Hochschulschrift
A high-throughput compatible cell-free protein fragment complementation assay monitoring viral protein interactions
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Anmerkungen
-
München, Ludwig-Maximilians-Universität, Diss., 2012
- Schlagwort
-
Arzneimittelentwicklung
Arzneimitteldesign
- Ereignis
-
Veröffentlichung
- (wo)
-
München
- (wer)
-
Universitätsbibliothek der Ludwig-Maximilians-Universität
- (wann)
-
2012
- Urheber
-
Wagner, Felicia
- Beteiligte Personen und Organisationen
-
Hopfner, Karl-Peter
- URN
-
urn:nbn:de:bvb:19-175101
- Rechteinformation
-
Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
25.03.2025, 13:52 MEZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Objekttyp
- Hochschulschrift
Beteiligte
- Wagner, Felicia
- Hopfner, Karl-Peter
- Universitätsbibliothek der Ludwig-Maximilians-Universität
Entstanden
- 2012
Ähnliche Objekte (12)
Optimization of Protein Production Development Using a Combination of Cell-Free Expression and High-Throughput Protein Analysis
A High-Throughput Analysis of Circadian Protein Stability
A high-throughput analysis of circadian protein stability
Development and application of a high-throughput cell-free expression system
Development and application of a high-throughput cell-free expression system
Algorithm to identify protein complexes from high-throughput data
Using high-throughput methods to chart protein-protein and protein-lipid interactions in eukaryotic cells
USING HIGH‐THROUGHPUT METHODS TO CHART PROTEIN‐PROTEIN AND PROTEIN‐LIPID INTERACTIONS IN EUKARYOTIC CELLS
High-throughput experimentation for microscale cultivations and recombinant protein expression
What do we learn from high-throughput protein interaction data?
High-throughput screening of protein-protein-interactions in Mammalian Cells using transfected cell arrays
Fast iodide-SAD phasing for high-throughput membrane protein structure determination
Optimization of Protein Production Development Using a Combination of Cell-Free Expression and High-Throughput Protein Analysis
A High-Throughput Analysis of Circadian Protein Stability
A high-throughput analysis of circadian protein stability
Development and application of a high-throughput cell-free expression system
Development and application of a high-throughput cell-free expression system
Algorithm to identify protein complexes from high-throughput data
Using high-throughput methods to chart protein-protein and protein-lipid interactions in eukaryotic cells
USING HIGH‐THROUGHPUT METHODS TO CHART PROTEIN‐PROTEIN AND PROTEIN‐LIPID INTERACTIONS IN EUKARYOTIC CELLS
High-throughput experimentation for microscale cultivations and recombinant protein expression
What do we learn from high-throughput protein interaction data?
High-throughput screening of protein-protein-interactions in Mammalian Cells using transfected cell arrays
Fast iodide-SAD phasing for high-throughput membrane protein structure determination
Optimization of Protein Production Development Using a Combination of Cell-Free Expression and High-Throughput Protein Analysis
A High-Throughput Analysis of Circadian Protein Stability
A high-throughput analysis of circadian protein stability
Development and application of a high-throughput cell-free expression system
Development and application of a high-throughput cell-free expression system
Algorithm to identify protein complexes from high-throughput data
Using high-throughput methods to chart protein-protein and protein-lipid interactions in eukaryotic cells
USING HIGH‐THROUGHPUT METHODS TO CHART PROTEIN‐PROTEIN AND PROTEIN‐LIPID INTERACTIONS IN EUKARYOTIC CELLS
High-throughput experimentation for microscale cultivations and recombinant protein expression
What do we learn from high-throughput protein interaction data?
High-throughput screening of protein-protein-interactions in Mammalian Cells using transfected cell arrays