CN106290924A - A kind of immunochromatographiassays assays test kit - Google Patents
A kind of immunochromatographiassays assays test kit Download PDFInfo
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- CN106290924A CN106290924A CN201610612136.7A CN201610612136A CN106290924A CN 106290924 A CN106290924 A CN 106290924A CN 201610612136 A CN201610612136 A CN 201610612136A CN 106290924 A CN106290924 A CN 106290924A
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- Prior art keywords
- antibody
- detectable substance
- concentration
- outer shroud
- film
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/92—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving lipids, e.g. cholesterol, lipoproteins, or their receptors
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/558—Immunoassay; Biospecific binding assay; Materials therefor using diffusion or migration of antigen or antibody
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/577—Immunoassay; Biospecific binding assay; Materials therefor involving monoclonal antibodies binding reaction mechanisms characterised by the use of monoclonal antibodies; monoclonal antibodies per se are classified with their corresponding antigens
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6854—Immunoglobulins
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/72—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving blood pigments, e.g. haemoglobin, bilirubin or other porphyrins; involving occult blood
- G01N33/721—Haemoglobin
Abstract
A kind of immunochromatographiassays assays test kit, including: it is arranged at the adhesive pad of bottom；The antibody being bonded on adhesive pad fixes film；Bed course, it is arranged at antibody and fixes the side of film, containing the antibody through label labelling；Adsorptive pads, it is arranged at antibody and fixes film opposite side；Sample pad, it is arranged at bed course side, fixes film connection side with bed course and antibody relative；Described antibody is fixed film and is arranged antibody dispensing area, and it includes internal ring and outer shroud；The anti-first detectable substance antibody of described internal ring coating；Described outer shroud is radially divided into the region that multiple area is identical；Described outer shroud regional is coated with the anti-second detectable substance antibody of variable concentrations successively；Described outer shroud regional marker readout respectively, this reading represents that the first detectable substance is relative to the first detectable substance and the concentration of the second detectable substance total amount.
Description
Technical field
The present invention relates to medical treatment detection analysis field, especially relate to a kind of immunochromatographiassays assays test kit and immunity layer
Analysis analytical reagent box preparation method.
Background technology
Immunoassay technology is using antibody or antigen as analytical reagent, and determinand carries out the inspection of qualitative or quantitative analysis
Survey method, its ultimate principle is exactly the interaction between antibody and antigen.Immunoassay technology has high specificity, sensitivity
The advantage such as high, easy, is the important research means of modern life science, before bioanalysis detection field has a wide range of applications
Scape.
It is new that immunochromatography technique is built upon on the basis of chromatographic technique and antigen one antibody specificity immunoreation
Emerging immunoassay technology.Immunochromatography technique is with fibre strip chromatographic material as solid phase, makes sample molten by capillarity
Liquid moves on chromatography strip, makes in sample the receptor (such as antigen or antibody) for determinand on determinand and chromatographic material simultaneously
There is specificity, the immunoreation of high-affinity.
In chromatography process, immune complex is enriched with or is trapped in the detection line of chromatographic material, and free revealing label
The receptor of substance markers then crosses detection band, is automatically separated with immune complex, and is enriched with in follow-up chromatography process or cuts
Stay another region (quality control band) of chromatographic material. by range estimation detection band and the color of quality control band, thus realize examining qualitatively
Survey the purpose of determinand.
Immunochromatographyassay assay technology because of have directly perceived, quick, detection efficiency is high, method is easy, pollution-free, expense is low
The advantages such as honest and clean, highly sensitive, high specificity, and it is widely used in clinical diagnosis, field condition and familial self detection, for
Redemption life is significant.
In prior art, Tianzhonggui Metal Industrial Co., Ltd is in the patent of invention of 201510017675.1, it is proposed that
The immunochromatographiassays assays test kit of a kind of two kinds of detected component ratio that can measure in Clinical detection sample, such as, be used for examining
Survey the immunochromatographiassays assays test kit of HbA1c Yu HbA0 ratio in blood sample, by HbA1c Yu HbA0 ratio-dependent inspection knot
Whether fruit belongs to negative or positive.But, the immunochromatographiassays assays test kit of this invention needs arrange color development signal and confirms
Device, when determining testing result, needs the result of HbA1c and HbA0 to confirm that device compares with color development signal respectively,
Feminine gender or the positive can be determined whether；And also cannot obtain quantitative result.
The present invention proposes the immunochromatographiassays assays test kit of a kind of improvement, it is possible to solve 201510017675.1 inventions special
The problems referred to above in profit, are quoted in full in the present invention.
