Littérature scientifique sur le sujet « Nano-Antibody »
Créez une référence correcte selon les styles APA, MLA, Chicago, Harvard et plusieurs autres
Consultez les listes thématiques d’articles de revues, de livres, de thèses, de rapports de conférences et d’autres sources académiques sur le sujet « Nano-Antibody ».
À côté de chaque source dans la liste de références il y a un bouton « Ajouter à la bibliographie ». Cliquez sur ce bouton, et nous générerons automatiquement la référence bibliographique pour la source choisie selon votre style de citation préféré : APA, MLA, Harvard, Vancouver, Chicago, etc.
Vous pouvez aussi télécharger le texte intégral de la publication scolaire au format pdf et consulter son résumé en ligne lorsque ces informations sont inclues dans les métadonnées.
Articles de revues sur le sujet "Nano-Antibody"
Peng, Jianyun, Yongling Tao, Xiaoru Zhang, Meijuan Xiang, Zhihong Gui, Jing Wu et Liqing Yin. « Effect of Preparation of β2M Nano Antibody Adsorbent for Blood Purification on Dialysis Complications in Patients with Renal Failure ». Science of Advanced Materials 13, no 1 (1 janvier 2021) : 161–70. http://dx.doi.org/10.1166/sam.2021.3881.
Texte intégralWang, Yi, Yujin Feng, Xiaoyun Yang, Wengang Wang et Yueheng Wang. « Diagnosis of Atherosclerotic Plaques Using Vascular Endothelial Growth Factor Receptor-2 Targeting Antibody Nano-microbubble as Ultrasound Contrast Agent ». Computational and Mathematical Methods in Medicine 2022 (5 mai 2022) : 1–7. http://dx.doi.org/10.1155/2022/6524592.
Texte intégralMahmoudi, Tohid, Mohammad Pourhassan-Moghaddam, Behnaz Shirdel, Behzad Baradaran, Eden Morales-Narváez et Hamed Golmohammadi. « (Nano)tag–antibody conjugates in rapid tests ». Journal of Materials Chemistry B 9, no 27 (2021) : 5414–38. http://dx.doi.org/10.1039/d1tb00571e.
Texte intégralGupta, Ankur, Monalisha Nayak, Deepak Singh et Shantanu Bhattacharya. « Antibody immobilization for ZnO nanowire based biosensor application ». MRS Proceedings 1675 (2014) : 33–39. http://dx.doi.org/10.1557/opl.2014.848.
Texte intégralSouto, Elizabeth XISTO, Laiz CAMEIRAO Bento, Flavia ARANDAS Sousa, Marilia SANDOVAL Passaro, Andressa DA COSTA Vaz, Daniela Schimidell, Barbara FAZIALI Bueno et al. « Anti-CD38 Nanoantibody (JK36) Allows Detection of Minimal Residual Disease in Multiple Myeloma Patients Treated with Daratumumab ». Blood 142, Supplement 1 (28 novembre 2023) : 4703. http://dx.doi.org/10.1182/blood-2023-182757.
Texte intégralPuertas, S., M. Moros, R. Fernández-Pacheco, M. R. Ibarra, V. Grazú et J. M. de la Fuente. « Designing novel nano-immunoassays : antibody orientation versus sensitivity ». Journal of Physics D : Applied Physics 43, no 47 (11 novembre 2010) : 474012. http://dx.doi.org/10.1088/0022-3727/43/47/474012.
Texte intégralKumar D. R, Santhosh, et Dr P.V. Rao. « HPV Sensing by CNTFET Array Nanobiosensor. » International Journal of Engineering & ; Technology 7, no 3.34 (1 septembre 2018) : 82. http://dx.doi.org/10.14419/ijet.v7i3.34.18778.
Texte intégralCao, Fei, Qian Yao, Tieshan Yang, Zhao Zhang, Yu Han, Jinchao Feng et Xiu-Hong Wang. « Marriage of antibody–drug conjugate with gold nanorods to achieve multi-modal ablation of breast cancer cells and enhanced photoacoustic performance ». RSC Advances 6, no 52 (2016) : 46594–606. http://dx.doi.org/10.1039/c6ra01557c.
Texte intégralSchneider, Constantin, Matthew I. J. Raybould et Charlotte M. Deane. « SAbDab in the age of biotherapeutics : updates including SAbDab-nano, the nanobody structure tracker ». Nucleic Acids Research 50, no D1 (19 novembre 2021) : D1368—D1372. http://dx.doi.org/10.1093/nar/gkab1050.
Texte intégralBuyukserin, Fatih, Colin D. Medley, Miguel O. Mota, Kaan Kececi, Richard R. Rogers, Weihong Tan et Charles R. Martin. « Antibody-functionalized nano test tubes target breast cancer cells ». Nanomedicine 3, no 3 (juin 2008) : 283–92. http://dx.doi.org/10.2217/17435889.3.3.283.
