Titlebook: Viral Applications of Green Fluorescent Protein; Methods and Protocol Barry W. Hicks Book 2009 The Editor(s) (if applicable) and The Author

Taylor

書目名稱Viral Applications of Green Fluorescent Protein影響因子(影響力)




書目名稱Viral Applications of Green Fluorescent Protein影響因子(影響力)學(xué)科排名




書目名稱Viral Applications of Green Fluorescent Protein網(wǎng)絡(luò)公開度




書目名稱Viral Applications of Green Fluorescent Protein網(wǎng)絡(luò)公開度學(xué)科排名




書目名稱Viral Applications of Green Fluorescent Protein被引頻次




書目名稱Viral Applications of Green Fluorescent Protein被引頻次學(xué)科排名




書目名稱Viral Applications of Green Fluorescent Protein年度引用




書目名稱Viral Applications of Green Fluorescent Protein年度引用學(xué)科排名




書目名稱Viral Applications of Green Fluorescent Protein讀者反饋




書目名稱Viral Applications of Green Fluorescent Protein讀者反饋學(xué)科排名

槍支

Using Fluorescent Proteins to Study Poxvirus Morphogenesis,croscopy for analysis of the FP pattern. The methods presented here describe how to infect and transfect cells for trans-complementation for the purpose of functional domain mapping. The imaging and analysis of these cells is described.

arcane

Molecular Imaging of Human Embryonic Stem Cells,modalities made available by use of this construct, including optical fluorescence, bioluminescence, and positron emission tomography (PET), may be adapted to investigate a variety of physiological phenomena, including the spatio-temporal kinetics of hESC engraftment and proliferation in living subj

無價(jià)值

裹住

場所

Tracheotomy

Inoperable

航海太平洋

Modified Bovine Herpesvirus 1 for Protein Secretion,biquitously present endoprotease furin. The general applicability of this novel expression strategy is demonstrated by using GFP as reporter protein to monitor secretion. We hypothesize that also other secreted or membrane-bound (glyco)proteins can be engineered to function as transporters for oligo

Ergots

Use of GFP to Investigate Expression of Plant-Derived Vaccines,co leaves. The GFP tag enables a relatively quick confirmation of antigen expression in plant cells by fluorescent microscopy. Such analysis using GFP that precedes stable plant transformation will enable the rapid screening of multiple constructs to attain optimal recombinant protein expression. Fu