Double Antibody(이중항체)란 무엇입니까?
Double Antibody 이중항체 - We hypothesized that the strategy of double antibody-conjugated iron oxide nanoparticles which simultaneously target AFP and GPC3 antigens may potentially be used to overcome the tumor heterogeneity and enhance the detection rate for MRI-based MHCC diagnosis. [1] Objective To explore the effect of different doses of atorvastatin calcium combined with double antibody on the recovery of neurological function in patients with acute cerebral infarction. [2]우리는 AFP와 GPC3 항원을 동시에 표적으로 하는 이중항체 결합 산화철 나노입자의 전략이 잠재적으로 종양 이질성을 극복하고 MRI 기반 MHCC 진단을 위한 검출률을 향상시키는 데 사용될 수 있다는 가설을 세웠다. [1] 목적 급성 뇌경색 환자의 신경 기능 회복에 대한 이중 항체와 결합된 아토르바스타틴 칼슘의 다양한 용량의 효과를 조사합니다. [2]
sandwich enzyme linked 샌드위치 효소 연결
The immunohistochemistry, double antibody sandwich enzyme-linked immunosorbent assay (ELISA) and enzyme labeling were used to determine the expression levels of NF-κB P65, IL-6, and NO in the subjects. [1] Collected samples were analyzed by Double Antibody Sandwich Enzyme Linked Immunosorbent Assay (DAS–ELISA) for detection CPMMV. [2] Leaf samples from 2090 trees showing and not showing virus-like symptoms were tested by double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) for PDV infection. [3] Collected samples were analyzed by Double Antibody Sandwich Enzyme Linked Immunosorbent Assay (DAS–ELISA) for detection CPMMV. [4] The Bone Glaprotein (BGP), hematocrit (Hct), alkaline phosphatase (ALP), matrix metalloproteinase-3 (MMP-3), CRP and TNF-α were detected by double antibody sandwich enzyme-linked immunosorbent assay. [5] Human PTX3 concentration was measured with a commercially available ELISA kit, using a double antibody sandwich enzyme-linked immunosorbent assay. [6] Samples were tested for MLN causing viruses by Double Antibody Sandwich Enzyme-Linked Immunosorbent Assay (DAS-ELISA) and Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR). [7] Here, we demonstrated that SCMV strain FZ1 can systemically infect Brachypodium distachyon inbred line Bd21 and Nicotiana benthamiana through inoculation, double antibody sandwich enzyme-linked immunosorbent, transmission electron microscopy, and reverse transcription PCR assays. [8] Testing the collected samples for the presence of turnip mosaic virus (TuMV) by double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) and reverse transcription-polymerase chain reaction (RT-PCR) confirmed that 117 samples were infected with TuMV. [9] BYDV-PAV ve BYDV-MAV’in varligi DAS-ELISA (Double antibody sandwich enzyme linked immunosorbent assay) test yontemi ile belirlenmistir. [10] Double antibody sandwich enzyme-linked immunosorbent assay (ELISA) was used to determine the expression levels of IL-10 and G-CSF in serum before and after treatment. [11] Seven pumpkin plants with typical mosaic symptoms were tested by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) using antibodies for cucumber mosaic virus (Agdia, Elkhart, IN) and squash mosaic virus (Agdia), respectively. [12] The expression of IL-6, IL-10, IL-17, NSE and S100β in peripheral blood of children in each group were detected by double antibody sandwich enzyme-linked immunosorbent assay (ELISA). [13] Obtained antibodies were evaluated using Double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), and Immune Dot-Blot assay. [14] The presence of CatMV in collected samples was tested by double antibody sandwich enzyme linked immunosorbent assay and was confirmed by reverse transcription polymerase chain reaction using specific primers. [15] The serum levels of serum creatinine( SCr),urea nitrogen( BUN),plasma