Texte intégralThèses sur le sujet "Nano-Antibody"
Hmaidi, Riadh. « Nouvelle stratégie basée sur les polypeptides comme agents modulateurs des processus tumoraux ». Electronic Thesis or Diss., Amiens, 2022. http://www.theses.fr/2022AMIE0073.
Texte intégralNatural molecules are increasingly being researched and tested for their therapeutic potential. Scorpion venoms derived peptides modulating ion channels activity are robust biological essential tools for a better understanding of the action mechanisms of these transmembrane channels, particularly sodium channels. They represent sometimes the major molecules of the venom responsible for its highly toxic effect which manifests with cardiogenic syndromes and pulmonary edema often fatal for humans. By modulating ion channels activity, these molecules are potentially able to act on the cellular processes associated with them. In the first part of this work, we have studied the mechanism of interaction of the AahII toxin from the scorpion venom of Androctonus australis hector (Aah), with the voltage-gated sodium channel NaV1.5 and its effect on the electrophysiological activity of this channel. In particular, we studied the ability of the anti-AahII nanoantibody (NbAahII 10 or Nb10) to neutralize the AahII/NaV1.5 interactions. In the second part, we investigated the effect of different peptide fractions from Aah venom on the viability of human breast cancer cells. The toxin AahII is the most active α-toxin from the North African scorpion Androctonus australis hector that slows the fast inactivation of NaV channels. To fight scorpion envenomation, an anti-AahII nanobody named NbAahII10 (Nb10) was developed. The efficiency of this nanobody has been evaluated in vivo on mice, but its mechanism of action at the cellular level remains unknown. Our work confirmed that the AahII toxin slows the fast inactivation of the adult cardiac NaV1.5 channels, expressed in HEK293 cells, in a dose-dependent manner, while current amplitude was not affected, and showed that Nb10 can fully reverse the effect of the AahII toxin on the channel inactivation kinetics. Bioinformatic analysis of the NaV1.5/AahII interaction complex shows that AahII shares the same interaction surface with Nb10, which strongly suggests that Nb10 dynamically replaces the AahII toxin from its binding site on the NaV1.5 channel. At the pathophysiological level, we showed that treatment of human breast cancer cells MDA-MB-231 with Nb10 prevents the increase in cell invasion induced by AahII. In the second part of this work, the 3 major fractions from Aah scorpion venom, previously isolated by low-pressure chromatography (M1, M2, and AahG50), were tested on the viability and migration of human breast cancer cell lines, MCF-7 and MDA-MB-231. These fractions did not affect cell migration but induced very biphasic effects on cell viability, interestingly demonstrating synergistic or antagonistic effects of their component peptides. To purify the peptides of interest, additional purification of the fractions was performed by high-pressure chromatography (HPLC). In total, three polypeptides were identified to induce a decrease in breast cancer cell viability and will be further investigated. In conclusion, our results elucidated the physiological and molecular mechanisms of α-toxin AahII neutralization by the Nb10 nanoantibody. In addition, we were able to identify three peptide molecules from the scorpion venom Aah with anticancer properties. This work will continue with a structural study to elucidate the underlying molecular topologies at a three-dimensional scale
SIRONI, LAURA. « Nanoparticles for in-vitro and in-vivo biosensing and imaging ». Doctoral thesis, Università degli Studi di Milano-Bicocca, 2011. http://hdl.handle.net/10281/19278.
Texte intégralDréan, Raphaelle. « Développement de nano-anticorps antagonistes du point de contrôle immunitaire ILT4 pour une application en immunothérapie antitumorale ». Electronic Thesis or Diss., Sorbonne université, 2022. http://www.theses.fr/2022SORUS446.
Texte intégralILT4 (Immunoglobulin-Like Transcript 4) is an immune checkpoint receptor mainly expressed by myeloid immune cells. In cancer context, ILT4 participates in tumor development by maintaining a protumoral immuno-microenvironment and directly promoting tumor cell proliferation. ILT4 interaction with the non-classical MCH class I molecule HLA-G induces an immunosuppressive microenvironment by promoting tolerogenic myeloid cells. Moreover, the ectopic expression of ILT4 has been reported in several solid tumors. The activation of ILT4 by Angiopoietin-like-2 (ANGPTL2) promotes non-small cell lung tumor cell proliferation and inhibits cell apoptosis. Targeting this new immune checkpoint with blocking antibodies is therefore a promising cancer immunotherapy approach. In light of several drawbacks of classical IgG blocking antibodies in solid cancer, we investigated the potential of VHH-based inhibitors. This small monoclonal antibody format, derived from camelid homodimeric antibodies, combine the binding capacities of antibodies to the properties of small molecules. After immunization of an alpaca and phage-display screening, we selected a VHH with high affinity and specificity to ILT4 that inhibits the interaction of the receptor with both ligands. We validated the VHH’s biological antagonist activity on tumor cells and monocyte-derived pro-tumoral M2 like macrophages in vitro. These results support the potential of this new VHH-based antibody targeting ILT4 in cancer immunotherapy
Chen, Chiao-Yu, et 陳喬郁. « Isolation of monoclonal antibody with binding activity specific to bio-nano interface ». Thesis, 2015. http://ndltd.ncl.edu.tw/handle/829k33.
