Relevant bibliographies by topics / Tandem-affinity purification

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Tandem-affinity purification'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 April 2022

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Journal articles on the topic "Tandem-affinity purification"

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Soleimani, Vahab D., Gareth A. Palidwor, Parameswaran Ramachandran, Theodore J. Perkins, and Michael A. Rudnicki. "Chromatin tandem affinity purification sequencing." Nature Protocols 8, no. 8 (2013): 1525–34. http://dx.doi.org/10.1038/nprot.2013.088.

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Maine, G. N., N. Gluck, I. W. Zaidi, and E. Burstein. "Bimolecular Affinity Purification (BAP): Tandem Affinity Purification Using Two Protein Baits." Cold Spring Harbor Protocols 2009, no. 11 (2009): pdb.prot5318. http://dx.doi.org/10.1101/pdb.prot5318.

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Amberg, David C., Daniel J. Burke, and Jeffrey N. Strathern. "Tandem Affinity Protein (TAP) Purification from Yeast." Cold Spring Harbor Protocols 2006, no. 1 (2006): pdb.prot4153. http://dx.doi.org/10.1101/pdb.prot4153.

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Li, Yifeng. "The tandem affinity purification technology: an overview." Biotechnology Letters 33, no. 8 (2011): 1487–99. http://dx.doi.org/10.1007/s10529-011-0592-x.

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Van Leene, Jelle, Erwin Witters, Dirk Inzé, and Geert De Jaeger. "Boosting tandem affinity purification of plant protein complexes." Trends in Plant Science 13, no. 10 (2008): 517–20. http://dx.doi.org/10.1016/j.tplants.2008.08.002.

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Li, Yifeng. "Commonly used tag combinations for tandem affinity purification." Biotechnology and Applied Biochemistry 55, no. 2 (2010): 73–83. http://dx.doi.org/10.1042/ba20090273.

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Mishra, Vibhor. "Affinity Tags for Protein Purification." Current Protein & Peptide Science 21, no. 8 (2020): 821–30. http://dx.doi.org/10.2174/1389203721666200606220109.

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The affinity tags are unique proteins/peptides that are attached at the N- or C-terminus of the recombinant proteins. These tags help in protein purification. Additionally, some affinity tags also serve a dual purpose as solubility enhancers for challenging protein targets. By applying a combinatorial approach, carefully chosen affinity tags designed in tandem have proven to be very successful in the purification of single proteins or multi-protein complexes. In this mini-review, the key features of the most commonly used affinity tags are discussed. The affinity tags have been classified into
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GOULD, K. "Tandem affinity purification and identification of protein complex components." Methods 33, no. 3 (2004): 239–44. http://dx.doi.org/10.1016/j.ymeth.2003.11.019.

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Stingl, Kerstin, Kristine Schauer, Chantal Ecobichon, et al. "In VivoInteractome ofHelicobacter pyloriUrease Revealed by Tandem Affinity Purification." Molecular & Cellular Proteomics 7, no. 12 (2008): 2429–41. http://dx.doi.org/10.1074/mcp.m800160-mcp200.

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Kaneko, Aki, Takashi Umeyama, Nozomu Hanaoka, Brian C. Monk, Yoshimasa Uehara, and Masakazu Niimi. "Tandem affinity purification of theCandida albicans septin protein complex." Yeast 21, no. 12 (2004): 1025–33. http://dx.doi.org/10.1002/yea.1147.

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Dissertations / Theses on the topic "Tandem-affinity purification"

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Zhang, Shuang. "Tandem Affinity Purification of Myogenin and Characterization of the Tcap Promoter." OpenSIUC, 2010. https://opensiuc.lib.siu.edu/theses/205.

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Myogenesis is orchestrated by a family of four related bHLH transcription factors; MyoD, Myf5, Myogenin and Mrf4. The MRFs form heterodimers with E proteins and bind to the promoters or enhancers of muscle specific genes. Of these four, the Myogenic Regulatory Factor (MRF), myogenin, has been shown to play an important role during terminal differentiation of skeletal muscle. However, little is known about myogenin's function during myogenesis. In order to reveal myogenin associated factors, we performed tandem affinity purification of myogenin. The TAP purification with HEK293 cells elucidate
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Holzberg, David Alexander. "Untersuchungen zur spezifischen Funktion von JNK-Signalwegen mit Hilfe von zellpermeablen Peptiden und tandem affinity purification." [S.l. : s.n.], 2004. http://deposit.ddb.de/cgi-bin/dokserv?idn=972264175.

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Davidora, Albena. "Validation and characterization of putative NHE6-interacting proteins identified by yeast two-hybrid screening and tandem affinity purification :." Thesis, McGill University, 2007. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=100793.

