• 제목/요약/키워드: I-ELISA

검색결과 409건 처리시간 0.033초

경합 Enzyme-Linked Immunosorbent Assay에 의한 대두 및 대두가공제품 중의 Bowman-Birk Protease Inhibitors의 함량 분석 (Quantification of Bowman-Birk Protease Inhibitors in Soybeans and Soybean Products by Competitive Enzyme-Linked Immunosorbent Assay)

  • 김성란;손동화;김수일;홍희도
    • Applied Biological Chemistry
    • /
    • 제42권4호
    • /
    • pp.310-316
    • /
    • 1999
  • 대두가공제품 중에 존재하는 Bowman-Birk protease inhibitor(BBPI) 함량을 protease 저해활성 측정 및 경합 Enzyme-Linked Immunosorbent Assay(ELISA)로 살펴보았다. 항체제조를 위한 BBPI는 ion exchange chromatography와 전기영동 후 gel slicing 방법으로 시판 soybean trypsin-chymotrypsin inhibitor로부터 순수, 분리하였다. 순수분리한 BBPI를 면역원으로 rabbit anti-BBPI antibody를 조제하였으며 단백질 농도별 titration방법으로 BBP에 비교적 선택적으로 결합하는 항체임을 확인하였다. 이를 이용한 경합 ELISA 방법으로 BBPI를 정량하기 위한 표준 정량곡선을 작성하였으며 시료용액중의 BBPI 함량이 $0.03{\sim}30\;{\mu}g/ml$ 범위일 경우에 정량적인 분석이 가능하였다. 대두품종별 chymotrypsin 저해활성은 $8,462{\sim}12,428\;U/g$이었으며 BBPI 함량은 $482{\sim}692\;mg%$ 이었다. 시판 대두 가공제품 중에서 5종의 콩나물은 건물량 기준으로 $10,695{\sim}13,249\;U/g$의 chymotrypsin 저해활성과 $529{\sim}803\;mg%$의 BBPI 함량을 나타내었으며 일부 두부제품에서도 68.9 mg%정도의 BBPI가 검출되었다. 그 밖의 두유, 된장, 고추장 및 간장 등의 대두발효식품, 탈지대두박 등에서는 chymotrypsin 저해활성 및 BBPI가 거의 검출되지 않았다.

  • PDF

Synthetic Peptide-Based Enzyme-Linked Immunosorbent Assay for Human $\alpha$-Fetoprotein

  • Yoon, Mi-Chung;Lee, Hyun-Hee
    • 대한의생명과학회지
    • /
    • 제7권3호
    • /
    • pp.103-110
    • /
    • 2001
  • $\alpha$-Fetoprotein(AFP) is a good marker for the detection of several diseases such as hepatocellular carcinoma, gonadal germ cell tumor, gastric tumor, and Down's syndrome. In this study, we developed ELISA, using synthetic peptides corresponding to the epitopes of AFP. Five kinds of peptides were synthesized from AFP to produce antibodies in rats that recognize AFP in human plasma as well as amniotic fluid and do not cross-react with serum albumin. All five kinds of antibodies showed good reactivities with their peptide-keyhole limpet hemocyanin conjugates. Anti-synthetic peptide 1 (R-N-E-Y-G-I-A-S-I-L, 4-13) antibody, in particular, reacted well with AEP as well as synthetic peptide 1-KLH but not with human serum albumin. The binding affinity(Kd) was 2.7$\times$10$^{-9}$M for peptide 1 and 6.8$\times$10$^{-8}$M for AEP. The range for measurement of AFP was 10~1,000 ng/ml. The within-assay and between-assay coefficients of variance(CV) were 4.83% and 10.97%, respectively. In a sample of 31 sera and 33 amniotic fluids, there was a good correlation between AFP values determined in this assay and those in a commercial kit. These results indicate that the antibodies against synthetic peptides corresponding to the epitopes of AFP are highly specific to APP and synthetic peptide-based ELISA would be useful for the measurement of human AFP.

  • PDF

항투명대 항체의 특성에 관한 연구 I. 간접효소면역분석법과 간접면역형광분석법에 의한 항투명대 항체의 확인 (Studies on the Characteristics of Anti-Zone Antibody I. Identification of Anti-Zona Antibody by Indirect ELISA and Indirect Immunofluorescence Test)

