CN203551564U - Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate - Google Patents

Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate Download PDF

Info

Publication number
CN203551564U
CN203551564U CN201320538617.XU CN201320538617U CN203551564U CN 203551564 U CN203551564 U CN 203551564U CN 201320538617 U CN201320538617 U CN 201320538617U CN 203551564 U CN203551564 U CN 203551564U
Authority
CN
China
Prior art keywords
sample
sampling
elisa
plate
application
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Fee Related
Application number
CN201320538617.XU
Other languages
Chinese (zh)
Inventor
马展
陈黎
张泓
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Shanghai City Children Hospital
Original Assignee
Shanghai City Children Hospital
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Shanghai City Children Hospital filed Critical Shanghai City Children Hospital
Priority to CN201320538617.XU priority Critical patent/CN203551564U/en
Application granted granted Critical
Publication of CN203551564U publication Critical patent/CN203551564U/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

Links

Images

Abstract

The utility model provides a sampling auxiliary system. An enzyme linked immunosorbent assay (ELISA) is widely applied to the detection of antigens or antibodies; a present-stage ELISA is mainly carried out in a manual manner; under the condition that a plurality of projects and a plurality of micro-porous plates are carried out at the same time, a sampling step is complicated, much time is consumed and the error is easy to make, and the sampling speed is slow to cause that the experiment batch is increased and the complexity of experiments is also increased. The sampling auxiliary system comprises a transparent tabletop (3); positions for placing a deep hole diluting plate and a plurality of ELISA plates are integrated above the transparent tabletop (3); a straight ruler (1) capable of sliding on a slide rail (2) is mounted above the ELISA plates; a replaceable lining plate (5) printed with a sampling scheme is arranged below the transparent tabletop. Due to the adoption of the system, the sampling efficiency can be obviously improved; the experiment batch is reduced, the flow is smooth and the sampling error is reduced.