Texte intégral國立交通大學
材料科學與工程學系奈米科技碩博士班
104
There are more and more application of nano-materials in medicine and biotechnology. The interest in nano-systems for biological applications is continuously growing. To explore the potential of nano-material in the application of drug delivery, artificial implants, and bio-electronics, the fundamental rules underlining the bio-nano interaction should be carefully investigated. Understanding the bio-nano interface is the key to develop and better use of bionanotechnology. I have demonstrated several specific bio-nano interface previously. I also showed that antibody can recognize gold nanoparticles. Our approach is to develop monoclonal antibody against gold nanoparticles which will serve as the base for further biophysical study and applications. The result indicated that I was able to isolate monoclonal antibody that still maintained the specific binding activity. The single-molecule electrical conductance of the protein transistor made by this antibody revealed the dynamic binding which confirmed the thermodynamics of the binding. Production of monoclonal antibodies consists of four steps: immunizing the animal usually a mouse, obtaining immune cells from the spleen of the immunized mouse, fusing the spleen cells with myeloma cells to obtain hybridomas, and selecting the hybridoma cell line producing the desired monoclonal antibody. I immunized mice using gold nanoparticles. The spleens of positive mice were fused with melanoma. The successful fusion cells were properly dilute and monoclonal antibody was produced. To monitor the binding activity, a special ELISA was designed to distinguish the binding activities of this bio-nano interaction. For example, I was able to assay for different interactions such as the IgG-gold surface, IgG-physical size, and IgG-shape. In addition, the bio-nano interaction was detected by the single-molecule electrical conductance platform, for a final confirmation.
Balakrishnan, Arjun. « Unravelling the Mechanism of Bactericidal/Permeability-Increasing Protein Expression during Bacterial Pathogenesis ». Thesis, 2016. http://etd.iisc.ac.in/handle/2005/3155.
Texte intégralBalakrishnan, Arjun. « Unravelling the Mechanism of Bactericidal/Permeability-Increasing Protein Expression during Bacterial Pathogenesis ». Thesis, 2016. http://hdl.handle.net/2005/3155.
Texte intégralChapitres de livres sur le sujet "Nano-Antibody"
Chen, Yeong-Renn. « EPR Spin-Trapping and Nano LC MS/MS Techniques for DEPMPO/•OOH and Immunospin-Trapping with Anti-DMPO Antibody in Mitochondrial Electron Transfer System ». Dans Methods In Molecular Biology, 75–88. Totowa, NJ : Humana Press, 2008. http://dx.doi.org/10.1007/978-1-60327-517-0_7.
Texte intégralIgnatov, Sergei Georgievich, S. Yu Filippovich et Ivan Alekseevich Dyatlov. « Specific Immobilization of Rotaviruses for Atomic Force Microscopy Using Langmuir Antibody Films Based on Amphiphilic Polyelectrolytes ». Dans Macro, Micro, and Nano-Biosensors, 117–31. Cham : Springer International Publishing, 2021. http://dx.doi.org/10.1007/978-3-030-55490-3_7.
Texte intégralMokhtari, Wafaa, Mohamed Achouri, Abdellah Remah, Noureddine Chtaina et Hassan Boubaker. « Nano-Biosensors Tech and IPM in Plant Protection to Respond to Climate Change Challenges in Morocco ». Dans Sensor Network Methodologies for Smart Applications, 114–29. IGI Global, 2020. http://dx.doi.org/10.4018/978-1-7998-4381-8.ch005.
Texte intégralBhattacharya, Sankha, et Kapil Gore. « Targeted Cancer Therapy Using Nanoparticles and Antibody Fragments ». Dans Advances in Precision Medicine Oncology. IntechOpen, 2021. http://dx.doi.org/10.5772/intechopen.96550.
Texte intégralMukherjee, D. « ZnO for Probes in Diagnostics ». Dans ZnO and Their Hybrid Nano-Structures, 202–33. Materials Research Forum LLC, 2023. http://dx.doi.org/10.21741/9781644902394-7.
