JPH1138007A - Agglutinative image judging device - Google Patents

Agglutinative image judging device

Info

Publication number
JPH1138007A
JPH1138007A JP19713497A JP19713497A JPH1138007A JP H1138007 A JPH1138007 A JP H1138007A JP 19713497 A JP19713497 A JP 19713497A JP 19713497 A JP19713497 A JP 19713497A JP H1138007 A JPH1138007 A JP H1138007A
Authority
JP
Japan
Prior art keywords
image
wells
well
agglutination
result
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.)
Pending
Application number
JP19713497A
Other languages
Japanese (ja)
Inventor
Yoshinori Niinai
佳能 二井内
Koji Sato
孝二 佐藤
Hiroyuki Takahashi
廣之 高橋
Sadamoto Tachihara
定幹 立原
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.)
Koki Holdings Co Ltd
Original Assignee
Hitachi Koki Co Ltd
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 Hitachi Koki Co Ltd filed Critical Hitachi Koki Co Ltd
Priority to JP19713497A priority Critical patent/JPH1138007A/en
Publication of JPH1138007A publication Critical patent/JPH1138007A/en
Pending legal-status Critical Current

Links

Landscapes

  • Investigating Or Analysing Materials By Optical Means (AREA)

Abstract

PROBLEM TO BE SOLVED: To immediately recognize and confirm judged results by reading the state of an agglutination reaction with a camera, converting them into electric signals for image processing, and outputting the results and image data as they are with a printing device. SOLUTION: A specimen and a reagent are reacted in the wells of a micro- plate 1' having multiple wells, then the micro-plate 1' is mounted on a tray 6 and quietly thrust into an agglutinative image judging device 5. When setting is completed, the micro-plate 1' is photographed by a CCD camera 7, the signal is sent to an image process section 8, and the degrees of the agglutination reaction in the wells are arithmetically processed via the contrast data of images. The processed data are compared with the known values stored in a controller 9, and they are judged as negative (-), weak positive (±), positive (+), or unjudicable (?). The judged results and image data are outputted to a video printer 10, and they are printed together with inspection items selected in advance. The printed results are printed near well images.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は、粒子凝集判定を自
動で行う凝集像判定装置に関するものある。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an agglutination image determining apparatus for automatically determining agglutination of particles.

【0002】[0002]

【従来の技術】従来の凝集像判定装置は、特公平5−6
5021号公報に開示されているようにカメラからの信
号をコンピュータで画像処理・計算処理することによっ
て、凝集反応の陽性、陰性を判断し、その結果をプリン
トアウトしていた。
2. Description of the Related Art A conventional agglutination image determination apparatus is disclosed in
As disclosed in Japanese Patent No. 5021, a signal from a camera is subjected to image processing and calculation processing by a computer to determine whether the agglutination reaction is positive or negative, and the result is printed out.

【0003】[0003]

【発明が解決しようとする課題】粒子凝集判定方法のマ
イクロタイター法における凝集状態の判定は、通常教育
を受けた検査技師が目視により行っているが、技師間に
おいて個人差が生じたり、判定結果を記載する際に誤記
してしまう恐れがあるという問題を有していた。また、
上記方法とは別に凝集状態を自動で判定し、その結果を
プリントアウトする凝集像判定装置が提供されている。
これにより、個人差や誤記による問題はなくなるが、凝
集状態が微妙な場合には正しい判定を行うことができな
い可能性を有しているため、検査技師による見直しを必
要としていた。しかし、凝集反応は時間と共に変化する
ことからそのもの自体を保管することは難しいことであ
り、また簡便さもあって多数の検査が行われていること
から保管することは非現実的なことであった。そのた
め、判定終了後、滅菌処理を施してから廃棄されてい
る。従って、多くの場合には、見直し時点で既に検体が
存在していないため、再度患者から採血するなどして検
査をしなおすか、または画像データがコンピュータの記
憶媒体に記録されている場合には、そのデータを呼び出
しテレビモニタに映すなどして検査技師が再判定しなけ
ればならなかった。更に、臨床医が患者の抗体価や抗原
価の推移を治療上の判断材料とする際、実際の凝集像を
観察することは難しいことであるから、単なる数値の比
較で判断せざるお得ない状況であった。
The state of aggregation in the microtiter method of the particle aggregation determination method is usually visually inspected by an inspected technician. However, there is a problem that there is a risk of erroneous writing when describing. Also,
In addition to the above-described method, there is provided an agglutination image determination apparatus that automatically determines the aggregation state and prints out the result.
This eliminates the problem due to individual differences and erroneous writing, but when the cohesion state is delicate, there is a possibility that a correct judgment cannot be made, so a review by an inspection technician was required. However, since the agglutination reaction changes with time, it is difficult to store itself, and because of the simplicity, it has been impractical to store it because many tests have been performed. . For this reason, after the determination is completed, it is disposed after sterilization. Therefore, in many cases, the sample does not already exist at the time of the review, and the test is performed again by collecting blood from the patient, or when the image data is recorded on the storage medium of the computer. The technician had to re-determine by calling the data and displaying it on a television monitor. Furthermore, it is difficult for a clinician to observe the actual agglutination image when using a patient's antibody titer or change in antigen titer for therapeutic judgment, so it is inevitable to judge by simple numerical comparison. It was a situation.

