• Biotechnology and Bioprocess Engineering:BBE
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• 제4권1호
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• pp.63-65
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• 1999

Although many pharmaceutically useful proteins are produced in E. coli expression system, it is very are rare for the system to be used in the production of diagnostic antigen due to a major problem, i.e., false-positive reaction of e. coli host-derived proteins contaminating purified diagnostic antigen with human sera. The N (nucleocapsid) protein of Seoul virus causing haemorrhagic fever with renal syndrome (HFRS) was produced in E. coli BL21 (DE3), and used for the detection of N protein-specific antibodies in human sera. Using the N protein as a diagnostic antigen of HFRS, the false-positive reaction was cleared by merely mixing the test sera with the extract of E. coli host strain not harboring expression plasmid.

• 분석과학
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• 제35권6호
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• pp.242-248
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• 2022

Luminol 혹은 Bluestar가 혈액 및 표백제와 반응할 때 ethylenediamine (EDA)이 미치는 영향에 대해 연구하였다. 이를 위해 거름종이에 혈액, 염소계 표백제, 산소계 표백제를 묻힌 후 EDA를 첨가한 luminol 혹은 Bluestar로 처리한 후 화학발광의 세기 변화를 관찰하였다. 그 결과 EDA의 농도를 증가시켜도 luminol (혹은 Bluestar)-혈액 반응의 화학발광 세기는 변하지 않는다는 것을 알 수 있었다. 그러나 EDA의 농도가 증가할수록 luminol (혹은 Bluestar)-염소계 표백제 반응의 화학발광 세기는 감소하였고, luminol (혹은 Bluestar)-산소계 표백제 반응의 화학발광 세기는 증가하는 현상이 관찰되었다. 이를 통해 luminol (혹은 Bluestar)로 혈액 검출 시약을 제조할 때 EDA를 첨가할 경우, EDA는 염소계 표백제에 의해 유발되는 위양성 반응을 억제하고 산소계 표백제의 위양성 반응을 유발한다는 것을 알 수 있었다. 이런 점을 종합해서 판단할때 luminol이나 Bluestar로 혈액을증강할 때 EDA를 첨가하는것은 적절하지 않다.

• BMB Reports
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• 제35권2호
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• pp.248-250
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• 2002

Discrimination between the amplification of mRNA and contaminating genomic DNA is a common problem when performing a reverse transcriptase-polymerase chain reaction (RT-PCR). Even after treatment of the samples with DNAse, it is possible that negative controls (samples in which no reverse transcriptase was added) will give positive results. This indicates that there was amplification of DNA, which was not generated during the reverse transcriptase step. The possibility exists that Taq DNA polymerase acts as a reverse transcriptase, generating cDNA from RNA during the PCR step. In order to test this hypothesis, we incubated samples with a DNAse-free RNAse after the cDNA synthesis. Comparison of the results that were obtained from these samples (incubated with or without DNAse-free RNAse) confirms that the reverse transcriptase activity of Taq DNA polymerase I is a possible source of false positive results when performing RT-PCR from intronless genes. Moreover, we describe here a simple and rapid method to overcome the false positive results that originate by this activity of Taq polymerase.

• 한국융합학회논문지
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• 제11권10호
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• pp.139-146
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• 2020

Kastle-Meyer (KM) test는 현장에서 잠재혈흔을 확인하는 예비검사 방법으로, 다른 방법에 비해 감도가 뛰어난 반면, 혈액이 존재하지 않는 곳에서도 위양성 반응이 나타날 수 있다. 본 연구에서는 이러한 KM test의 위양성 반응의 문제를 해결하기 위해 새로운 적용 방법을 제시하고자 하였다. 새로운 KM test 적용 방법의 효과와 위양성의 식별 가능성을 확인하기 위해 기존의 두 가지 KM test 적용 방법과 반응 시간 및 양상을 비교하였다. 실험 결과, 실험에 사용된 KM test 적용 방법 간의 감도에는 유의한 차이가 없었으며, 희석비율이 5000:1 이하인 혈액에서는 즉시 양성반응이 나타나 위양성과 구분하기 용이했다. 하지만 혈액의 희석비율이 높아질수록 양성 반응의 발현 시간이 늦어지면서 위양성과 구분하기 어려웠고, 새로운 KM test 적용 방법은 반응의 양상을 통해 이를 보완할 수 있었다. 따라서 본 연구는 KM test가 현장에서 보다 정확하게 사용될 수 있도록 새로운 적용 방법을 제시하였다.

