Nanobody (37 Ergebnisse)

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

Paperback or Softback. Zustand: New. A toolkit to study nuclear transport pathways: nanobody-mediated inhibition of importin ?-related nuclear transport receptors (NTRs). Book.

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

PAP. Zustand: New. New Book. Shipped from UK. Established seller since 2000.

Zustand: New.

Zustand: New.

Zustand: New.

Zustand: As New. Unread book in perfect condition.

Hardback. Zustand: New.

Zustand: New.

Zustand: New. In English.

Zustand: As New. Unread book in perfect condition.

Hardback. Zustand: New.

Paperback. Zustand: Like New. LIKE NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Hardcover. Zustand: New. NEW. SHIPS FROM MULTIPLE LOCATIONS. book.

Taschenbuch. Zustand: Neu. Anti-Schistosoma Nanobody Conjugate: A Novel Theranostic Tool | Single-Domain Antibody-Nanoparticles Conjugate: A Novel Tool for Diagnostic and Therapeutic Application | Mohamed Sallam | Taschenbuch | 144 S. | Englisch | 2013 | LAP LAMBERT Academic Publishing | EAN 9783659385681 | Verantwortliche Person für die EU: preigu GmbH & Co. KG, Lengericher Landstr. 19, 49078 Osnabrück, mail[at]preigu[dot]de | Anbieter: preigu.…

Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 136 pp. Englisch.

HRD. Zustand: New. New Book. Shipped from UK. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware -Nanobodies are recombinant single-domain antibodies of camelid origin. We set out to generate nanobodies as tools to study nuclear pore complexes (NPCs) that constitute the major passageways for nucleocytoplasmic exchange. Therefore, we developed an optimized phage display-based workflow for the generation of nanobodies from an immunized animal. The identified nanobodies were functionally expressed in the E. coli cytoplasm in a disulfide bond-free form, thus overcoming the engineering limitations imposed by conventional periplasmic secretion. Using protease-cleavable affinity tags, we developed a generic strategy for native protein complex isolation from eukaryotic sources, e.g. for structural analyses by electron microscopy. We further established a reliable fluorescent labeling strategy of nanobodies that is based on engineered surface cysteines and maleimide chemistry. In contrast to NHS labeling of lysines, maleimide labeling is site-specific, does not interfere with antigen recognition and yields superior imaging reagents, especially for super-resolution microscopy. Using our optimized workflow, we obtained a large toolbox of nanobodies against constituents of Xenopus NPCs that can now be used to study various unresolved aspects of NPC structure, assembly and function. 154 pp. Deutsch.…

HRD. Zustand: New. New Book. Delivered from our UK warehouse in 4 to 14 business days. THIS BOOK IS PRINTED ON DEMAND. Established seller since 2000.

Taschenbuch. Zustand: Neu. This item is printed on demand - it takes 3-4 days longer - Neuware 144 pp. Englisch.

Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. KlappentextrnrnNanobodies are recombinant single-domain antibodies of camelid origin. We set out to generate nanobodies as tools to study nuclear pore complexes (NPCs) that constitute the major passageways for nucleocytoplasmic exchange. Therefo.…

Zustand: New. Print on Demand pp. 300.

Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Eukaryotic cells are divided into a nuclear and a cytoplasmic compartment. This separates transcription from translation and makes gene expression dependent on nucleocytoplasmic transport. The members of the importin ß superfamily function as shuttling nuclear transport receptors (NTRs) that recognize and actively transport cargoes through nuclear pores. An estimated 5 000 to 10 000 different human proteins are subject to active nuclear transport. Numerous cargo/NTR pairs have been identified, however, we are still far from a complete understanding as it has been very challenging to setup a systematic in vivo analysis that integrates the impact of all transport pathways.In this study, we obtained anti-NTR nanobodies against TRN1, Xpo4, Xpo7, and CAS. Our aim was to identify nanobodies, and prepare nanobody fusions, that impede nuclear pore-passage of the targeted NTR and thus, interrupt a given transport cycle. These nanobody fusions were observed to inhibit the partition of NTR/cargo complexes into a reconstituted FG phase. We also observed that the nanobodies and nanobody fusions inhibit NTR transport in permeabilized cells.…

