• 제목/요약/키워드: indirect enzyme-linked immunosorbent assay

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돼지에서 분리한 Staphylococcus hyicus subsp hyicus의 protein A (Protein A of Staphylococcus hyicus subsp hyicus isolated from pigs)

  • 김도경;여상건
    • 대한수의학회지
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    • 제30권2호
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    • pp.187-192
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    • 1990
  • 돼지로부터 분리한 Staphylococcus hyicus subsp hyicus 489주의 protein A 존재여부와 함량을 indirect hemagglutination 및 enzyme-linked immunosorbent assay(ELISA)법으로 조사하였다. Indirect hemagglutination text에 의하여 cell-bound protein A 및 extracellular protein A 보유균은 489주 중 각각 87.7% 및 36.0%로 나타났다. ELISA법에 의한 이들 균의 protein A함량 측정에서 전균주의 extracellular protein A는 1ng/ml미만이었으며, cell-bound protein A함량은 대부분의 균주에서 1ng/ml 미만이었고 11주가 25~108ng/ml 수준이었다.

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A Highly Sensitive Indirect Enzyme-Linked Immunosorbent Assay (ELISA) Based on a Monoclonal Antibody Specific to Thermal Stable-Soluble Protein in Pork Fat for the Rapid Detection of Pork Fat Adulterated in Heat-Processed Beef Meatballs

  • Sol-A Kim;Jeong-Eun Lee;Dong-Hyun Kim;Song-min Lee;Hee-Kyeong Yang;Won-Bo Shim
    • 한국축산식품학회지
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    • 제43권6호
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    • pp.989-1001
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    • 2023
  • Processed foods containing pork fat tissue to improve flavor and gain economic benefit may cause severe issues for Muslims, Jews, and vegetarians. This study aimed to develop an indirect enzyme-linked immunosorbent assay (iELISA) based on a monoclonal antibody specific to thermal stable-soluble protein in pork fat tissue and apply it to detect pork fat tissue in heat-processed (autoclave, steam, roast, and fry) beef meatballs. To develop a sensitive iELISA, the optimal sample pre-cooking time, coating conditions, primary and secondary dilution time, and various buffer systems were tested. The change in the iELISA sensitivity with different 96-well microtiter microplates was confirmed. The detection limit of iELISA performed with an appropriate microplate was 0.015% (w/w) pork fat in raw and heat-treated beef. No cross-reactions to other meats or fats were shown. These results mean that the iELISA can be used as an analytical method to detect trace amounts of pork fat mixed in beef.

보르나 바이러스를 실험감염시킨 동물에서 항체검출에 대한 세포효소면역반응법의 평가에 대한 연구 (Evaluation of a cell enzyme-linked immunosorbent assay for the detection of Borna disease virus antibodies in experimentally infected animals)

  • 이두식
    • 대한수의학회지
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    • 제32권3호
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    • pp.377-380
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    • 1992
  • 보르나병 바이러스 혈청학적 진단법에 있어서 새로 개발된 세포효소면역법의 항체검출에 대한 평가를 위하여 지금까지 주로 사용되어진 간접형광항체법과 네 종류의 실험동물에서 서로 비교하였다. 모든 동물에서 간접형광항체법의 역가와 세포효소면역반응치 사이에 상관계수가 모두 0.8 이상으로 고도의 유의성이 인정되었고 두 진단법의 일치율은 한 희석단계 이하로서 재현성이 아주 좋았다. 세포효소면역반응법은 보르나병 바이러스의 혈청역학적 조사 및 병인기전 연구에 유용하게 이용될 수 있을 것으로 생각된다.

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초유에 함유되어 있는 면역조절물질인 MIEF가 B 세포의 분화에 미치는 영향 (Induction of B Lymphocyte Differentiation by a Colostral Immunomodulatory Protein MIEF)

  • 이종호;이종길;한성순
    • 약학회지
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    • 제38권3호
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    • pp.351-357
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    • 1994
  • The levels of maternal immunity enhancing factor(MIEF), which is an immunomodulatory protein identified from bovine colostrum, were determined by indirect competitive enzyme-linked immunosorbent assay(ELISA) for the colostrum and normal milk collected during the first two weeks of lactation. The mean concentration of MIEF in the colostrum of the first day of lactation was $109\;{\mu}g/ml$, and fell from the third day of lactation to $3{\sim}4\;{\mu}g/ml$. The molecular weight of the purified MIEF determined by reducing SDS-PAGE and TSK G2000SW column chromatography was 22,000 and 24,000 daltons, respectively, showing that MIEF is a monomeric peptide in its native form. To examine the capacity of MIEF to induce differentiation of B Lymphocytes, human tonsillar Iymphocytes were cultured in the presence of different concentrations of MIEF, and then antibody secreting cells were enumerated by enzyme-linked immunospot(ELISPOT) assay. When added to cultures of human tonsillar Lymphocytes, MIEF induced differentiation of resting B Iymphocyte to antibody secreting plasma cells as efficiently as LPS.