endotoxin level,24 h urinary protein and D-lactate in the plasma were determined by sarcosine oxidase,urease method,tal reagent method,bromo cresol chloroform method and double antibody sandwich enzyme-linked immunoadsorbent assay,respectively. [16] Samples were analysed in Laboratory of Rwanda Agriculture Board, using Double Antibody Sandwich Enzyme Linked Immuno Sorbent Assay. [17] The serum IMA level was detected by double antibody sandwich enzyme-linked immunosorbent assay (ELISA), and the plasma D-D level was detected by immunoturbidimetry. [18] Toplanan ornekler double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) yontemi ile TuMV’nin varliginin belirlenmesi amaci ile testlenmistir. [19]면역 조직 화학, 이중 항체 샌드위치 효소 결합 면역 흡착 분석(ELISA) 및 효소 표지를 사용하여 대상체에서 NF-κB P65, IL-6 및 NO의 발현 수준을 결정했습니다. [1] 수집된 샘플을 CPMMV 검출을 위해 DAS-ELISA(Double Antibody Sandwich Enzyme Linked Immunosorbent Assay)로 분석했습니다. [2] nan [3] nan [4] nan [5] nan [6] nan [7] nan [8] nan [9] nan [10] nan [11] nan [12] nan [13] nan [14] nan [15] nan [16] nan [17] nan [18] nan [19]
enzyme linked immunosorbent 효소결합면역흡착제
Serum IL-38 was measured by double antibody enzyme-linked immunosorbent assays (ELISA). [1] The serum levels of TSH, Lp-PLA2, TNF-α and IL-6 were measured by up-converting phoshor assay and enzyme - linked immunosorbent assay with double antibody sandwich. [2] During survey 150 samples were collected and tested through DASELISA (Double Antibody Sandwiched Enzyme Linked Immunosorbent Assay). [3] A sensitive and specific enzyme-linked immunosorbent assay (ELISA) for the detection of Somatostatin based on double antibody sandwich method was studied in this paper. [4]혈청 IL-38은 이중 항체 효소 결합 면역흡착 분석법(ELISA)으로 측정하였다. [1] TSH, Lp-PLA2, TNF-α 및 IL-6의 혈청 수준은 이중 항체 샌드위치를 사용한 상향 변환 인광 분석 및 효소 결합 면역흡착 분석에 의해 측정되었습니다. [2] nan [3] nan [4]
double antibody sandwich 이중항체 샌드위치
The levels of MCP-4, IL-25, TNF-α and CysLTR-1 in BALF of children in experimental group were determined by double antibody sandwich ELISA. [1] In this work, the surface-enhanced Raman scattering (SERS) detection platform combined with double antibody sandwich method was used to quantitatively detect PCT in serum of patients with PROM. [2] A total of 18 symptomatic plants were collected from nine shallot fields and tested by double antibody sandwich ELISA kit for SVX (DSMZ RT-1042) and TAS-ELISA kit (DSMZ RT-0514-0512/1) for SLV. [3] By the smart design, this work removes a series of conditionality issues of traditional double antibody sandwich-based ICTs and can give a new application direction for 2D nanosheet materials in the rapid detection field. [4] A sensitive and specific double‐antibody sandwich enzyme‐linked immunosorbent assay for the detection of C‐peptide based on double antibody sandwich method was studied in this paper. [5] The immunohistochemistry, double antibody sandwich enzyme-linked immunosorbent assay (ELISA) and enzyme labeling were used to determine the expression levels of NF-κB P65, IL-6, and NO in the subjects. [6] aureus strains in Western blotting and double antibody sandwich ELISA. [7] The results indicated that the diagnostic specificity and sensitivity of the LFI strip test were greater than the double antibody sandwich (DAS) DAS ELISA. [8] Collected samples were analyzed by Double Antibody Sandwich Enzyme Linked Immunosorbent Assay (DAS–ELISA) for detection CPMMV. [9] We screened 76,530 healthy blood donors for hepatitis B virus (HBV) visiting Mayo Hospital, Lahore, Pakistan during 2016 and 2017 with rapid test kits which used lateral flow immunoassay based on the principle of double antibody