Description

The manual application of sample servicing unit of a kind of enzyme mark microwell plate
Technical field
The utility model relates to a kind of enzyme mark microwell plate plurality of plates carries out the servicing unit of manual application of sample simultaneously, for improving the efficiency of enzyme mark microwell plate loading, and prevents the generation of mistake.
Background technology
Enzyme linked immunosorbent assay (ELISA) is as a kind of method of measuring trace antigen, antibody, sensitive, the special and low cost with it and be widely used in scientific research and clinical assays, especially at clinical medicine clinical labororatory (hospital laboratory), ELISA is extensively carried out as the most conventional technology of immunological test.
ELISA carries out with batch sequential mode conventionally on microwell plate, and its basic process comprises application of sample, and sample is hatched, and washes for the first time version, and version is hatched, washed for the second time to enzyme conjugates, and substrate colour developing, reads the several processes of plate.Although there has been full-automatic instrument to emerge, but due to the intrinsic batch sequence pattern restriction of ELISA, especially when multiple projects, polylith version are carried out simultaneously (this is very common in clinical laboratory's routine work) full-automatic instrument efficiency not high, even also slow than manual in some situation, therefore manual ELISA operation is inevitable.
When multiple projects, polylith version are carried out simultaneously, manual ELISA is a labor intensive, especially application of sample step, sample need be gone in corresponding each hole that joins 96 hole microwell plates one by one, while carrying out multiple projects, plurality of plates at the same time, this work will be loaded down with trivial details and fallibility very; Because the application of sample time is oversize, also will cause that between different holes, excessive the causing between unacceptable hole of incubation time difference makes a variation, and causes the insincere of result simultaneously.
Take common prenatal and postnatal care inspection item (ToRCH) as example, ToRCH comprises altogether 10 projects, take every batch of 92 each samples as example, so just there are 10 blocks of plates, comprise contrast and blank 960 holes altogether, according to normal application of sample speed, within 8-10 minute, add 1 plate meter, for fear of differing from 10 blocks of plates between excessive hole, will have to be divided at least 5 batches, whole application of sample process will consume nearly 2 hours, due to 5 batches, interlock and carry out simultaneously simultaneously, very in a rush of operator, " dead time " that between considering batch, time conflict produces, complete 2 people of whole common needs continuous 4 hours or 1 people uninterruptedly carries out for continuous 7 hours, moreover in the face of 96 orifice plate operations can cause operator's spirit high-pressure, very easily there is application of sample mistake in long-time continuous.
Therefore, improve application of sample speed and prevent application of sample mistake become multiple projects, polylith version carry out simultaneously ELISA measure time significant problem.For the existing solution of this problem, be to use multi-channel loading robot (or claiming liquid working station), by many sample needles, work simultaneously and can make this problem be solved, but the huge volume of multi-channel loading robot and easily prices hundreds thousand of, units up to a million make a lot of laboratories hang back.
Summary of the invention
The utility model provides a kind of enzyme mark microwell plate plurality of plates to carry out the servicing unit of manual application of sample simultaneously, the structure of this device comprises a transparent table top, table top comprises that one is placed the high-rise base plate of microwell plate and the low layer base plate of a placement deep-well plates, the grid of restriction microwell plate position is installed on table top, above microwell plate and high laminate, have a ruler that can slide along slide rail, the below of base plate has one because application of sample scheme is different, can extract liner plate replacement, that be printed on application of sample scheme out.Collaborative by deep-well plates, Multi-channel liquid transfer device, application of sample scheme liner plate, ruler, thereby the speed of application of sample raising loading reduce mistake and realize at the Fast synchronization application of sample that there is no polylith microwell plate under application of sample robot condition when realizing 8-12 hole.
Accompanying drawing explanation
Fig. 1 top view
Fig. 2 front elevation
Fig. 3 side view
The positive middle section figure of Fig. 4
Fig. 5. the part that is printed on the liner plate of application of sample scheme and has amplified
Caption:
1. be arranged on the collimation chi on slide rail (2.)
2. be arranged on the slide rail on the upper lower edge chimb of table top (3.)
3. transparent organic glass table top
4. place the bottom base plate of deep-well plates
5. application of sample scheme liner plate
6. on base plate for the spacing grid of ELISA Plate
7. place the high-rise base plate of normal enzyme target
Embodiment
The design is as shown in the figure: native system main body be the work top made of an organic glass 3., comprise that 4. base plate that 1 not contour transparent organic glass makes (places the low layer base plate of deep-well plates) and 7. with grid, 6. separate 12 plate positions just in time putting into a microwell plate on (the high-rise base plate of placement microwell plate), base plate, wherein 2, the lower right corner holds the deep-well plates of reagent and sample for placing consumption, is lined with a liner plate that is printed on hole number and application of sample scheme 5. under base plate.3. the upper of work top respectively have a slide rail below, and collimation chi two ends 1. can be fixed on slide rail and move horizontally.
Compared with conventional method, the difference of using this device to carry out E LISA test is embodied in the pre-dilution of sample and loading step:
1, sample dilutes in advance:
Because deep-well plates provides the pitch-row identical with multi-channel loading device and microwell plate, while using native system, in the test tube that is diluted in advance deep-well plates rather than routine of sample, carry out.The deep-well plates position that deep-well plates is placed on worktable 4., during original serum application of sample, see through at the bottom of transparent deep-well plates and base plate, the application of sample scheme that 5. printing liner plate is gone up is high-visible, under the indication of liner plate, each hole of microwell plate is indicated by clear, 1. the collimation chi that simultaneously slides arrive that row of application of sample, and under the assisting of collimation chi and application of sample scheme, the possibility that original sample adds wrong hole is greatly diminished.
Because the design of deep-well plates is originally used for keeping sample rather than diluting use, cannot shake and mix, for solving dilution, mix problem, this device should adopt in use and first add the scheme that adds dilution after sample, utilizes dilution and square hole deep hole wooden partition to impact the eddy current producing and completes dilution and mix.
2, the synchronous loading of many plates
Because deep-well plates, ELISA Plate, multi-channel loading utensil have identical pitch-row, therefore in loading link, use multi-channel loading device can once complete the synchronous application of sample in 8-12 hole, loading speed increases several times, because the parallel application of sample of the increase polylith microwell plate of loading speed is achieved, 10 microwell plates can carry out in one batch.The use that simultaneously collimates chi and liner plate can reduce the probability that adds wrong hole greatly.
3, subsequent step
Consistent with traditional E LISA experimental technique.