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Na+/H+ exchangers (NHE) are integral membrane proteins that catalyze the electroneutral exchange of Na+ (or K+) for H+. The nine human isoforms identified to date share the same topology of twelve membrane-spanning domains and a cytoplasmic regulatory tail, and diverge in their tissue expressions and subcellular localizations. This thesis focused on the identification and characterization of proteins interacting with the ubiquitous NHE6 isoform, which resides predominantly in recycling endosomes. Recent yeast two-hybrid (Y2H) screening of a human brain cDNA library using the regulatory tail of
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Pek, Denis [Verfasser]. "Identifizierung von K-Ras-Interaktionspartnern in der humanen Pankreaskarzinomzelllinie PANC-1 mittels des tandem affinity purification-Systems / Denis Pek." Ulm : Universität Ulm. Medizinische Fakultät, 2014. http://d-nb.info/1052935869/34.

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Moreno, Iglesias Ana. "Caracterización de la MAP kinasa ERK5 en células neuronales: papel en la isquemia cerebral e identificación de proteínas asociadas mediante tandem affinity purification." Doctoral thesis, Universitat Autònoma de Barcelona, 2009. http://hdl.handle.net/10803/3599.

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La vía de señalización celular MEK5-ERK5 juega un papel importante en sistema nervioso, dado que se activa frente a neurotrofinas, frente al estrés oxidativo producido por reactive oxygen species (ROS), tras la isquemia cerebral y tiene un papel en la especificación de fenotipo neuronal. Sin embargo, poco se conoce sobre los sustratos y proteínas que interaccionan con ERK5. En este trabajo se han identificado proteínas que interaccionan con ERK5 en células de neuroblastoma SH-SY5Y mediante el método TAP (Tandem-Affinity Purification). Se han obtenido diversas proteínas que incluyen proteínas d
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Zhao, Hongwei. "A Proteomic Study of Plant Messenger RNA Cleavage and Polyadenylation Specificity Factors and the Establishment of an In Vitro Cleavage Assay System." Oxford, Ohio : Miami University, 2008. http://rave.ohiolink.edu/etdc/view?acc%5Fnum=miami1218547019.

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Desai, Shruti. "Regulation of Positive Regulatory Domain I- Binding Factor 1 and Its Role in Mantle Cell Lymphoma." Scholar Commons, 2010. https://scholarcommons.usf.edu/etd/1613.

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The human positive regulatory domain I binding factor 1 (PRDI-BF1/PRDM1) promotes differentiation of mature B cells into antibody secreting plasma cells. In contrast ectopic expression of PRDM1 in lymphoma cells can lead to inhibition of proliferation or apoptosis. However, little is currently known about the regulation of PRDM1. The first study presented demonstrates that in lymphoma cells stimulation through the B cell receptor rapidly induces endogenous PRDM1 at the level of transcription. This study provides evidence that the PRDM1 promoter is preloaded and poised for activation in the B c
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Huet, Moulard Émilie. "Étude de la régulation des récepteurs de peptides N-formyles." Université Joseph Fourier (Grenoble), 2007. http://www.theses.fr/2007GRE10077.

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Les cellules phagocytaires constituent la première ligne de défense contre les pathogènes. Leur migration dirigée vers le site infectieux et leurs fonctions microbicides sont l'aboutissement de voies de signalisation intracellulaires sollicitées par la stimulation de récepteurs couplés aux protéines G, les récepteurs de chimioattractants. Après fixation du ligand et transmission du signal par la protéine G, les récepteurs sont phosphorylés et interagissent avec les b-arrestines, protéines d'échafaudage concourrant à l'internalisation des récepteurs. Plusieurs exemples récents suggèrent que les
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Rodríguez, Solovey Leisa Natacha. "IDENTIFICATION OF TARGETS AND AUXILIARY PROTEINS OF PYR/PYL/RCAR ABA RECEPTORS: PROTEIN PHOSPHATASES TYPE 2C (PP2Cs) AND C2-DOMAIN ABA-RELATED PROTEINS (CARs)." Doctoral thesis, Universitat Politècnica de València, 2015. http://hdl.handle.net/10251/58862.

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[EN] ABSTRACT Abscisic acid (ABA) signaling plays a critical role in regulating root growth and root system architecture. ABA-mediated growth promotion and root tropic response under water stress are key responses for plant survival under limiting water conditions. In this work, we have explored the role of Arabidopsis (Arabidopsis thaliana) PYR/PYL/RCAR receptors (PYRABACTIN RESISTANCE1 (PYR1)/PYR1 LIKE (PYL)/REGULATORY COMPONENTS OF ABA RECEPTORS) for root ABA signaling. As a result, we discovered that PYL8 plays a nonredundant role for the regulation of root ABA sensitivity. Unexpectedly,
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Cheng, Lie, and 鄭烈. "Identification of HIV Nucleocapsid Protein Associated Cellular Protein Complexes by Tandem Affinity Purification." Thesis, 2007. http://ndltd.ncl.edu.tw/handle/47673238987183702951.