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Diagnosis of Cylindrocarpon destructans Using Enzyme-Linked Immunosorbent Assay

  • Li, Taiying;Ji, Sungyeon;Jung, Boknam;Kim, Bo Yeon;Lee, Kwang Sik;Seo, Mun Won;Lee, Sung Woo;Lee, Jungkwan;Lee, Seung-Ho
    • 식물병연구
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    • 제25권3호
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    • pp.131-135
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    • 2019
  • Cylindrocarpon destructans causes ginseng root rot and produces radicicol that has an antifungal effect. In this study, we developed a method to detect this fungus using enzyme-linked immunosorbent assay (ELISA). Secreted proteins of C. destructans were used as antigens to obtain C. destructans-specific IgG from mouse. Out of 318 monoclonal antibodies generated from mouse, two antibodies (Cd7-2-2 and Cd7-2-10) showed highest specificity and sensitivity. Indirect ELISA using both antigens successfully detected C. destructans in soils, but direct ELISA using IgG conjugated with horseradish peroxidase failed to detect antigens in soils. The indirect ELISA developed here can efficiently detect the fungus and help manage ginseng root rot disease in fields.

Enzyme-linked Immunosorbent Assay for the Detection of Hen's Egg Proteins in Processed Foods

  • Shon, Dong-Hwa;Kim, Hyun-Jung;Kim, Soo-Ho;Kwak, Bo-Yeon
    • 한국축산식품학회지
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    • 제30권1호
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    • pp.36-41
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    • 2010
  • The Hen's egg is widely used in many processed foods as an ingredient and is one of the most prevalent food allergens in children. To detect egg proteins in processed foods, we developed a competitive indirect enzyme-linked immunosorbent assay (ciELISA) using an anti-ovomucoid (OM) antibody, which was produced by immunization of rabbits with OM, the most heat-stable component of the egg proteins. The detection limit of this quantitative assay system was 30 ng/mL. Cross-reactivity of the anti-OM antibody toward OM, ovalbumin, skim milk, casein, whey protein isolate, and isolated soy protein was 100, 0.4, 0.2, 0.04, 0, and 0%, respectively. In the spike test of egg white powder in milk replacer, commercial sausage, and in-house sausage, the assay recoveries ($mean{\pm}SD$) were $129{\pm}13.7%$, $73.9{\pm}12.5%$, and $65.5{\pm}13.6%$, respectively. When egg white in a commercial crab meat analog and sausage was determined by ciELISA, the assay recovery was found to be 108% and 127%, respectively. The combined results of this study indicate that this novel ciELISA for OM detection could be applied for the quantification of hen's egg proteins in processed foods.

Improvement of indirect enzyme-linked immunosorbent assay for detection of Japanese encephalitis virus antibodies in swine sera

  • Yang, Dong-Kun;Kim, Ha-Hyun;Jo, Hyun-Ye;Lee, Seung Heon;Jang, Sang-Ho;Lee, Sang-Oh;Choi, Sung-Suk;Cho, In-Soo
    • 대한수의학회지
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    • 제57권1호
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    • pp.31-36
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    • 2017
  • Japanese encephalitis (JE) is an important zoonosis caused by the mosquito-transmitted JE virus (JEV), which is a causative agent of reproductive failure in pregnant sows. Detection of JEV antibodies in swine is performed by hemagglutination inhibition (HI), virus neutralization (VN), and the plaque reduction neutralization test (PRNT). The most stringent PRNT is the 90% endpoint PRNT ($PRNT_{90}$). These conventional assays are difficult to carry out in diagnostic laboratories with insufficient instruments or cell culture systems. An alternative assay that is easily conducted and time efficient is required. In this study, we improved the indirect enzyme-linked immunosorbent assay (I-ELISA) with clarified antigen for the detection of JEV antibodies. The I-ELISA results obtained from 175 swine serum samples were compared with HI, VN, and $PRNT_{90}$ results. The sensitivity of I-ELISA was 91.8%, 95.0%, and 94.7% compared with HI, VN, and $PRNT_{90}$ results, respectively. The specificity of I-ELISA was 92.2%, 94.7%, and 94.7% compared with HI, VN, and $PRNT_{90}$ results, respectively. Moreover, the I-ELISA results were significantly correlated with the HI (r = 0.93), VN (r = 0.95), and $PRNT_{90}$ (r = 0.92) results. These results suggest that the improved I-ELISA is useful for serosurveillance of JEV in swine.