【0004】本発明の目的は、上記問題を解消し、判定
した結果と共に画像出力可能な凝集像判定装置を提供す
ることである。
An object of the present invention is to solve the above problem and to provide an aggregated image judging device capable of outputting an image together with the judgment result.

【0005】[0005]

【課題を解決するための手段】上記目的は、凝集反応の
状態をカメラ等で読み取り、電気信号に変えて画像処理
していることを利用し、結果と共に画像データをそのま
ま印刷装置にて出力することにより達成される。
The object of the present invention is to utilize the fact that the state of the agglutination reaction is read by a camera or the like, and image processing is performed by converting the state into an electric signal. This is achieved by:

【0006】[0006]

【発明の実施の形態】図1は本発明になる粒子凝集判定
結果を示す出力例、図2は凝集像判定装置5を示す略構
成図、図3〜図5は他の粒子凝集判定結果を示す出力例
である。図2において、試験項目に合った凝集方法に従
い複数のウェルを持つマイクロプレート(多くは96穴
または120穴)1’のウェル内で検体と試薬を反応さ
せた後、トレイ6に乗せて凝集像判定装置5に静かに押
し込む。マイクロプレート1’の外周部には、マーカー
などで直接或いはテープを貼りその上に検体番号など必
要事項4が書かれている。セットが終了するとCCDカ
メラ7でマイクロプレート1’を撮影し、その信号を画
像処理部8にて送信し、各ウェル内の凝集反応の程度を
画像の明暗データを用いて演算処理する。処理されたデ
ータは制御部9に記憶されている既定値と比較され、そ
れぞれの状況に応じて陰性(−)、弱陽性(±)、陽性
(+)及び異常反応や空の状態の場合に判別不能として
所定のマークとして、例えば(?)と判定する。判定終
了後、上記結果をCCDカメラ7で撮った画像データと
共にビデオプリンタ10に出力し、前もって選択した検
査項目(例えば肝炎の抗体検査の場合、anti−HB
sなど)や測定時刻等と共に印刷する。印刷されたもの
は図1に示すようにマイクロプレートの像1と共に各ウ
ェル像2の近傍に結果3が印字される。当然、前記マイ
クロプレート1’外周に書かれた情報4も印刷されるこ
とから、わざわざ検体番号などの情報を入力する必要も
ない。なお、粒子凝集判定方法には、多検体のふるい分
けに行われる定性試験(スクリーニング)や定性試験で
陽性や保留となった場合に行う確認試験及び検体の抗体
価や抗原価などを調べる定量試験などがある。従って、
それぞれの試験方法に則った判定基準と出力のフォーマ
ットを制御部に記憶させておけば、各ウェルごとの判定
だけではなく複数のウェルを用いて行う各種検査法にあ
った最終結果(終価)まで、同時に印刷することが可能
となる。図3は定性試験の最終結果11を合わせて出力
した一例を示す。図中の検査は1検体に3個のウェルを
用い、中央及び右端のウェル内(左端のウェルは希釈の
際に使用するのみ)で検体と試薬を混和させ判定するも
のであり15検体の検査例である。中央のウェルに対照
血球液、右端(3個目のウェル)のウェルに感作血球液
をそれぞれ検体と混和させ、それぞれの凝集状態によっ
て、最終判定を出す試験方法である。本例の場合の判定
基準は以下の通りであり、通常は前述の通り臨床検査技
師が判断しているが、本発明によれば最終結果11に示
すように結果を自動的に印刷できる。
FIG. 1 is an output example showing a result of particle agglutination determination according to the present invention, FIG. 2 is a schematic configuration diagram showing an agglutination image determination device 5, and FIGS. It is an output example shown. In FIG. 2, a sample and a reagent are allowed to react in a well of a microplate (mostly 96 or 120 wells) 1 'having a plurality of wells according to an agglutination method suitable for a test item, and then placed on a tray 6 for agglutination image. Push it gently into the judgment device 5. Necessary items 4, such as a sample number, are written on the outer periphery of the microplate 1 'directly or with a tape with a marker or the like. When the setting is completed, the