Summary of the invention
As one aspect of the present invention, it is provided that a kind of immunochromatographiassays assays test kit, including: adhesive pad, it is arranged
In bottom, for bonding with the layer being arranged on；Antibody fixes film, and it is bonded on adhesive pad, and it arranges antibody coating
Region；Bed course, it is arranged at antibody and fixes the side of film, containing the antibody through label labelling；Adsorptive pads, it is arranged at anti-
Body fixes film opposite side, is used for absorbing unnecessary sample；Sample pad, it is arranged at bed course side, fixes film even with bed course and antibody
Connect side relative, be used for receiving sample；It is characterized in that: described antibody dispensing area is annular region, including internal ring and outer shroud；
The region that blocks water is set between described internal ring and outer shroud；The anti-first detectable substance antibody of described internal ring coating；The radially segmentation of described outer shroud
For the region that multiple areas are identical, the region that blocks water is set between regional；Described outer shroud regional is coated with different dense successively
The anti-second detectable substance antibody of degree；Described outer shroud regional respectively marker readout, this reading represent the first detectable substance relative to
First detectable substance and the concentration of the second detectable substance total amount.
Preferably, described immunochromatographiassays assays test kit is not provided with colorimetric card；Sample is at internal ring dispensing area and outer shroud
After dispensing area reacts, from outer shroud dispensing area, select the district consistent with the color development signal intensity of internal ring dispensing area
According to the reading in this region, territory, determines that the first detectable substance is relative to the first detectable substance and the concentration of the second detectable substance total amount.
Preferably, the concentration of each subregional anti-second detectable substance antibody of the dispensing area of described outer shroud is set, makes
First detectable substance corresponding to the concentration of the subregional anti-second detectable substance antibody of only one of which relative to the first detectable substance and
The concentration of the second detectable substance total amount is negative.
Preferably, being respectively provided with many sub regions outside each subregion of described outer shroud dispensing area, each sub regions depends on
The anti-second detectable substance antibody of secondary coating variable concentrations, the anti-second detectable substance antibody concentration of subregion coating is positioned at belonging to it divides
Regional concentration and higher than next subregion concentration subregional belonging to it between.
Preferably, the region that blocks water is set between described each sub regions.
Preferably, expression the first detectable substance that described each sub regions respectively labelling is corresponding is relative to the first detectable substance and the
The reading of the concentration of two detectable substance total amounts.
Preferably, the aperture at a circle interval is set at described internal ring by perforating device, is formed and tear tearing out of outlet encirclement
Region.
Preferably, described in tear out area bonded and tear shaping, this can be torn out region tear from internal ring by described shaping of tearing
Go out, for the coloring intensity of internal ring is compared with the coloring intensity of immediate subregional subregion.
Preferably, described first detectable substance is HbA1c, and described second detectable substance is HbA0.
As another aspect of the present invention, it is provided that the preparation method of a kind of immunochromatographiassays assays test kit, including such as
Lower step: (1) arranges the adhesive pad of bottom；(2) antibody is fixed film to be bonded on adhesive pad；(3) fix on film at antibody
The anti-first detectable substance antibody of endocyclic area coating；(4) anti-the of outer shroud subregion coating variable concentrations on film is fixed at antibody
Two detectable substance antibody；(5) by predetermined first detectable substance identical with the second detectable substance coloring intensity time, the second detectable substance is anti-
Bulk concentration and the first detectable substance, relative to the first detectable substance and the relation of the concentration of the second detectable substance total amount, are marked in outer shroud subregion
Remember that the first detectable substance is relative to the first detectable substance and the concentration value of the second detectable substance total amount；(6) at described outer shroud dispensing area
Being respectively provided with many sub regions outside each subregion, each sub regions is coated with the anti-second detectable substance antibody of variable concentrations successively,
The anti-second detectable substance antibody concentration of subregion coating be positioned at subregion concentration belonging to it with belonging to it subregional next
Between the concentration of subregion；(7) fix anti-igg linear with the position coating of annular region distance specific range on film at antibody to resist
Body；(8) fixing the side of film at antibody and arrange bed course, it contains the antibody through label labelling；(9) film is fixed at antibody
Opposite side arranges adsorptive pads；(10) side at bed course arranges sample pad.
Preferably, also include: (11) arrange the aperture at a circle interval by perforating device at internal ring, are formed and tear outlet encirclement
Tear out region；(12) tear shaping in described area bonded of tearing out, this can be torn out region from internal ring by described shaping of tearing
Tear out.
Accompanying drawing explanation
Fig. 1 is the top view of the immunochromatographiassays assays test kit of the embodiment of the present invention.
Fig. 2 is the side view of the immunochromatographiassays assays test kit of the embodiment of the present invention.