Texte intégralActes de conférences sur le sujet "Nano-Antibody"
Ding, Ann-Ann, Ying-Yi Chen, Churng-Ren Chris Wang, Pai-Chi Li et Dar-Bin Shieh. « HER-2 Antibody Conjugated Gold Nano Rod for in Vivo Photothermal Therapy ». Dans 2008 8th IEEE Conference on Nanotechnology (NANO). IEEE, 2008. http://dx.doi.org/10.1109/nano.2008.264.
Texte intégralIshijima, Ayumu, Shinya Yamahira, Satoshi Yamaguchi, Etsuko Kobayashi, Yoshikazu Shibasaki, Takashi Azuma, Teruyuki Nagamune et Ichiro Sakuma. « Notice of Removal : Antibody-conjugated phase-change nano-droplet for ultrasound therapeutic agent ». Dans 2017 IEEE International Ultrasonics Symposium (IUS). IEEE, 2017. http://dx.doi.org/10.1109/ultsym.2017.8092636.
Texte intégralUda, M. N. A., C. M. Hasfalina, A. A. Samsuzanaa, S. Faridah, I. Zamri, B. Siti Noraini, W. Nur Sabrina, U. Hashim et Subash C. B. Gopinath. « Immunosensor development formatting for tungro disease detection using nano-gold antibody particles application ». Dans 11TH ASIAN CONFERENCE ON CHEMICAL SENSORS : (ACCS2015). Author(s), 2017. http://dx.doi.org/10.1063/1.4975290.
Texte intégralSha, Jingjie, Fangzhou Fu, Bing Xu, Ke Chen et Xiao Li. « Evaluation of the Binding of PD-1 Antibody and Antigen Using Nano-Sensors ». Dans 2019 20th International Conference on Solid-State Sensors, Actuators and Microsystems & Eurosensors XXXIII (TRANSDUCERS & EUROSENSORS XXXIII). IEEE, 2019. http://dx.doi.org/10.1109/transducers.2019.8808675.
Texte intégralChoi, Eunpyo, Yuri Choi et Jungyul Park. « Specific and label-free immunoglobulin G antibody detection using nano porous hydrogel photonic crystals ». Dans TRANSDUCERS 2011 - 2011 16th International Solid-State Sensors, Actuators and Microsystems Conference. IEEE, 2011. http://dx.doi.org/10.1109/transducers.2011.5969328.
Texte intégralUda, M. N. A., C. M. Hasfalina, A. A. Samsuzana, U. Hashim, Shahrul A. B. Ariffin, Zamri I., Nur Sabrina W. et al. « Immunosensor development for rice tungro bacilliform virus (RTBV) detection using antibody nano-gold conjugate ». Dans 11TH ASIAN CONFERENCE ON CHEMICAL SENSORS : (ACCS2015). Author(s), 2017. http://dx.doi.org/10.1063/1.4975291.
Texte intégralOHUCHI, NORIAKI, MORIO NAKAJIMA, HIROSHI TADA, TAKANORI ISHIDA, MOTOHIRO TAKEDA et HIDEO HIGUCHI. « NANO-SENSING CAPSULES FOR MEDICAL APPLICATION : NANO-PARTICLES FOR SENTINEL NAVIGATION AND QUANTUM DOTS CONJUGATION WITH ANTI-HER2 ANTIBODY FOR MOLECULAR IMAGING OF CANCER ». Dans Proceedings of the Final Symposium of the Tohoku University 21st Century Center of Excellence Program. IMPERIAL COLLEGE PRESS, 2006. http://dx.doi.org/10.1142/9781860948800_0027.
Texte intégralTseng, Shin-Hua, Dion T. Tseng, Tzu-Cheng Lee, Tsai-Mu Cheng, Jyh-Yuan Yang, Ruo-Yu Hsieh, Chuan-Mei Tsai et Chia-Ching Chang. « Ultra Sensitive Detection of Eneterovirus 71 by Modified Electrochemical Impedance Spectroscopy ». Dans ASME 2010 First Global Congress on NanoEngineering for Medicine and Biology. ASMEDC, 2010. http://dx.doi.org/10.1115/nemb2010-13143.
Texte intégralMallakin, Ali, Kazushi Inoue et Martin Guthold. « In-Situ Quantitative Analysis of Tumor Suppressor Protein (hDMP1) Using a Nanomechanical Cantilever Beam ». Dans ASME 2005 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. ASMEDC, 2005. http://dx.doi.org/10.1115/detc2005-84503.
Texte intégralWang, Wei-Jhen, Chia-Hwa Lee, Chin-Wen Li, Stephen Liao, Fuh-Jyh Jan et Gou-Jen Wang. « Direct Label Free Detection of Orchid Virus Using a Micro/Nano Hybrid Structured Biosensor ». Dans ASME 2019 International Design Engineering Technical Conferences and Computers and Information in Engineering Conference. American Society of Mechanical Engineers, 2019. http://dx.doi.org/10.1115/detc2019-97198.
Texte intégral