microplate 1 'is photographed by the CCD camera 7, the signal is transmitted by the image processing unit 8, and the degree of agglutination reaction in each well is arithmetically processed using the light and dark data of the image. The processed data is compared with a predetermined value stored in the control unit 9, and depending on each situation, a negative (-), a weak positive (±), a positive (+), and an abnormal reaction or empty state For example, (?) Is determined as a predetermined mark that cannot be determined. After the determination is completed, the above result is output to the video printer 10 together with the image data taken by the CCD camera 7, and the inspection items selected in advance (for example, in the case of an antibody test for hepatitis, anti-HB
s) and the measurement time. As shown in FIG. 1, the result 3 is printed near each well image 2 together with the microplate image 1 as shown in FIG. Naturally, since the information 4 written on the outer periphery of the microplate 1 'is also printed, there is no need to input information such as the specimen number. In addition, particle agglutination determination methods include qualitative tests (screening) performed for sieving multiple samples, confirmation tests performed when the qualitative test is positive or suspended, and quantitative tests that examine the antibody titer and antigen titer of the sample. There is. Therefore,
If the control unit stores judgment standards and output formats according to each test method, not only judgment for each well but also final results (final price) for various test methods using a plurality of wells Up to the same time. FIG. 3 shows an example in which the final result 11 of the qualitative test is output together. The test shown in the figure uses three wells for one sample, and mixes the sample and reagent in the center and right wells (the left well is used only for dilution). It is an example. This is a test method in which a control blood cell fluid is mixed in the center well and a sensitized blood cell fluid is mixed with a sample in the rightmost (third well) well, and a final determination is made according to each agglutination state. The determination criteria in this example are as follows, and are usually determined by a clinical laboratory technician as described above. According to the present invention, the result can be automatically printed as shown in the final result 11.

【0007】[0007]

【表1】 [Table 1]