옥수수 중의 Zearalenone 분석을 위한 효소번역측정법 (Enzyme-Linked Immunosorbent Assay for Zearalenone in Corn)

  • 손동화;한성민;임선희;이인원;강신영
    • 한국미생물·생명공학회지
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    • 제22권4호
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    • pp.430-435
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    • 1994
  • In order to develop an enzyme-linked immunosorbent assay (ELISA) for zearalenone (ZEA) in corn, we produced antisera by immunizing rabbits with ZEA-6'-carboxymethyloxime-BSA, purified polyclonal anti ZEA antibodies, and subsequently established a competitive indirect ELISA. The antibodies showed low cross-reactivity of 9.6~1.4% against ZEA analogues such as $\alpha$-zearalenol, $\beta$-zearalenol, $\alpha$-zearalanol, and $\beta$-zearalanol. From the standard curve of the ELISA for ZEA in corn, the detection range was found to be 0.3~1, 000 ng/ml. When artificially contaminated corns were assayed by the ELISA, the average recovery of ZEA spiked to 30~1, 000 ng/g was 109% (96~123%), although that of ZEA spiked to 10 ng/g was somewhat high (258%). The average coefficient of variation (CV) of the recovery was 18.0% (0.9~28.3%). When 9 corn samples naturally contaminated were assayed 3 times, the average CV of the determinitions was 27.7% (9.3~52.4%). Therefore, the ELISA was elucidated to be a practical tool for the detection of ZEA of 30 ng/g and more from corn.

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잔류 Chloramphenicol 검사용 효소 면역측정법의 개발에 관한 연구 (Study on Development of Enzyme-Linked Immunosorbent Assay for the Screening of Chloramphenicol Residues)

  • 윤동호;이문한
    • 한국식품위생안전성학회지
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    • 제8권4호
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    • pp.205-214
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    • 1993
  • The monoclonal antibody to chloramphenicol(CAP) was produced to develop an enzyme-linked immunosorbent assay(ELISA) for residual CAP. An immunogen(CAP-BSA) was prepared by immunogen, antibody titer was measured by indirect ELISA. Spleen cells form the immunized mouse were fused with SP2/OAg14 myeloma cells. Among hybridomas selected in HAT media, 6 clones shown high antibody titer to CAP were subjected to cloning by limit dilution, and all of the monoclonal antibodies(MCA1, 2, 3, 4, 5, 7 and 9) produced by each clone were identified as IgG1 by ELISA isotyping analysis. Competitive ELISA condition was established by using the purified monoclonal antibody MCA1 as primary antibody and CAP-HSA conjugate as coating antigen. Standard curve of CAP(n=28) showed that the lowest detection limit of CAP is 20ng/ml level. The cross-reactivities of the 6 monoclonal antibodies showed that CAP sodium succinate. CAP base, P-nitrophenol, and p-nitrobenzyl alcohol were 89∼178, 0.050∼2.237, 0.056∼0.794 and 0.013∼7.939%, respectively. No cross-reactivities were observed with phenylalanine, tyrosine, glutamine, thiamphenicol, neomycin, streptomycin, gentamicin, sulfamethazine, sulfathiazole, chlortetracycline and p-aminobenzoic acid.

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뇌낭미충증의 혈청학적 진단에 있어서 간접 형광항체 반응 및 효소연결성 면역흡착 검사의 비교 평가 (Comparative evaluation of indirect immunofluorescent antibody test with enzyme-linked immunosorbent assay in serodiagnosis of human neurocysticercosls)

  • 엄기선;조승열;임한종
    • Parasites, Hosts and Diseases
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    • 제26권1호
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    • pp.27-32
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    • 1988
  • 뇌낭미충증의 면역혈청학적 진단에 있어서 간접 형광항체 법의 유용성을 평가하기 위하여 효소연결성 면역홉착 검사와 비교 검토하였다. 검사대상자는 확진된 뇌낭미충증 환자의 혈청 163예, 다른 뇌신경 증상 환자, 조층 및 흡충류 감염자 101예 및 건강인 대조군 100예로서 모두 364예이었다. 간점 형광항체 반응에는 인체 유구낭미충의 낭벽 항원을, 효소연결성 면역흡착 검사에는 낭액 항원을 사용하여 혈청내 특이 IgG 항체를 조사한 결과 두 방법간의 민감도 및 특이도에 큰 차이가 없었으며, 양성 및 음성의 동일한 힐청을 검사하였을 때 낭미충증 혈청의 90.8%가 서로 합치되어 밀접한 연관성을 나타내었다. 또한 장내 조충 감염증의 경우 두 방법 모두에서 높은 교차반응을 나타내었으나 간접 형광항체반응의 특이성이 더 좋았으며 특히 간접 형광항체 반응은 흡충류 감염자 혈청에서 교차반응을 나타내지 않았다. 이와 같은 결과는 혈청만을 사용하였을 경우 간접 형광항체반응의 민감도나 특이도가 효소연결성 면역홉착 검사와 차이가 없으며 뇌낭미충증의 진단에 매우 유용함을 나타내고 있었다.

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