sandwich technique. [10] Leaf samples from 2090 trees showing and not showing virus-like symptoms were tested by double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) for PDV infection. [11] Conclusion The established double antibody sandwich ELISA has good accuracy, precision, and specificity, and can be used for rapid detection of AdC68 protein contents in AdC68 purification process. [12] The sensitivity of double antibody sandwich Gh-TRFIA was 0. [13] Collected samples were analyzed by Double Antibody Sandwich Enzyme Linked Immunosorbent Assay (DAS–ELISA) for detection CPMMV. [14] Proper expression in maize and immunoreactivity of the chimeric protein (PD-FcIgY) to chicken anti- IBDV and anti-rVP2 Ab were confirmed by both direct and indirect double antibody sandwich (DAS)-ELISAs as well as western blotting. [15] A total of 29 symptomatic plants were collected and tested using double antibody sandwich (DAS)-ELISA kits (DSMZ, Braunschweig, Germany) for the presence of OYDV and LYSV and a triple antibody sandwich ELISA kit (DSMZ) for shallot latent virus (SLV). [16] The Bone Glaprotein (BGP), hematocrit (Hct), alkaline phosphatase (ALP), matrix metalloproteinase-3 (MMP-3), CRP and TNF-α were detected by double antibody sandwich enzyme-linked immunosorbent assay. [17] The levels of IgG subclasses in blood plasma were detected by double antibody sandwich ELISA in healthy persons and AIHA patients, at the same time. [18] Serum midkine level was assessed by double antibody sandwich assay technique(ELISA) by using human midkine ELISA kit also CA 15-3 level was assessed by using an automatic immune assay analyzer (TOSOH AIA system). [19] In this work, the lateral flow immunoassay (LFIA) based on double antibody sandwich technique is developed using bright fluorescent cadmium telluride quantum dots (CdTe QDs). [20] Human PTX3 concentration was measured with a commercially available ELISA kit, using a double antibody sandwich enzyme-linked immunosorbent assay. [21] Samples were tested for MLN causing viruses by Double Antibody Sandwich Enzyme-Linked Immunosorbent Assay (DAS-ELISA) and Reverse Transcriptase-Polymerase Chain Reaction (RT-PCR). [22] The serum levels of TSH, Lp-PLA2, TNF-α and IL-6 were measured by up-converting phoshor assay and enzyme - linked immunosorbent assay with double antibody sandwich. [23] Here, we demonstrated that SCMV strain FZ1 can systemically infect Brachypodium distachyon inbred line Bd21 and Nicotiana benthamiana through inoculation, double antibody sandwich enzyme-linked immunosorbent, transmission electron microscopy, and reverse transcription PCR assays. [24] To achieve this, we studied and designed a giant magneto resistance (GMR) multi-biomarker immunoassay biosensor that can simultaneously detect twelve kinds of tumor markers by integrating a GMR sensor chip, a microfluidic device, a magnetic nano-beads label, and a double antibody sandwich immunoassay method. [25] Testing the collected samples for the presence of turnip mosaic virus (TuMV) by double antibody sandwich-enzyme linked immunosorbent assay (DAS-ELISA) and reverse transcription-polymerase chain reaction (RT-PCR) confirmed that 117 samples were infected with TuMV. [26] Methods A total of 5 787 fecal samples from children under 10 years old in four hospitals in Xiamen from Jan 2016 to Dec 2017 were detected by immunochromamatoraphy double antibody sandwich assay. [27] BYDV-PAV ve BYDV-MAV’in varligi DAS-ELISA (Double antibody sandwich enzyme linked immunosorbent assay) test yontemi ile belirlenmistir. [28] In this paper, a series of Songorine derivatives