【0008】図4には主に前記定性試験で保留となった
場合に行われる確認試験の最終結果12を合わせて出力
した一例を示す。図4に示す例は6個のウェルを2列使
用し4検体について検査したものであり、上列に検体と
検体希釈液、下列に検体と確認試験液を図中、右側のウ
ェルほど希釈倍率が高くなるよう分注し、更に各ウェル
に定量の感作血球液を加えて混和させたものである。更
に詳しく説明すれば左端のウェルが検体希釈倍率2倍、
2番目のウエルが4倍というように倍々になっており、
右端(6個目のウェル)が64倍となっている。ここ
で、仮にマイクロプレートの横列(左端から6個目ま
で)に25μlの希釈液を入れ、一つ目のウェルに25
μlの検体を入れてよくかき混ぜる。かき混ざった希釈
液と検体から25μl取り出し、右隣の2つ目のウェル
に入れてよくかき混ぜる。更にこのウェルから25μl
取り出し3つ目のウェルに同様に入れる。このような作
業を4つ目、5つ目、6つ目と繰返し行っていくこと
で、右に1つずれるごとに検体の希釈倍率が高くなって
いる。次に同量の試薬を各ウェルに入れ、各ウェルの検
体と試薬の反応を凝集像を見ることによって判定する。
本例の判定基準は上列と下列で陰性に反転するウェルが
何番目かを見てその差が2ウェルより大であると陽性
(検体No.2)、2ウェル以下だと陰性(検体No.
1)である。検体No.3の場合は上列が右端まで陽性
であり、更に希釈倍率をあげても陽性が続く可能性があ
り、この場合、上列と下列の差が2ウェル以上になるこ
とから本試験では判定がつかず保留となった例である。
本例でも図3の場合と同様に最終結果を自動的に印刷で
きる。
FIG. 4 shows an example in which the final result 12 of the confirmation test mainly performed when the qualitative test is suspended is output. In the example shown in FIG. 4, the test was performed on four samples using two rows of six wells. The upper row shows the sample and the sample diluent, and the lower row shows the sample and the test solution. , And a fixed amount of sensitized blood cells was added to each well and mixed. More specifically, the leftmost well has a sample dilution ratio of 2 times,
The second well is doubled, such as four times,
The right end (sixth well) is 64 times. Here, suppose that 25 μl of the diluting solution is temporarily added to the row (from the left end to the sixth) of the microplate, and 25 μl is added to the first well.
Add μl of sample and stir well. Remove 25 μl from the mixed diluent and sample, put into the second well on the right, and mix well. 25 μl from this well
Remove and place in the third well as well. By repeating such operations as the fourth, fifth, and sixth operations, the dilution ratio of the specimen increases each time the operation is shifted to the right by one. Next, the same amount of reagent is put into each well, and the reaction between the sample and the reagent in each well is determined by observing the aggregation image.
The judgment criterion in this example is that the number of wells that are negatively inverted in the upper row and the lower row is positive. If the difference is larger than 2 wells, the result is positive (sample No. 2). .
1). Sample No. In the case of 3, the upper row is positive to the right end, and the positive may continue even if the dilution ratio is further increased. In this case, the difference between the upper row and the lower row becomes 2 or more wells. This is an example of suspension because it was not put on.
Also in this example, the final result can be automatically printed as in the case of FIG.

【0009】図5は定量試験の最終結果13を合わせて
出力した例であり、1列全部のウェル(12個)を使用
し7検体について検査したものである。図5に示す例の
場合、HBs抗体が検体の中にどの程度含まれているか
を調べるものであり、図4と同様、図中右のウェルほど
検体の希釈倍率が高くなっており、陰性に反転した希釈
倍率を求め、これをHBs抗体価とする試験方法であ
る。本例も前記例と同様本発明により自動的に印刷でき
る。なお、図3、図4、図5に示した最終結果11、1
2、13の中で“S”は保留で、更に感度を上げての確
認試験を必要とすることを意味し、“R”は空のウェル
が含まれるなど結果に異常ありと判断し再検査を必要と
することを意味している。
FIG. 5 shows an example in which the final result 13 of the quantitative test is also output, in which seven samples are tested using all the wells (12) in one row. In the case of the example shown in FIG. 5, the amount of HBs antibody contained in the sample is examined. As in FIG. 4, the dilution ratio of the sample is higher in the right well in the figure, and the sample is negative. This is a test method in which an inverted dilution ratio is determined, and this is used as the HBs antibody titer. In this embodiment, printing can be automatically performed according to the present invention as in the above-described embodiment. Note that the final results 11, 1 shown in FIGS.
In "2" and "13", "S" means that the test was suspended and a confirmation test with further increased sensitivity was required. "R" means that the result was abnormal, such as the presence of an empty well. It means that you need.

【0010】[0010]

【発明の効果】本発明によれば、凝集像判定装置で自動
判定した結果を実際の画像と共に出力できるようにした
ので、検査結果に疑問が生じたり見直しの必要が生じた
場合、いつでも実際の凝集反応の状態と判定結果を調べ
ることができる。併せて、最終結果も同時に出力できる
ようにしたので、判定結果を即座に認識でき、且つ確認
することができる。また、抗体価や抗原価の推移を単な
る数値だけではなく凝集画像と共に簡便に見ることがで
きることから、臨床上の治療効果の確認などに役立てる
ことができる。
According to the present invention, the result of the automatic judgment by the agglutination image judging device can be output together with the actual image. Therefore, when the inspection result becomes questionable or needs to be reviewed, the actual result can be obtained at any time. The state of the agglutination reaction and the determination result can be examined. At the same time, the final result can be output at the same time, so that the judgment result can be immediately recognized and confirmed. In addition, since the changes in antibody titer and antigen titer can be easily viewed not only with simple numerical values but also with agglutination images, it can be used for confirmation of clinical therapeutic effects.