• 대한의용생체공학회:의공학회지
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• 제18권4호
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• pp.485-491
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• 1997

본 논문은 각성상태에 다른 생리신호와 행위신호 및 주관적 평가의 상관관계에 대하여 나타내었다. Nz와 반응시간은 mKSS level 의 변화와 동일한 경향을 나타내는데 반하여 1분당 눈 깜박임 수는 앞의 두 가지 변수와 다른 경향을 나타내었다. 1분당 눈깜박임 수는 mKSS level 1에서 5까지는 낮은 변화율 갖고 mKSS level 7에서는 높은 변화율을 갖는 반면에 mKSS level 9에서는 이와 반대로 변화율이 급격히 감소한다. 피검자들은 서로다른 1분당 눈깜박임 수(EBR)를 가지나 EBR의 변화율은 비슷하였다. 그러므로 EBR의 변화율을 각성판정지표로 사용할 수 있음을 알 수 있었다. 반응시간 실험 결과로부터mKSS level 5이상부터 작업수행능력이 낮아짐을 알 수 있었고 false positive 와 false negative 가 mKSS level3부터 관찰되었으므로 효과적으로 각성제어를 위하여 mKSS level 3과 5사이에 각성상태를 향상시키기 위한 소리나 향기 등의 자극을 주어야 함을 알 수 있었다.

• 한국수의병리학회지
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• 제7권1호
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• pp.11-15
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• 2003

Antigen retrieval (AR) techniques were widely used to recover the antigenicity from the fixed tissues, which were guided by the philosophy of rendering immunohistochemistry (IHC) applicable to routine formalin-fixed, paraffin-embedded tissues for wide application of IHC in research and clinical filed for morphological observation like as anatomy, histology and pathology. Protease antigen recovery (PAR) is an AR technique, which is obtained the antigen retrieve by using enzyme digestion, and commonly used in IHC field. However, during the IHC for the detection of ovine herpesvirus 2 (OvHV-2) antigen, we noted lymphocyte-like cells-specific staining in the infiltrated cells into various organs like as liver and kidney, which was also shown in the IHC tissues with isotype control. However, those signals were not observed in the tissues conducted with in situ hybridization. Therefore, we analyzed the specificity of the IHC detection results. We found that PAR may induce false-positive result during IHC in lymphocyte-like cells, which were infiltrated mainly around vessels and in interstitial tissues. Through the Phenotyping, we realized that those false-positive cells were B-cell-related cells. These results suggest that PAR, a AR using protease, may induce non-specific false-positive reactions during IHC.

• 한국어병학회지
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• 제21권3호
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• pp.181-188
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• 2008

Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay was used to detect and identify four fish viruses, fish iridovirus, viral hemorrhagic septicaemia virus (VHSV), viral nervous necrosis virus (VNNV), hirame rhabdovirus (HRV). Four viruses were detected by PCR with each specific primers. Identification of iridovirus was achieved by digesting the PCR amplified fragment with a restriction enzyme ApaⅠ. It was possible to distinguish positive from false positive PCR amplicons of VHSV by RFLP of PstⅠ or HindⅢ restriction enzymes. VNNV was identified using RFLP of BamHⅠrestriction enzyme and HRV was identified by XbaⅠ restriction enzyme. This approach can be used for more rapid, simple and specific diagnosis of fish viral diseases.

