A Rapid and Simple Method of Evaluating the Dimeric Tendency of Fluorescent Proteins in Living Cells Using a Truncated Protein of Importin α as Fusion Tag
スポンサーリンク
概要
- 論文の詳細を見る
- 2012-02-23
著者
-
SENDA-MURATA Kaori
Laboratory of Molecular Biology and Cell Informatics, Division of Bioscience and Informatics, Gradua
-
Sugimoto Kenji
Laboratory Of Molecular Biology And Cell Informatics Graduate School Of Life And Environmental Scien
-
Nishimura Shigenori
Laboratory Of Biophysical Chemistry College Of Agriculture Osaka Prefecture University
-
Sugimoto Kenji
Laboratory Of Applied Molecular Biology Department Of Applied Biochemistry Osaka Prefecture Universi
-
Nakagawa Chika
Laboratory Of Molecular Biology And Cell Informatics Division Of Bioscience And Informatics Graduate
-
Sugimoto Kenji
Laboratory Of Molecular Biology And Cell Informatics Division Of Bioscience And Informatics Graduate
-
Nishimura Shigenori
Laboratory Of Molecular Biology And Cell Informatics Division Of Bioscience And Informatics Graduate
-
Senda Murata
Laboratory Of Molecular Biology And Cell Informatics Division Of Bioscience And Informatics Graduate School Of Life And Environmental Sciences Osaka Prefecture University
関連論文
- Syntheses of α-Arbutin-α-Glycosides and Their Inhibitory Effects on Human Tyrosinase(Enzymology, Protein Engineering, and Enzyme Technology)
- Inhibitory Effects of α-Arbutin on Melanin Synthesis in Cultured Human Melanoma Cells and a Three-Dimensional Human Skin Model (Pharmacology)
- Syntheses of Arbutin-α-glycosides and a Comparison of Their Inhibitory Effects with Those of α-Arbutin and Arbutin on Human Tyrosinase
- Centromere/Kinetochore Localization of Human Centromere Protein A (CENP-A) Exogenously Expressed as a Fusion to Green Fluorescent Protein
- Functional Domain Structure of Human Heterochromatin Protein HP1^ : Involvement of Internal DNA-Binding and C-Terminal Self-Association Domains in the Formation of Discrete Dots in Interphase Nuclei
- Human Homolog of Drosophila Heterochromatin-Associated Protein 1 (HP1) Is a DNA-Binding Protein Which Possesses a DNA-Binding Motif with Weak Similarity to That of Human Centromere Protein C(CENP-C)
- Molecular Dynamics of Aurora-A Kinase in Living Mitotic Cells Simultaneously Visualized with Histone H3 and Nuclear Membrane Protein Importinα
- cDNA Cloning of the Cry1Aa Receptor Variants from Bombyx mori and Their Expression in Mammalian Cells
- Rhythmic Cycle of Clathrin-Coated Pit Formation at the trans-Golgi Network in Human MDA-MB-435 Cells
- Visualization of Aberrant Perinuclear Microtubule Aster Organization by Microtubule-Destabilizing Agents
- A Multi-Fluorescent MDA435 Cell Line for Mitosis Inhibitor Studies : Simultaneous Visualization of Chromatin, Microtubules, and Nuclear Envelope in Living Cells
- Dynamic Behavior of FCHO1 Revealed by Live-Cell Imaging Microscopy : Its Possible Involvement in Clathrin-Coated Vesicle Formation
- Rhythmic Cycle of Clathrin-Coated Pit Formation at the trans-Golgi Network in Human MDA-MB-435 Cells
- An Antigenic Determinant on Human Centromere Protein B (CENP-B) Available for Production of Human-Specific Anticentromere Antibodies in Mouse
- Casein Kinase II Site of Human Centromere Protein B (CENP-B) is Phosphorylated in Vitro
- Improvement of a Venus-Based Bimolecular Fluorescence Complementation Assay to Visualize bFos-bJun Interaction in Living Cells
- Maltal Binding Mechanism and a Role of the Mobile Loop of Soybean β-Amylase
- Two Additional Carbohydrate-Binding Sites of β-Amylase from Bacillus cereus var. mycoides Are Involved in Hydrolysis and Raw Starch-Binding
- Catalytic Mechanism of β-Amylase from Bacillus cereus var. mycoides : Chemical Rescue of Hydrolytic Activity for a Catalytic Site Mutant Glu367→Ala) by Azide
- Molecular Behavior in Living Mitotic Cells of Human Centromere Heterochromatin Protein HP1α Ectopically Expressed as a Fusion to Red Fluorescent Protein
- Improvement of a Venus-Based Bimolecular Fluorescence Complementation Assay to Visualize bFos-bJun Interaction in Living Cells
- A Rapid and Simple Method of Evaluating the Dimeric Tendency of Fluorescent Proteins in Living Cells Using a Truncated Protein of Importin α as Fusion Tag