【図面の簡単な説明】[Brief description of the drawings]

【図1】 本発明になる粒子凝集判定結果の出力例を示
す状態図である。
FIG. 1 is a state diagram showing an output example of a particle aggregation determination result according to the present invention.

【図2】 本発明になる凝集像判定装置を示す略構成図
である。
FIG. 2 is a schematic configuration diagram illustrating an aggregated image determination device according to the present invention.

【図3】 本発明になる粒子凝集判定結果の他の出力例
を示す状態図である。
FIG. 3 is a state diagram showing another output example of the particle aggregation determination result according to the present invention.

【図4】 本発明になる粒子凝集判定結果の他の出力例
を示す状態図である。
FIG. 4 is a state diagram showing another output example of the particle aggregation determination result according to the present invention.

【図5】 本発明になる粒子凝集判定結果の他の出力例
を示す状態図である。
FIG. 5 is a state diagram showing another output example of the particle aggregation determination result according to the present invention.

【符号の説明】[Explanation of symbols]

1はマイクロプレートの像、1’はマイクロプレート、
2はウエルの像、3は各ウエル毎の判定結果、4はマイ
クロプレート1’の外周に書かれた必要事項、5は凝集
像判定装置、6はトレイ、7はCCDカメラ、8は画像
処理部、9は制御部、10はビデオプリンタ、11、1
2、13は最終結果の印字例である。
1 is a microplate image, 1 'is a microplate,
2 is an image of a well, 3 is a judgment result for each well, 4 is necessary information written on the outer periphery of the microplate 1 ', 5 is an aggregating image judging device, 6 is a tray, 7 is a CCD camera, and 8 is image processing. , 9 a control unit, 10 a video printer, 11, 1
Reference numerals 2 and 13 are print examples of the final result.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 立原 定幹 茨城県ひたちなか市武田1060番地 日立工 機株式会社内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Tadashi Tatehara 1060 Takeda, Hitachinaka-shi, Ibaraki Pref. Hitachi Koki Co., Ltd.

Claims (5)

【特許請求の範囲】[Claims] 【請求項1】 複数のウェルを有するマイクロプレート
の該ウェル内に検体と試薬を混和させ凝集の状態をカメ
ラで撮影し得られる画像信号を処理することで、凝集、
非凝集を判定する凝集像判定装置において、前記カメラ
による画像と共に判定結果を同時に出力することを特徴
とした凝集像判定装置。
An image signal obtained by mixing a specimen and a reagent in a well of a microplate having a plurality of wells and photographing the state of aggregation with a camera to process aggregation,
An agglutination image judging device for judging non-agglutination, wherein the judgment result is output simultaneously with the image from the camera.
【請求項2】 前記各ウェル内の凝集反応状態を自動で
判定し、その結果を前記カメラで取り込んだ画像の中の
それぞれに対応する前記ウェルの近傍に重ねて出力する
ことを特徴とした請求項1記載の凝集像判定装置。
2. The method according to claim 1, wherein an agglutination reaction state in each of the wells is automatically determined, and the result is superimposed and output near the well corresponding to each of the images captured by the camera. Item 3. The aggregation image determination device according to Item 1.
【請求項3】 前記各ウェル内の凝集反応状態の判定結
果において、空のウェル又は異常反応と判定したウェル
に所定のマークを画像と共に出力することを特徴とした
請求項1乃至請求項2記載の凝集像判定装置。
3. The method according to claim 1, wherein a predetermined mark is output together with an image to an empty well or a well determined as an abnormal reaction in the determination result of the agglutination reaction state in each of the wells. Aggregate image determination device.
【請求項4】 複数のウェルを用いて行う検査の最終結
果を前記カメラで取り込んだ画像と共に出力することを
特徴とした請求項1記載の凝集像判定装置。
4. The apparatus according to claim 1, wherein a final result of an inspection performed using a plurality of wells is output together with an image captured by the camera.
【請求項5】 前記出力先がビデオ入力端子を有する印
刷装置であることを特徴とした請求項1又は請求項4記
載の凝集像判定装置。
5. The apparatus according to claim 1, wherein the output destination is a printing apparatus having a video input terminal.
JP19713497A 1997-07-23 1997-07-23 Agglutinative image judging device Pending JPH1138007A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP19713497A JPH1138007A (en) 1997-07-23 1997-07-23 Agglutinative image judging device