were synthesized and their inhibitory activities on GPCRs were also evaluated by using the Double Antibody Sandwich ELISA (DAS-ELISA) in vitro. [29] Double antibody sandwich enzyme-linked immunosorbent assay (ELISA) was used to determine the expression levels of IL-10 and G-CSF in serum before and after treatment. [30] Seven pumpkin plants with typical mosaic symptoms were tested by double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) using antibodies for cucumber mosaic virus (Agdia, Elkhart, IN) and squash mosaic virus (Agdia), respectively. [31] The expression of IL-6, IL-10, IL-17, NSE and S100β in peripheral blood of children in each group were detected by double antibody sandwich enzyme-linked immunosorbent assay (ELISA). [32] The level of NLRP3 in peripheral blood was analyzed by ELISA double antibody sandwich method. [33] Obtained antibodies were evaluated using Double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA), and Immune Dot-Blot assay. [34] The presence of CatMV in collected samples was tested by double antibody sandwich enzyme linked immunosorbent assay and was confirmed by reverse transcription polymerase chain reaction using specific primers. [35] The serum levels of serum creatinine( SCr),urea nitrogen( BUN),plasma endotoxin level,24 h urinary protein and D-lactate in the plasma were determined by sarcosine oxidase,urease method,tal reagent method,bromo cresol chloroform method and double antibody sandwich enzyme-linked immunoadsorbent assay,respectively. [36] A sensitive and specific enzyme-linked immunosorbent assay (ELISA) for the detection of Somatostatin based on double antibody sandwich method was studied in this paper. [37] The serum Klotho levels of CKD patients and control group at different stages were detected by double antibody sandwich ELISA, and the differences between each group were compared. [38] Samples were analysed in Laboratory of Rwanda Agriculture Board, using Double Antibody Sandwich Enzyme Linked Immuno Sorbent Assay. [39] The serum IMA level was detected by double antibody sandwich enzyme-linked immunosorbent assay (ELISA), and the plasma D-D level was detected by immunoturbidimetry. [40] Toplanan ornekler double antibody sandwich enzyme-linked immunosorbent assay (DAS-ELISA) yontemi ile TuMV’nin varliginin belirlenmesi amaci ile testlenmistir. [41] The levels of IL-10 and TNF-α in the collected samples that EPS were determined by double antibody sandwich ELISA. [42] The level of 5-hydroxytryptamine (5-HT) was measured by double antibody sandwich method. [43] ABSTRACT In this study, we developed a double antibody sandwich chemiluminescent immunoassay (DAS-CLIA) based on phage-displayed nanobodies for the determination of Cry2A toxin. [44] The quality of life was assessed by SF-36 Health Survey (SF-36) before and after treatment, serum Ca, P and ALP levels were measured by colorimetry, and intact parathyroid hormone (iPTH) was detected by double antibody sandwich ELISA. [45] The Scr was detected by deproteinized alkaline picric acid method, and BUN was detected by rate method, and serum albumin (ALb) was detected by bromocresol green dye binding method, and 24 hours urinary protein was measured by pyrogallol red colorimetry, and the double antibody sandwich ELISA method was used for detection of urinary C5b-9. [46] In the present study a double antibody sandwich ELISA exploring, monoclonal antibodies and hyperimmune serum, raised against recombinant variable surface glycoprotein has been developed to detect circulating trypanosome antigens. [47] The assay was based on double antibody sandwich format