Fig. 3 is the dispensing area signal that the antibody of the immunochromatographiassays assays test kit that the present invention improves embodiment fixes film
Figure.
Detailed description of the invention
Embodiments of the invention are described below in detail, and the example of described embodiment is shown in the drawings, the most from start to finish
Same or similar label represents same or similar element or has the element of same or like function.Below with reference to attached
The embodiment that figure describes is exemplary, is only used for explaining the present invention, and is not considered as limiting the invention.And, should
Work as understanding, the feature not mutual exclusion of various embodiments described here, and can be in various combinations and transformation mistake
Journey exists.
Below as a example by detection blood sample HbA1c is relative to the ratio of HbA0, embodiments of the invention are described, wherein
HbA1c is the first detectable substance, and HbA0 is the second detectable substance.Should be appreciated that technical scheme is above-mentioned except can be used in
Outside detected material, it is also possible to by PSA (Free-PSA/Total-PSA ratio), (LDL gallbladder is solid for atherogenic index i.e. cholesterol
Alcohol/HDL cholesterol than) or the mark (albumins/globulins than) etc. of hepatic insufficiency or the nephrotic syndrome as tested
Survey material is analyzed.
See Fig. 1 and Fig. 2, the immunochromatographiassays assays test kit of the embodiment of the present invention, including: adhesive pad 1, antibody fixes film
2, bed course 3, adsorptive pads 4 and sample pad 5.Wherein, adhesive pad 1 is arranged at bottom, and its surface is adhesive surface, it is possible to will be arranged at
Layer thereon bonds.Antibody is fixed film 2 and is bonded on adhesive pad 1, and it arranges antibody dispensing area, and antibody is fixed film 2 and can be made
With fixing membrane material well known in the prior art, such as nitrocellulose filter (NC film) etc..
Antibody is fixed and is arranged antibody dispensing area on film 2, and antibody dispensing area includes annular region 21 and linear areas
22.Wherein annular region 21 is detection zone, and it is coated with anti-detectable substance antibody, it is possible to use known in the art prepares anti-detection
The scheme of thing antibody, such as the scheme in 201510017675.1 prepares anti-HbA1c antibody and anti-HbA0 antibody.Linear areas
22 is control line, and it is coated with linear anti-igg antibody,
Annular region 21 includes internal ring 211 and outer shroud 212, arranges the region that blocks water between internal ring 211 and outer shroud 212.Internal ring 211
The anti-first detectable substance antibody of coating.Outer shroud 212 is radially divided into the subregion that multiple area is identical, arranges resistance between regional
Aqua region.Each subregion of outer shroud 212 is coated with the anti-second detectable substance antibody of variable concentrations successively.Outer shroud 212 regional divides
Other marker readout, this reading represents that the first detectable substance is relative to the first detectable substance and the concentration of the second detectable substance total amount.This reading
Can predefine, by resisting the second detectable substance antibody for concentration known, change the first detectable substance phase in modeling sample
For the first detectable substance and the concentration of the second detectable substance total amount, until the first detectable substance reached and the luminescence of the second detectable substance
Colourity is identical, and now in this modeling sample, the first detectable substance in modeling sample is total relative to the first detectable substance and the second detectable substance
The reading that the anti-second detectable substance antibody of concentration extremely this concentration known of amount is corresponding.
Such as outer shroud 212 can be divided into three regions, regional be respectively coated 0.05mg/ml, 0.1mg/ml and
The anti-HbA0 Antibodies Monoclonal antibodies of 0.3mg/ml, the reading of its correspondence is 5.5%, 6.0% and 7.0%.Sample is at internal ring 211
After dispensing area and outer shroud 212 dispensing area react, select and internal ring 211 applying area from outer shroud 212 dispensing area
The region that the color development signal intensity in territory is consistent, gets final product the first detectable substance relative to the first detectable substance and according to the reading in this region
The concentration of two detectable substance total amounts.Such as, internal ring 211 and outer shroud 212 are labeled as 5.5% field color the most close, i.e. representing should
In sample, the first detectable substance is 5.5% relative to the concentration of the first detectable substance and the second detectable substance total amount.
Bed course 3 is arranged at antibody and fixes the side of film 2, containing the anti-hemoglobin antibodies through label labelling, permissible
As the scheme in 201510017675.1 prepares label solution, wherein make anti-hemoglobin Dan Ke of labelling in label solution
The amount of the gold contained in the liquid used by grand antibody-1 and anti-hemoglobin monoclonal antibody-2 is 10:1.Adsorptive pads 4, it sets
It is placed in antibody and fixes the opposite side of film 2, be used for absorbing unnecessary sample.Sample pad 5, it is arranged at bed course 3 side, with bed course 3 and
Antibody is fixed film 2 and is connected side relatively, is used for receiving sample, it is possible to use such as cellulosic filter paper, glass fiber filter paper is as sample
Product cushion material.