• 대한임상검사과학회지
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• 제44권3호
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• pp.124-127
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• 2012

Syphilis is an infectious and sexually transmitted chronic disease caused by Treponema pallidum. On the basis of clinical findings, the disease has been divided into a series of overlapping stages, which are used to help guide treatment and follow-up. Persons who have syphilis might seek treatment for signs or symptoms of primary infection, secondary infection and tertiary infection. Latent infections are detected by serologic testing. A presumptive diagnosis of syphilis is possible with the use of two types of serologic tests: nontreponemal tests and treponemal tests assay. The use of only one type of serologic test is insufficient for diagnosis, because each type of test has limitations, including the possibility of false-positive test results in persons without syphilis. KFDA published Koreans guideline of Sexually transmitted infections in 2011. Two hundred samples were tested by RPR card test and Mediace RPR test with simultaneously. The agreement between RPR card test and Mediace RPR test was 95%, the discrepant samples was 5%. The characteristics of 10 discrepant samples was RPR card Positive and Mediace RPR negative nine samples, RPR card negative and Mediace RPR positive one sample. The nine samples were confirmed as FTA-ABS by KFDA guideline of syphilis test algorism, all IgM test was Negative, all IgG test was reactive. So, these cases were past or latent syphilis. The one sample was false-positive reaction.

• 대한의생명과학회지
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• 제27권4호
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• pp.283-290
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• 2021

Severe acute respiratory syndrome coronavirus (SARS-CoV2) is a major coronavirus that infects humans with human Coronavirus (HuCoV)-229E, HCoV-OC43, HCoV-HKU1, HCoV-NL63, Severe acute respiratory syndrome coronavirus (SARS-CoV) and Middle east respiratory syndrome coronavirus (MERS-CoV). SARS-CoV2 is currently a global pandemic pathogen. In this study, we developed conventional RT-PCR based diagnostic system for the detection of SARS-CoV2 which is relatively inexpensive but has high stability and a wide range of users. Three conventional RT-PCR primer sets capable of forming specific band sizes by targeting the ORF1ab [232 nucleotide (nt)], E (200 nt) and N (288 nt) genes of SARS-CoV2 were developed, respectively, and it were confirmed to be about 10~100 times higher detection sensitivity than the previously reported methods. In addition, a standard positive control that can generate specific amplicons by reacting with the developed RT-PCR primers and verify the false-positiv from contamination of the laboratory was produced. Therefore, the diagnostic system that uses the RT-PCR method is expected to be used to detect SARS-CoV2.

• Journal of Yeungnam Medical Science
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• 제5권2호
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• pp.47-52
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• 1988

1988년 8월초부터 9월말동안 영남의료원 내과를 내원한 사람중 1304명에서 대변도말검사를 실시하였으며, 이중 443명에서는 간흡충증 피내반응검사를 하였고, 간흡충증이 의심되는 79명에 대해서는 집란법을 동시에 시행하여 간흡충증을 조사한 결과 다음과 같은 결과를 얻었다. 1) 간흡충 감염율은 3.8%였다. 2) 간흡충증 피내반응검사의 감수성은 82.1%(32/39명)이었고, 특이성은 64.6%(261/404명)이었다. 3) 도말검사상 음성이었으나 피내반응검사가 양성이면서 간흡충증이 의심되거나, 양 검사 모두 음성이나 말초 호산구성 세포의 증가로 간흡충증이 의심되는 사람 79명을 집란법으로 조사한 결과 79명중 16명에서 간흡충란이 발견되었다. 4) 도말검사상 음성이었으나 집란법으로 충란이 발견된 16명중 13명은 경감염이었고 3명은 중등감염된 것으로 나타났다. 이상의 결과에서 간흡충증이 의심되는 환자에게는 반드시 대변도말검사와 함께 피내반응검사를 실시하고 필요시 집란법으로 EPG와 EPD을 조사한 후 확진하여 치료하는 것이 바람직하리라 생각된다.