Claims (2)

1. the manual application of sample servicing unit of enzyme mark microwell plate, collaborative by deep-well plates, Multi-channel liquid transfer device, application of sample scheme liner plate, collimation chi, improve the speed of loading and reduce error rate, the structure of this device comprises a transparent table top, table top comprises that one is placed the high-rise base plate of microwell plate and the low layer base plate of a placement deep-well plates, the grid of restriction microwell plate position is installed on table top, above microwell plate and high laminate, have a ruler that can slide along slide rail, there is a liner plate that is printed on application of sample scheme the below of base plate.
2. the manual application of sample servicing unit of enzyme mark microwell plate according to claim 1, is characterized in that, its liner plate that is printed on application of sample scheme is removable.
CN201320538617.XU 2013-08-30 2013-08-30 Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate Expired - Fee Related CN203551564U (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201320538617.XU CN203551564U (en) 2013-08-30 2013-08-30 Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201320538617.XU CN203551564U (en) 2013-08-30 2013-08-30 Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate

Publications (1)

Publication Number Publication Date
CN203551564U true CN203551564U (en) 2014-04-16

Family

ID=50469661

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201320538617.XU Expired - Fee Related CN203551564U (en) 2013-08-30 2013-08-30 Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate

Country Status (1)

Country Link
CN (1) CN203551564U (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106596993A (en) * 2017-01-25 2017-04-26 浙江中医药大学 Press-type ELISA (enzyme-linked immunosorbent assay) sample loading device
CN108073973A (en) * 2017-11-02 2018-05-25 李宗鲜 A kind of device that can count the colour developing positioning of 96 orifice plates

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN106596993A (en) * 2017-01-25 2017-04-26 浙江中医药大学 Press-type ELISA (enzyme-linked immunosorbent assay) sample loading device
CN108073973A (en) * 2017-11-02 2018-05-25 李宗鲜 A kind of device that can count the colour developing positioning of 96 orifice plates

Similar Documents

Publication Publication Date Title
CN104849468B (en) Detect chemiluminescence protein chip, kit and the detection method of seroglycoid fucose index
CN202204820U (en) Integrated combined kit
CN103743905A (en) Paper chip enzyme-linked immunoassay test card for combined multi-tumor marker test
CN103111340B (en) Sample rack and checkout gear thereof
CN203551564U (en) Manual sample feeding auxiliary device of ELISA (Enzyme Linked Immunosorbent Assay) micro-porous plate
CN204874495U (en) Quick reagent board of appraisal medicine is cultivateed to mycoplasma
CN103941032B (en) A kind of biological sample automatic detecting instrument
CN207081742U (en) A kind of ABO/Rh blood groups diagnose test card
CN103852578B (en) The detachable lath of ELISA Plate
CN203949924U (en) For the biochip of quick magnetic immunoassay
CN204758370U (en) Nitrogen blowing apparatus
CN104655865B (en) Chemiluminescence immunity analyzer incubator
CN213633457U (en) Enzyme linked immunosorbent assay plate and kit for detecting cytokine IL-6
Bacus et al. Quality control in image cytometry: DNA ploidy.
CN205920122U (en) Appearance indicating device on enzyme mark micropore board
US10782288B2 (en) Multi-unit for conducting biochemical test and immunological test and testing method thereof
CN201909753U (en) Glass slide for medical tests
CN106066403A (en) A kind of enzyme mark microwell plate loading instruction device
CN202221285U (en) Detection tool
CN205539021U (en) Lofting board is used to sampling system of sample analysis appearance
CN201804005U (en) Combined type assay test board
CN201179453Y (en) Specimen transferring frame for sifting and checking blood
CN206540922U (en) A kind of PAPP A detection kits
CN105326511B (en) A kind of vacuum blood sampler for immune detection
Lu et al. Development of multiple quantitative fluorescent PCR for rapid diagnosis of common aneuploidy and it's clinical application

Legal Events

Date Code Title Description
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20140416

Termination date: 20140830

EXPY Termination of patent right or utility model