  • 김은영;유영춘;박세필;정형민;정길생;김종배
    • 한국가축번식학회지
    • /
    • 제14권2호
    • /
    • pp.107-114
    • /
    • 1990
  • These experiments were undertaken as a basic study to develop immunocontraceptive vaccine and to understand the role of zona pellucidae in early fertilization process by identifying the monoclonal and polyclonal antibody to porcine zona pellucidae and polyclonal antibody to mouse zona pellucidae by indirect ELISA and indirect immunofluorescence test. The results obtained in these experiments were summarized as follows : 1. The titer of the antibodies to zona was determined by indirect ELISA using solubilized porcine zona coated plates. Both monoclonal and rabbit polyclonal antibodies showed very high titers ; O.D at 1 : 12,800 dilution of antibodies was still significantly higher than that of non-immunized control serum. Rabbit anti-mouse zona pellucidae sera also reacted with porcine zona pellucidae. 2. By indirect immunofluorescence test strong fluorescences were observed on the egg treated with homologous and heterologous rabbit polyclonal antibodies and FITC lablled 2nd antibodies and found to crossreact strongly with the eggs from the pig and mouse. While weaken fluorescences were observed on the eggs treated with monoclonal antibodies.

  • PDF

Development of an Enzyme-Linked Immunosorbent Assay for the Organophosphorus Insecticide Cyanophos

  • Park, Jae-Hyun;Park, Won-Chul;Kim, Yoo-Jung;Lee, Yong-Tae
    • Bulletin of the Korean Chemical Society
    • /
    • 제23권4호
    • /
    • pp.605-609
    • /
    • 2002
  • A competitive enzyme-linked immunosorbent assay (ELISA) was developed for the quantitative detection of organophosphorus insecticide cyanophos. An analogue (hapten) of cyanophos was synthesized and was coupled to BSA to produce polyclonal antibodi es from rabbits. The antisera were screened against another hapten coupled to ovalbumin (OVA). Using the sera of highest specificity, an antigen-coated ELISA was developed, which showed an I50 of 310 ng/mL with the detection limit of 20 ng/mL. The antibodies showed negligible cross-reactivities with other organophosphorus pesticides except for parathion-methyl, which makes the assay suitable for the selective detection of cyanophos.

Diagnostic Efficacy of a Recombinant Cysteine Protease of Spirometra erinacei Larvae for Serodiagnosis of Sparganosis

  • Rahman, S.M. Mazidur;Kim, Jae-Hwan;Hong, Sung-Tae;Choi, Min-Ho
    • Parasites, Hosts and Diseases
    • /
    • 제52권1호
    • /
    • pp.41-46
    • /
    • 2014
  • The mature domain of a cysteine protease of Spirometra erinacei plerocercoid larva (i.e., sparganum) was expressed in Escherichia coli, and its value as an antigen for the serodiagnosis of sparganosis was investigated. The recombinant protein (rSepCp-1) has the molecular weight of 23.4 kDa, and strongly reacted with the sparganum positive human or mice sera but not with negative sera by immunoblotting. ELISA with rSepCp-1 protein or sparganum crude antigen (SeC) was evaluated for the serodiagnosis of sparganosis using patient's sera. The sensitivity and specificity of ELISA using rSepCp-1 protein were 95.0% (19/20) and 99.1% (111/112), respectively. In contrast, the sensitivity and specificity of ELISA with SeC were 100% (20/20) and 96.4% (108/112), respectively. Moreover, in experimentally infected mice, the sensitivity and specificity of both ELISA assays were 100% for the detection of anti-sparganum IgG. It is suggested that the rSepCp-1 protein-based ELISA could provide a highly sensitive and specific assay for the diagnosis of sparganosis.

SIV의 p27 재조합 단백질을 이용한 SIV 항체 검출을 위한 ELISA의 최적 조건 (Optimalization of ELISA using Recombinant p27 Protein of SIV for Detection of Anti-SIV)

  • 김은옥;김은;오윤이;신광순;김현수;김철중
    • 대한수의학회지
    • /
    • 제42권1호
    • /
    • pp.101-108
    • /
    • 2002
  • SIVmac239 isolate의 p27유전자를 PCR로 증폭하여 pMAL-cri vector에 cloning하였다. 이를 Escherichia coli.에서 발현시켜 정제하여 국내에 수입된 macaque 11마리와 marmoset 21마리의 혈청에서 SIV 항체를 immunoblot으로 검사한 결과 macaque 1마리가 SIV 감염이 의심되었다. 또한 정제된 재조합 단백질을 이용하여 check board system으로 ELISA 방법의 최적 조건을 확립하였다. 정제 p27 항원 200ng/well을 plate에 coating하기에 적합하였고 conjugate는 1:1000으로 희석하는 것이 가장 좋았으며 위의 32 마리의 혈청을 ELISA로 검사한 결과 모두 anti-SIV 음성이었다.