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP19713497A JPH1138007A (en) 1997-07-23 1997-07-23 Agglutinative image judging device

Publications (1)

Publication Number Publication Date
JPH1138007A true JPH1138007A (en) 1999-02-12

Family

ID=16369325

Family Applications (1)

Application Number Title Priority Date Filing Date
JP19713497A Pending JPH1138007A (en) 1997-07-23 1997-07-23 Agglutinative image judging device

Country Status (1)

Country Link
JP (1) JPH1138007A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010035530A1 (en) * 2008-09-24 2010-04-01 オリンパス株式会社 Measurement result display method and analysis device
WO2011000944A1 (en) * 2009-07-03 2011-01-06 Vidimsoft Bvba Method for storing and tracing of manual blood typing analyses
JP2019074441A (en) * 2017-10-18 2019-05-16 株式会社島津製作所 Information management device for mass spectrometer

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010035530A1 (en) * 2008-09-24 2010-04-01 オリンパス株式会社 Measurement result display method and analysis device
WO2011000944A1 (en) * 2009-07-03 2011-01-06 Vidimsoft Bvba Method for storing and tracing of manual blood typing analyses
JP2019074441A (en) * 2017-10-18 2019-05-16 株式会社島津製作所 Information management device for mass spectrometer

Similar Documents

Publication Publication Date Title
JP5334643B2 (en) Urine sample analyzer
JP4405600B2 (en) Method and apparatus for calibrating an imaging device for analyzing agglutination reactions
JP2002521660A (en) Agglutination test
JP5591619B2 (en) Urine test apparatus and urine sample measurement result processing apparatus
EP0644414A2 (en) Classification and examination device of particles in fluid
JPH06507969A (en) Fluorophore-assisted carbohydrate electrodynamic diagnostics
US20070223781A1 (en) Method for determining a response of each probe zone on a test strip
US8321142B2 (en) Analyzer, analysis method and computer program product
Hwang et al. Quantitation of low abundant soluble biomarkers using high sensitivity Single Molecule Counting technology
US20100129855A1 (en) Blood cell analyzer, blood cell analyzing method, and computer program product
JPH07104342B2 (en) Method for determining the diagnostic significance of the content of particles in a biological sample containing particles
JP3050046B2 (en) Automatic particle classification system
JP3981445B2 (en) Inspection device
JPH1138007A (en) Agglutinative image judging device
JPH0746112B2 (en) Cell analysis method
EP0684476A1 (en) Titration simulation system and method
JPH09257708A (en) Method and device for deciding test strip
WO1997037219A1 (en) Blood examination analyser, printer for blood examination and reagent cassette imaging apparatus
JP4516802B2 (en) Remote image judgment support system such as electrophoretic examination data
Nakabayashi et al. Evaluation of the automatic fluorescent image analyzer, image titer, for quantitative analysis of antinuclear antibodies
JP3395627B2 (en) Classification method of particle image of living body
JP4611467B2 (en) Diagnosis support system
JPS6159454B2 (en)
JP6657882B2 (en) Inspection system, inspection method, and inspection program
Soepnel A New Zealand based quality assurance programme for the indirect immunofluorescence antinuclear antibody assay onHEp-2/HEp-2000 cells. The first year

Legal Events

Date Code Title Description
A977 Report on retrieval

Free format text: JAPANESE INTERMEDIATE CODE: A971007

Effective date: 20050817

A131 Notification of reasons for refusal

Effective date: 20050830

Free format text: JAPANESE INTERMEDIATE CODE: A131

A02 Decision of refusal

Effective date: 20051227

Free format text: JAPANESE INTERMEDIATE CODE: A02