By the setting of the above-mentioned annular detection zone of the present invention, thus by the first detectable substance and the color development of the second detectable substance
Degree directly contrasts, and just can directly determine from the reading of outer region that the first detectable substance is relative to the according to the result of contrast
One detectable substance and the concentration of the second detectable substance total amount.Therefore have the advantage that 1, need not use color development signal to confirm device,
Can directly compare；2, quantitative determination reading can be carried out；3, internal ring the most directly closes on outer shroud regional, permissible
Internal ring is directly contrasted with outer shroud regional simultaneously.
The preferred embodiment of the invention, sees Fig. 3, is respectively provided with multiple outside each subregion of outer shroud 212 dispensing area
Subregion, each sub regions is coated with the anti-second detectable substance antibody of variable concentrations successively, anti-second detectable substance of subregion coating
Antibody concentration belonging to it subregion concentration and higher than next subregion concentration subregional belonging to it between.Each sub regions
Expression the first detectable substance that labelling is corresponding respectively is relative to the first detectable substance and the reading of the concentration of the second detectable substance total amount.Pass through
Above-mentioned setting, it is possible to more accurately determine dense relative to the first detectable substance and the second detectable substance total amount of the first detectable substance further
Degree.Preferably due to when checking that result is negative, user only needs result normally；And check when result is the positive, user
More concerned with definite detected value.Each subregional anti-second detectable substance that therefore, it can arrange the dispensing area of outer shroud 212 resists
The concentration of body so that it is in only have the first detectable substance corresponding to the concentration of a subregional anti-second detectable substance antibody relative to the
The concentration of one detectable substance and the second detectable substance total amount is negative.
Preferably, the aperture at a circle interval can be set at internal ring 211 by perforating device, formed and tear tearing of outlet encirclement
Go out region.Tear out area bonded tear shaping at this, tear shaping by this and this can be torn out region and tear out from internal ring 211, should
Tear in shaping is positioned over the subregional subregion of outer shroud 212 comparison comparing coloring intensity such that it is able to more accurate
Determine testing result.
Another embodiment of the presently claimed invention, it is provided that the preparation method of above-mentioned immunochromatographiassays assays test kit, including such as
Lower step: (1) arranges the adhesive pad of bottom；(2) antibody is fixed film to be bonded on adhesive pad；(3) fix on film at antibody
The anti-first detectable substance antibody of endocyclic area coating；(4) anti-the of outer shroud subregion coating variable concentrations on film is fixed at antibody
Two detectable substance antibody；(5) by predetermined first detectable substance identical with the second detectable substance coloring intensity time, the second detectable substance is anti-
Bulk concentration and the first detectable substance, relative to the first detectable substance and the relation of the concentration of the second detectable substance total amount, are marked in outer shroud subregion
Remember that the first detectable substance is relative to the first detectable substance and the concentration value of the second detectable substance total amount；(6) at described outer shroud dispensing area
Being respectively provided with many sub regions outside each subregion, each sub regions is coated with the anti-second detectable substance antibody of variable concentrations successively,
The anti-second detectable substance antibody concentration of subregion coating be positioned at subregion concentration belonging to it with belonging to it subregional next
Between the concentration of subregion；(7) fix anti-igg linear with the position coating of annular region distance specific range on film at antibody to resist
Body；(8) fixing the side of film at antibody and arrange bed course, it contains the antibody through label labelling；(9) film is fixed at antibody
Opposite side arranges adsorptive pads；(10) side at bed course arranges sample pad；(11) arranged between a circle at internal ring by perforating device
Every aperture, formed tear outlet surround tear out region；(12) tear out area bonded described in and tear shaping, tear shaping energy by described
Enough this is torn out region to tear out from internal ring.
In all documents incorporated by reference the most in this application that the present invention mentions, it is individually recited just as each document
As with reference to like that.In addition, it is to be understood that after the above disclosure having read the present invention, protection scope of the present invention is not
Being limited only to above-described embodiment, the present invention can be made various changes or modifications by those skilled in the art, without departing from the present invention
Under principle premise, these equivalent form of values fall within the application appended claims limited range equally.
