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Volumn 76, Issue 2, 2012, Pages 388-390
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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
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Author keywords
Fluorescent protein (FP); Importin alpha (importin ); Nuclear pore complex (NPC); Venus; Weak dimer
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Indexed keywords
DIMER INTERFACE;
ENHANCED GREEN FLUORESCENT PROTEIN;
FLUORESCENT PROTEIN;
FUSION TAG;
HYDROPHOBIC INTERACTIONS;
LIVING CELL;
MAMMALIAN CELLS;
MONOMERIZATION;
NUCLEAR-PORE COMPLEX (NPC);
PHYSIOLOGICAL CONDITION;
SIMPLE METHOD;
SINGLE MUTATION;
VENUS;
DIMERS;
FLUORESCENCE;
PROTEINS;
DIAGNOSTIC AGENT;
ENHANCED GREEN FLUORESCENT PROTEIN;
GREEN FLUORESCENT PROTEIN;
HYBRID PROTEIN;
KARYOPHERIN ALPHA;
PHOTOPROTEIN;
ANIMAL;
ARTICLE;
CELLS;
CHEMICAL PHENOMENA;
CHEMISTRY;
CYTOLOGY;
GENETICS;
METHODOLOGY;
MISSENSE MUTATION;
PROCEDURES;
PROTEIN MULTIMERIZATION;
ALPHA KARYOPHERINS;
ANIMALS;
CELLS;
CYTOLOGICAL TECHNIQUES;
GREEN FLUORESCENT PROTEINS;
HYDROPHOBIC AND HYDROPHILIC INTERACTIONS;
LUMINESCENT PROTEINS;
METHODS;
MUTATION, MISSENSE;
PROTEIN MULTIMERIZATION;
RECOMBINANT FUSION PROTEINS;
MAMMALIA;
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EID: 84857859016
PISSN: 09168451
EISSN: 13476947
Source Type: Journal
DOI: 10.1271/bbb.110677 Document Type: Article |
Times cited : (9)
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References (18)
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