Zustand: New. Dieser Artikel ist ein Print on Demand Artikel und wird nach Ihrer Bestellung fuer Sie gedruckt. Autor/Autorin: Sallam MohamedMohamed Sallam is an Egyptian researcher at the DKFZ, Heidelberg, Germany. He has a B.Sc. in Biochemistry and an M.Sc. in Nanotechnology. During his research he applied many state-of-the-art techniques for the utilizati.…

Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Eukaryotic cells are divided into a nuclear and a cytoplasmic compartment. This separates transcription from translation and makes gene expression dependent on nucleocytoplasmic transport. The members of the importin ß superfamily function as shuttling nuclear transport receptors (NTRs) that recognize and actively transport cargoes through nuclear pores. An estimated 5 000 to 10 000 different human proteins are subject to active nuclear transport. Numerous cargo/NTR pairs have been identified, however, we are still far from a complete understanding as it has been very challenging to setup a systematic in vivo analysis that integrates the impact of all transport pathways.In this study, we obtained anti-NTR nanobodies against TRN1, Xpo4, Xpo7, and CAS. Our aim was to identify nanobodies, and prepare nanobody fusions, that impede nuclear pore-passage of the targeted NTR and thus, interrupt a given transport cycle. These nanobody fusions were observed to inhibit the partition of NTR/cargo complexes into a reconstituted FG phase. We also observed that the nanobodies and nanobody fusions inhibit NTR transport in permeabilized cells.Cuvillier Verlag, Nonnenstieg 8, 37075 Göttingen 136 pp. Englisch.…

Zustand: New. Print on Demand pp. 300.

Taschenbuch. Zustand: Neu. nach der Bestellung gedruckt Neuware - Printed after ordering - Nanobodies are recombinant single-domain antibodies of camelid origin. We set out to generate nanobodies as tools to study nuclear pore complexes (NPCs) that constitute the major passageways for nucleocytoplasmic exchange. Therefore, we developed an optimized phage display-based workflow for the generation of nanobodies from an immunized animal. The identified nanobodies were functionally expressed in the E. coli cytoplasm in a disulfide bond-free form, thus overcoming the engineering limitations imposed by conventional periplasmic secretion. Using protease-cleavable affinity tags, we developed a generic strategy for native protein complex isolation from eukaryotic sources, e.g. for structural analyses by electron microscopy. We further established a reliable fluorescent labeling strategy of nanobodies that is based on engineered surface cysteines and maleimide chemistry. In contrast to NHS labeling of lysines, maleimide labeling is site-specific, does not interfere with antigen recognition and yields superior imaging reagents, especially for super-resolution microscopy. Using our optimized workflow, we obtained a large toolbox of nanobodies against constituents of Xenopus NPCs that can now be used to study various unresolved aspects of NPC structure, assembly and function.…

Taschenbuch. Zustand: Neu. This item is printed on demand - Print on Demand Titel. Neuware -Nanobodies are recombinant single-domain antibodies of camelid origin. We set out to generate nanobodies as tools to study nuclear pore complexes (NPCs) that constitute the major passageways for nucleocytoplasmic exchange. Therefore, we developed an optimized phage display-based workflow for the generation of nanobodies from an immunized animal. The identified nanobodies were functionally expressed in the E. coli cytoplasm in a disulfide bond-free form, thus overcoming the engineering limitations imposed by conventional periplasmic secretion. Using protease-cleavable affinity tags, we developed a generic strategy for native protein complex isolation from eukaryotic sources, e.g. for structural analyses by electron microscopy. We further established a reliable fluorescent labeling strategy of nanobodies that is based on engineered surface cysteines and maleimide chemistry. In contrast to NHS labeling of lysines, maleimide labeling is site-specific, does not interfere with antigen recognition and yields superior imaging reagents, especially for super-resolution microscopy. Using our optimized workflow, we obtained a large toolbox of nanobodies against constituents of Xenopus NPCs that can now be used to study various unresolved aspects of NPC structure, assembly and function.Cuvillier Verlag, Nonnenstieg 8, 37075 Göttingen 154 pp. Deutsch.…