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碩士<br>國立成功大學<br>分子醫學研究所<br>95<br>A novel Tandem Affinity Purification (TAP) method combined with mass spectrometry (MALDI-TOF, MS) and database search algorithms are adapted to allow identification of HIV NC protein interacting partners. Our preliminary goal is to identify and characterize cellular proteins associated with HIV nucleocapsid (NC) or during precursor Gag trafficking. NC participates in many steps in virus lifecycle, including (1) viral RNA binding and chaperone activity during reverse transcription and cDNA synthesis in the early stages of viral infection and (2) precursor Gag as
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Book chapters on the topic "Tandem-affinity purification"

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Miyoshi, Keita, Akiyo Ogino, Mikiko C. Siomi, and Haruhiko Siomi. "Purification of dFMR1-Containing Complexes Using Tandem Affinity Purification." In Methods in Molecular Biology. Humana Press, 2013. http://dx.doi.org/10.1007/978-1-62703-411-1_8.

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Goodfellow, Ian, and Dalan Bailey. "Detection of Protein–Protein Interactions Using Tandem Affinity Purification." In Protein Affinity Tags. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1034-2_10.

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Viala, Julie P. M., and Emmanuelle Bouveret. "Protein–Protein Interaction: Tandem Affinity Purification in Bacteria." In Methods in Molecular Biology. Springer New York, 2017. http://dx.doi.org/10.1007/978-1-4939-7033-9_18.

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Blackwell, Chris, and Jeremy D. Brown. "The Application of Tandem-Affinity Purification to Candida albicans." In Candida albicans. Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-151-6_13.

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Locatelli-Hoops, Silvia C., and Alexei A. Yeliseev. "Use of Tandem Affinity Chromatography for Purification of Cannabinoid Receptor CB2." In Protein Affinity Tags. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1034-2_9.

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García-León, Marta, Elisa Iniesto, and Vicente Rubio. "Tandem Affinity Purification of Protein Complexes from Arabidopsis Cell Cultures." In Methods in Molecular Biology. Springer New York, 2018. http://dx.doi.org/10.1007/978-1-4939-7871-7_21.

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Zhao, Hongwei, Xinfu Ye, and Qingshun Quinn Li. "Characterization of Plant Polyadenylation Complexes by Using Tandem Affinity Purification." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-2175-1_7.

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Daulat, Avais M., Pascal Maurice, and Ralf Jockers. "Tandem Affinity Purification and Identification of GPCR-Associated Protein Complexes." In Methods in Molecular Biology. Humana Press, 2011. http://dx.doi.org/10.1007/978-1-61779-126-0_23.

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Campden, Rhiannon, Darlaine Pétrin, Mélanie Robitaille, et al. "Tandem Affinity Purification to Identify Cytosolic and Nuclear Gβγ-Interacting Proteins." In Methods in Molecular Biology. Springer New York, 2014. http://dx.doi.org/10.1007/978-1-4939-1755-6_14.

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Bayram, Özgür, Özlem Sarikaya Bayram, Oliver Valerius, Bastian Jöhnk, and Gerhard H. Braus. "Identification of Protein Complexes from Filamentous Fungi with Tandem Affinity Purification." In Fungal Secondary Metabolism. Humana Press, 2012. http://dx.doi.org/10.1007/978-1-62703-122-6_14.

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Conference papers on the topic "Tandem-affinity purification"

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Electricwala, A., and T. Atkinson. "TANDEM PURIFICATION OF TISSUE PLASMINOGEN ACTIVATOR BY METAL CHELATE AND AFFINITY CHROMATOGRAPHY." In XIth International Congress on Thrombosis and Haemostasis. Schattauer GmbH, 1987. http://dx.doi.org/10.1055/s-0038-1644831.

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A tandem purification procedure was developed by a combination of metal chelate and affinity chromatography. The conditioned medium from different cell lines producing tissue plasminogen activator was first chromatographed on a zinc chelate-agarose column equilibrated with low ionic strength buffer. After thorough washing, the column was connected to a lysine-agarose column, previously equilibrated with the same buffer. Tissue plasminogen activator was eluted from the zinc chelate column by a gradient of imidazole and the effluent was allowed to flow through lysine-agarose matrix. The two colu
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Zhao, H., H. Jiang, W. Sun, Z. Shao, and X. Hu. "Abstract P1-06-10: Combined tandem affinity purification mass-spectrometry technique with genome-editing CRISPR-Cas9 knockout screening to identify potential subunits in the BRCA1 complex." In Abstracts: 2018 San Antonio Breast Cancer Symposium; December 4-8, 2018; San Antonio, Texas. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-p1-06-10.

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Reports on the topic "Tandem-affinity purification"

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Chamovitz, Daniel A., and Albrecht G. Von Arnim. eIF3 Complexes and the eIF3e Subunit in Arabidopsis Development and Translation Initiation. United States Department of Agriculture, 2009. http://dx.doi.org/10.32747/2009.7696545.bard.

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The original working hypothesis of our proposal was that The “e” subunit of eIF3 has multiple functions from both within the nucleus and in the cytoplasm. Within this model, we further hypothesized that the “e” subunit of eIF3 functions in translation as a repressor. We proposed to test these hypotheses along the following specific aims: 1) Determine the subcellular localization of the interaction between eIF3e and other eIF3 subunits, or the COP9 signalosome. 2) Elucidate the biological significance of the varied subcellular localizations of eIF3e through generating Arabidopsis eIF3e alleles
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