with the visual detection limit (vLOD) of 0. [48] Subsequently, the serum fibroblast growth factor-23 levels were measured by double antibody sandwich ABC-ELISA, and the relationship between vascular calcification score and fibroblast growth factor-23 level was analyzed by Spearman method. [49] Here, three triple bonds (C≡N and C≡C) coded SERS tags contribute separate SERS emissions located at 2105, 2159, and 2227 cm-1, respectively; must have one-to-one correspondence from AFP, to FER, to CEA, In the process of detection, the mature double antibody sandwich allows the formation of microscale core-satellite assembly structure between a magnetic bead (MB) and single SERS tags, and therefore a pure and single SERS emission can be observed under the routine excitation laser spot. [50]실험군 소아의 BALF에서 MCP-4, IL-25, TNF-α 및 CysLTR-1의 수준은 이중항체 샌드위치 ELISA로 측정하였다. [1] 이 연구에서는 이중 항체 샌드위치 방법과 결합된 표면 강화 라만 산란(SERS) 검출 플랫폼을 사용하여 PROM 환자의 혈청에서 PCT를 정량적으로 검출했습니다. [2] 9개의 샬롯 밭에서 총 18개의 증상 식물을 수집하여 SVX용 이중 항체 샌드위치 ELISA 키트(DSMZ RT-1042) 및 TAS-ELISA 키트(DSMZ RT-0514-0512/1)로 SLV를 테스트했습니다. [3] nan [4] 이중 항체 샌드위치 방법을 기반으로 한 C-펩티드 검출을 위한 민감하고 특이적인 이중 항체 샌드위치 효소 결합 면역흡착 분석법이 본 논문에서 연구되었습니다. [5] 면역 조직 화학, 이중 항체 샌드위치 효소 결합 면역 흡착 분석(ELISA) 및 효소 표지를 사용하여 대상체에서 NF-κB P65, IL-6 및 NO의 발현 수준을 결정했습니다. [6] 웨스턴 블롯팅 및 이중 항체 샌드위치 ELISA에서 aureus 균주. [7] 그 결과 LFI 스트립 검사의 진단 특이도와 민감도가 DAS(Double Antibody Sandwich) DAS ELISA보다 높았다. [8] 수집된 샘플을 CPMMV 검출을 위해 DAS-ELISA(Double Antibody Sandwich Enzyme Linked Immunosorbent Assay)로 분석했습니다. [9] 2016년과 2017년 파키스탄 라호르의 Mayo Hospital을 방문한 건강한 B형 간염 바이러스(HBV) 헌혈자 76,530명을 대상으로 이중항체 샌드위치 기법의 원리를 기반으로 하는 측방유동 면역분석법을 이용한 신속진단키트를 이용했습니다. [10] nan [11] nan [12] 이중항체 샌드위치 Gh-TRFIA의 민감도는 0이었다. [13] nan [14] nan [15] 총 29개의 증상 식물을 수집하여 OYDV 및 LYSV의 존재에 대한 이중 항체 샌드위치(DAS)-ELISA 키트(DSMZ, Braunschweig, Germany)와 샬롯 잠복 바이러스(SLV)에 대한 삼중 항체 샌드위치 ELISA 키트(DSMZ)를 사용하여 테스트했습니다. ). [16] nan [17] 건강한 사람과 AIHA 환자에서 동시에 이중 항체 샌드위치 ELISA에 의해 혈장 내 IgG 하위 클래스의 수준이 검출되었습니다. [18] 혈청 미드카인 수준은 인간 미드카인 ELISA 키트를 사용하여 이중 항체 샌드위치 분석 기법(ELISA)에 의해 평가되었고 CA 15-3 수준은 자동 면역 분석 분석기(TOSOH AIA 시스템)를 사용하여 평가되었습니다. [19] 이 작업에서 이중 항체 샌드위치 기술을 기반으로 하는 측면 유동 면역 분석(LFIA)은 밝은 형광 카드뮴 텔루르화물 양자점(CdTe QD)을 사용하여 개발되었습니다. [20] nan [21] nan [22] TSH, Lp-PLA2, TNF-α 및 IL-6의 혈청 수준은 이중 항체 샌드위치를 사용한 상향 변환 인광 분석 및 효소 결합 면역흡착 분석에 의해 측정되었습니다. [23] nan [24] 이를 위해 우리는 GMR 센서 칩, 미세유체 소자, 자기 나노비드 라벨 및 이중 구조를 통합하여 12가지 종류의 종양 표지자를 동시에 검출할 수 있는 거대 자기저항(GMR) 다중 바이오마커 면역분석 바이오센서를 연구 및 설계했습니다. 항체 샌드위치 면역분석법. [25] nan [26] nan [27] nan [28] 본 논문에서는 DAS-ELISA(Double Antibody Sandwich ELISA)를 사용하여 in vitro에서 일련의 Songorine 유도체를 합성하고 GPCR에 대한 억제 활성을 평가했습니다. [29] nan [30] nan [31] nan [32] nan [33] nan [34] nan [35] nan [36] nan [37] 이중항체 샌드위치 ELISA를 통해 만성콩팥병 환자와 대조군의 혈청 Klotho 농도를 병기별로 검출하여 각 군 간의 차이를 비교하였다. [38] nan [39] nan [40] nan [41] EPS가 수집된 샘플에서 IL-10 및 TNF-α의 수준은 이중 항체 샌드위치 ELISA에 의해 결정되었습니다. [42] 5-히드록시트립타민(5-HT)의 수준은 이중 항체 샌드위치 방법으로 측정하였다. [43] 초록 이 연구에서 우리는 Cry2A 독소 측정을 위해 파지 표시 나노바디를 기반으로 하는 이중 항체 샌드위치 화학발광 면역분석법(DAS-CLIA)을 개발했습니다. [44] 삶의 질은 치료 전후에 SF-36 Health Survey(SF-36)에 의해 평가되었고, 혈청 Ca, P 및 ALP 수치는 비색법으로, 온전한 부갑상선 호르몬(iPTH)은 이중항체 샌드위치 ELISA로 검출되었습니다. [45] Scr은 탈단백 알칼리성 피크르산법으로, BUN은 rate법으로, 혈청 알부민(ALb)은 bromocresol green dye binding법으로, 24시간 요단백은 pyrogallol red colorimetry로, 이중항체는 샌드위치 ELISA 방법은 소변 C5b-9의 검출을 위해 사용되었습니다. [46] 현재 연구에서 이중 항체 샌드위치 ELISA 탐색, 재조합 가변 표면 당단백질에 대해 제기된 단일클론 항체 및 과면역 혈청이 순환하는 트리파노솜 항원을 검출하기 위해 개발되었습니다. [47] 분석은 시각적 검출 한계(vLOD)가 0인 이중 항체 샌드위치 형식을 기반으로 했습니다. [48] 이어서, 혈청 섬유아세포 성장인자-23 수치를 이중항체 샌드위치 ABC-ELISA로 측정하였고, 혈관 석회화 점수와 섬유아세포 성장인자-23 수치의 관계를 Spearman 방법으로 분석하였다. [49] nan [50]