Claims (6)
1. an immunochromatographiassays assays test kit, including: adhesive pad, it is arranged at bottom, for gluing with the layer being arranged on
Close；Antibody fixes film, and it is bonded on adhesive pad, and it arranges antibody dispensing area；Bed course, it is arranged at antibody and fixes film
Side, containing the antibody through label labelling；Adsorptive pads, it is arranged at antibody and fixes film opposite side, is used for absorbing unnecessary sample
This；Sample pad, it is arranged at bed course side, fixes film connection side with bed course and antibody relative, be used for receiving sample；Its feature exists
In: described antibody dispensing area is annular region, including internal ring and outer shroud；The district that blocks water is set between described internal ring and outer shroud
Territory；The anti-first detectable substance antibody of described internal ring coating；Described outer shroud is radially divided into the region that multiple area is identical, regional
Between arrange and block water region；Described outer shroud regional is coated with the anti-second detectable substance antibody of variable concentrations successively；Described outer shroud
Regional respectively marker readout, this reading represents dense relative to the first detectable substance and the second detectable substance total amount of the first detectable substance
Degree.
Immunochromatographiassays assays test kit the most according to claim 1, it is characterised in that: described immunochromatographiassays assays test kit
It is not provided with colorimetric card；Sample, after internal ring dispensing area and outer shroud dispensing area react, selects from outer shroud dispensing area
Select the region consistent with the color development signal intensity of internal ring dispensing area, according to the reading in this region determine the first detectable substance relative to
First detectable substance and the concentration of the second detectable substance total amount.
Immune reagent kit the most according to claim 2, it is characterised in that: each point of the dispensing area of described outer shroud is set
The concentration of the anti-second detectable substance antibody in region so that it is in only have the concentration of a subregional anti-second detectable substance antibody corresponding
The first detectable substance be negative relative to the concentration of the first detectable substance and the second detectable substance total amount.
Immunochromatographiassays assays test kit the most according to claim 3, it is characterised in that: each of described outer shroud dispensing area
Being respectively provided with many sub regions outside subregion, each sub regions is coated with the anti-second detectable substance antibody of variable concentrations, sub-district successively
The anti-second detectable substance antibody concentration of territory coating is positioned at subregion concentration belonging to it and next subregion subregional belonging to it
Between the concentration of territory；The region that blocks water is set between described each sub regions；Expression corresponding to described each sub regions respectively labelling the
One detectable substance is relative to the first detectable substance and the reading of the concentration of the second detectable substance total amount.
5., according to the preparation method of the immunochromatographiassays assays test kit one of claim 1-4 Suo Shu, comprise the steps: (1)
The adhesive pad of bottom is set；(2) antibody is fixed film to be bonded on adhesive pad；(3) fix the endocyclic area on film at antibody to be coated with
Cloth resists the first detectable substance antibody；(4) fix anti-second detectable substance of the outer shroud subregion coating variable concentrations on film at antibody to resist
Body；(5) by predetermined first detectable substance identical with the second detectable substance coloring intensity time, the second detectable substance antibody concentration and the
One detectable substance, relative to the first detectable substance and the relation of the concentration of the second detectable substance total amount, detects at outer shroud subregion labelling first
Thing is relative to the first detectable substance and the concentration value of the second detectable substance total amount；(6) in each subregion of described outer shroud dispensing area
Being respectively provided with outward many sub regions, each sub regions is coated with the anti-second detectable substance antibody of variable concentrations successively, and subregion is coated with
Anti-second detectable substance antibody concentration be positioned at subregion concentration belonging to it and next subregion concentration subregional belonging to it
Between；(7) anti-igg antibody linear with the position coating of annular region distance specific range on film is fixed at antibody；(8) anti-
Body is fixed the side of film and is arranged bed course, and it contains the antibody through label labelling；(9) the opposite side setting of film is fixed at antibody
Adsorptive pads；(10) side at bed course arranges sample pad.
6. an immunochromatographiassays assays test kit, including: adhesive pad, it is arranged at bottom, for gluing with the layer being arranged on
Close；Antibody fixes film, and it is bonded on adhesive pad, and it arranges antibody dispensing area；Bed course, it is arranged at antibody and fixes film
Side, containing the antibody through label labelling；Adsorptive pads, it is arranged at antibody and fixes film opposite side, is used for absorbing unnecessary sample
This；Sample pad, it is arranged at bed course side, fixes film connection side with bed course and antibody relative, be used for receiving sample；Its feature exists
In: relatively determine testing result by the first detectable substance and the second detectable substance luminescent chromaticity.
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| CN201610612136.7A CN106290924A (en) | 2016-07-31 | 2016-07-31 | A kind of immunochromatographiassays assays test kit |
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| US20010053531A1 (en) * | 2000-06-14 | 2001-12-20 | Kim Scheuringer | Device for determining a substance contained in a body fluid |
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Application publication date: 20170104 |