid 112 and small nucleic acids 113 are mixed.When voltage is applied on electrode 105 and 106, large nucleic acids 111, target nucleic acid 112 and small nucleic acids 113 are introduced in the separate chamber 108, and move with different speed in separate chamber 108, shown in Figure 18 (b).For structure shown in Figure 180, sepharose is used as separating medium and is filled separate chamber 108, so that small nucleic acids 113 is positioned at before other nucleic acid.
Small nucleic acids 113 arrives sampling hut 103 by separate chamber 108 the preceding.Then, small nucleic acids 113 passes strainer 104 and moves to electrode 106 in the sampling hut 103.Subsequently, target nucleic acid 112 arrives sampling hut 103 by separate chamber 108.Therefore, shown in Figure 18 (c), strainer 104 stops target nucleic acid 112 further to electrode 106 migrations.Because strainer 104 is made to taper, its bottom opening is towards the separate chamber 108, its lateral opening upwards, target nucleic acid 112 is concentrated in the part of strainer 104 facing to electrode 106.
In this state, stop to apply voltage by electrode 105 and 106, voltage applies by electrode 107 and 106, shown in Figure 18 (d).As a result, the electrode 106 little impurity of capture ratio target nucleic acid still.When the voltage that applies by two electrodes was stopped, nucleic acid was released from strainer.Like this, the process of target nucleic acid 112 under strainer discharges, prevented the diffusion of little impurity and small nucleic acids 113, thus high precision enriched target nucleic acid 112.
Then, the time of target nucleic acid 112 by separate chamber 108 calculated with determine from sample be injected into flood chamber 102, from by electrode 105 and 106 setting-up times to the change of the voltage by electrode 107 and 106, thereby automatically carry out the separation of target nucleic acid and concentrate.
Anyly be used for electrophoretic gel, for example sepharose can be used as separate chamber 108.Also can use separating medium as column filling.For example, be used for the carrier of gel-filtration, as using Sephadex (registered trademark) (Pharmacia).Also considerable is to be used for electrophoretic gel and column filling is combined and it is regulated so that target nucleic acid flows out at first in separated part 108.
Below, will another structure according to the upgrading unit of Figure 19 and Figure 20 be made an explanation.Figure 19 is the synoptic diagram of the Kaifeng process of upgrading unit, and Figure 20 is the side cross-sectional views of upgrading unit.Upgrading unit is inserted in the proofing unit to separate and enriched target nucleic acid.
The upper surface of upgrading unit 116 is pasting film 117a and 117b, and electrode 105 and 106 exposes in the side of upgrading unit 116.Electrode 107 exposes in its bottom surface.Electrode 105 is connected to flood chamber, and electrode 106 and 107 is connected to the sampling hut.Separate chamber 108 is arranged in the upgrading unit 116, and flood chamber and sampling hut are filled with electrophoretic buffer.The sampling hut is filtered device separately.
In this state, the sealed and voltage of upgrading unit 116 can be applied thereto from the outside.Correspondingly, upgrading unit can be easy to operate.When sample is injected in the upgrading unit 116 so that target nucleic acid is taken a sample, film 117a and 117b are torn as shown in figure 19, and sample is injected into so that target nucleic acid is taken a sample.Because film 117a and 117b are secured on the upper surface of upgrading unit, when tearing film 117, separate chamber 108 are not applied any big impact, thereby can stably concentrate and separate.
Industrial applicibility:
As above-mentioned, method of the present invention has been simplified nucleic acid has been concentrated and the operation of purifying, and According to of the present invention structurally very simple for concentrating with the device of purifying of nucleic acid, therefore can Be used for automatic detection device to concentrate and to detect nucleic acid.