면역측정법을 이용한 식물 홀몬의 분석 I. 옥신(IAA)에 대한 단크론 항체 생산 (Analysis of Plant Hormones by Immunoassay I . Production of Monoclonal Antibodies to Indole- 3-acetic acid)

  • 황태익;임현옥;이재와
    • 한국작물학회지
    • /
    • 제36권6호
    • /
    • pp.506-512
    • /
    • 1991
  • IAA에 대한 단크론 항체를 생산하고 이를 이용하여 생체중의 내생 IAA를 정량분석하기 위해 ELISA를 개발하고 본법을 사용하여 담배 종자 발아중 내생 IAA함량을 정량분석하였다. 그 결과는 1. IAA에 대한 단크론 항체 생산 세포주 3가지를 선발 작성하였으며 이 세포주로부터 생산되는 항체는 모두 IgG$_1$ 타입의 면역 글로블린이었다. 2. 상기 항체를 사용하여 ELISA를 수행하여 표준곡선을 작성하였던 바 검출 한계는 1pmol이었으며 검출 범위는 500pmol이었다 3. 표준곡선으로부터 작성한 Scatchard plot에 의한 친화 상수와 결합상수는 6.7$\times$$10^{-10}$ L/M과 6$\times$$10^{-10}$ L/M이었다. 4. 여러가지 IAA유사물질과 교차반응에 의해서 본 mAb는 특이성이 매우 높고 RIA에 의해서 고역가임을 확인하였다 5. 발아중인 담배종자로부터 면역측정에 의해서 내생 IAA를 정량분석하였다 6. 상기의 결과에 따라서 본 mAb를 이용하여 생체중의 내생 IAA를 간편하게 정밀 분석할 수 있음을 확인하였다.

  • PDF

한국산 겨우살이 렉틴 (KML-C)에 대한 단일크론항체의 생산과 특성 (Production of Monoclonal Antibodies Specific to Korean Mistletoe pectin (KML-C) and Their Characterization)

  • 윤택준;유영춘;강태봉;김성훈;김갑수
    • 약학회지
    • /
    • 제45권2호
    • /
    • pp.180-189
    • /
    • 2001
  • We have reported that water-extracted Korean mistletoe (KM-110) had various biological activities such as antitumor and immunomodulatory activity, and the pectin fraction (KML-C) of the extract was one of major factors related to its biological functions. In this paper, we produced murine monoclonal antibody (mAb) against KML-C. The cAbs obtained were largely classified into two groups according to specificity to KML-C and ML-I, a pectin from European mistletoe. One group mAbs (9H7-D10 and 3C2-lH4) strongly reacted with KML-C, but not ML-I. In contrast, another group cAbs (8Bll-2C5, BE12-3E9 and 5E10-Fl) reacted with both KML-C and ML-1. The subisotypes of these mobs were shown to be IgGl (9H7-lD10, 3C2-lH4 and 8Bll-2C5) or IgM (8E12-3E9 and 5E10-Fl). To develop an assay system for determination of the amount of KML-C, we established the sandwich ELISA (enzyme-linked immunosorbent assay) method using these mAbs and horse radish peroxidase (HRP)-labelled cAbs. In various combinations of the cAbs for coated antibody and detection antibody, the sandwich ELISA quantitatively detected KML-C, showing the detection limit ranging from 7-5,000 ng/ml. Especially reproducibility (C.V) of the sandwich ELISA, in which 8E12-3E9 was used for coating antibody and 8Bll-2C5-HRP for detection antibody, was 4.59-5.83 in intra assay, and 3.9-9.4 in inter assay.

  • PDF

항-AFP 단일클론 항체를 이용한 간암진단 효과의 검토 (Evaluation of Anti-AFP Monoclonal Antibodies as Immunodiagnostic Reagents for Hepatocellular Carcinoma)

  • 현광자;강희갑;강신성
    • 한국동물학회지
    • /
    • 제38권3호
    • /
    • pp.382-387
    • /
    • 1995
  • 항-AFP 단일 클론 항체를 생산한 다음, 이를 이용한 noncompetitive ELISA 방법으로 정상인과 간암 및 그 밖의 간질환 환자의 혈청내 AFP농도를 측정해 본 결과 간암진단 방법으로는 혈청 AFP농도 측정이 필수적임이 확인되었다. 또한 간암 및 그 밖의 간질환 환자의 조직에 대한 항-AFP-항체의 반응성을 immunperoxidase 방법과 indirect immunofluorescence 방법으로 검정해 본 결과, 간암조직세포 및 일부 간질환 조직세포에서 항-AFP-항체에 대해 양성반응을 나타내었다. 그러나 그 반응성의 정도는 간암조직세포에서 보다 간암조직 주위의 비신생 간세퐁서 더욱 높았다. 그러므로 간암 진단에 있어서 AFP항원을 면역조직화학적으로 검정하는 방법은 적합하지 않았다.

  • PDF