Claims (1)
1. one kind is carried out electrophoresis with device concentrated and purification of nucleic acid, a container that it is characterized in that having the sidewall that is formed by isolator is prevented that by one the conduction separating medium that spreads is divided into the sample flood chamber and nucleic acid reclaims the chamber, and the buffering liquid groove of the two ends of this container by separately is connected respectively on two electrodes.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2002345210 | 2002-11-28 | ||
| JP2002345210 | 2002-11-28 | ||
| JP2003379796 | 2003-11-10 |
Related Parent Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2003801045404A Division CN1332972C (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN1990498A true CN1990498A (en) | 2007-07-04 |
Family
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Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2003801045404A Expired - Fee Related CN1332972C (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
| CN 200610141539 Pending CN1990498A (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
| CNB200610141538XA Expired - Fee Related CN100491391C (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2003801045404A Expired - Fee Related CN1332972C (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB200610141538XA Expired - Fee Related CN100491391C (en) | 2002-11-28 | 2003-11-27 | Method and apparatus for concentration and purification of nucleic acid |
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| CN (3) | CN1332972C (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106770596A (en) * | 2016-12-02 | 2017-05-31 | 中国科学院生态环境研究中心 | Washing device for Protein Separation and use its column gel electrophoresis apparatus |
| CN110656108A (en) * | 2019-10-31 | 2020-01-07 | 东莞市东阳光诊断产品有限公司 | Chip, nucleic acid extraction and purification device, and nucleic acid extraction and purification method |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101619289B (en) * | 2008-06-30 | 2012-04-25 | 广东出入境检验检疫局检验检疫技术中心 | Device for enriching and purifying long-fragment nucleic acid |
| CN102824854A (en) * | 2011-06-15 | 2012-12-19 | 杜权 | Electrophoresis apparatus and its application |
| WO2012171329A1 (en) * | 2011-06-15 | 2012-12-20 | Du Quan | Method for separating nucleic acid and use thereof |
| EP2886184A1 (en) * | 2013-12-23 | 2015-06-24 | Medizinische Universität Innsbruck | Electrochemical cell |
| CN107058075B (en) * | 2017-06-20 | 2023-10-20 | 商丘师范学院 | Plant cell protoplast purification instrument and purification method |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH0599899A (en) * | 1991-09-18 | 1993-04-23 | Hitachi Ltd | Method for separately purifying bio-substance |
| US6129828A (en) * | 1996-09-06 | 2000-10-10 | Nanogen, Inc. | Apparatus and methods for active biological sample preparation |
| US6146511A (en) * | 1998-01-30 | 2000-11-14 | The Perkin-Elmer Corporation | Electrophoretic nucleic acid purification method |
| US6699986B2 (en) * | 1998-08-04 | 2004-03-02 | Ortho-Clinical Diagnostics, Inc. | Electrophoretic separation of nucleic acids from proteins at low ph |
| EP1180238A1 (en) * | 1999-05-19 | 2002-02-20 | Bilatec AG | Device and method for isolating electrically charged molecules |
| US7001724B1 (en) * | 2000-11-28 | 2006-02-21 | Applera Corporation | Compositions, methods, and kits for isolating nucleic acids using surfactants and proteases |
-
2003
- 2003-11-27 CN CNB2003801045404A patent/CN1332972C/en not_active Expired - Fee Related
- 2003-11-27 CN CN 200610141539 patent/CN1990498A/en active Pending
- 2003-11-27 CN CNB200610141538XA patent/CN100491391C/en not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN106770596A (en) * | 2016-12-02 | 2017-05-31 | 中国科学院生态环境研究中心 | Washing device for Protein Separation and use its column gel electrophoresis apparatus |
| CN106770596B (en) * | 2016-12-02 | 2019-03-01 | 中国科学院生态环境研究中心 | Washing device for Protein Separation and the column gel electrophoresis apparatus using it |
| CN110656108A (en) * | 2019-10-31 | 2020-01-07 | 东莞市东阳光诊断产品有限公司 | Chip, nucleic acid extraction and purification device, and nucleic acid extraction and purification method |
| CN110656108B (en) * | 2019-10-31 | 2021-06-08 | 东莞市东阳光诊断产品有限公司 | Chip, nucleic acid extraction and purification device, and nucleic acid extraction and purification method |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1717412A (en) | 2006-01-04 |
| CN100491391C (en) | 2009-05-27 |
| CN1990497A (en) | 2007-07-04 |
| CN1332972C (en) | 2007-08-22 |
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