Mass action analysis of kinetics and extent of fusion between Sendai virus and phospholipid vesicles

Biochemistry ◽  
1986 ◽  
Vol 25 (25) ◽  
pp. 8261-8266 ◽  
Author(s):  
Shlomo Nir ◽  
Karin Klappe ◽  
Dick Hoekstra
Keyword(s):  
Sendai Virus ◽  
Mass Action ◽  
Phospholipid Vesicles ◽  
Action Analysis

scholarly journals Controlling A-center concentration in silicon through isovalent doping: mass action analysis

2016 ◽  
Vol 27 (5) ◽  
pp. 4385-4391 ◽  
Author(s):  
S.-R. G. Christopoulos ◽  
D. C. Parfitt ◽  
E. N. Sgourou ◽  
C. A. Londos ◽  
R. V. Vovk ◽  
...  
Keyword(s):  
Mass Action ◽  
Isovalent Doping ◽  
Action Analysis

Fusion of influenza virus with cardiolipin liposomes at low pH: mass action analysis of kinetics and extent

Biochemistry ◽  
1986 ◽  
Vol 25 (1) ◽  
pp. 257-266 ◽  
Author(s):  
S. Nir ◽  
T. Stegmann ◽  
J. Wilschut
Keyword(s):  
Influenza Virus ◽  
Low Ph ◽  
Mass Action ◽  
Action Analysis

scholarly journals Bulk Fusion Studies of Sendai Virus and Application of Mass Action Kinetic Fusion Model

2021 ◽  
Vol 120 (3) ◽  
pp. 320a
Author(s):  
Papa Freduah A. Anderson ◽  
Robert J. Rawle
Keyword(s):  
Sendai Virus ◽  
Mass Action ◽  
Fusion Model ◽  
Mass Action Kinetic

Electron Microscope Study of RNA's of Paramyxoviruses

1972 ◽  
Vol 30 ◽  
pp. 196-197
Author(s):  
Ruchama Baum ◽  
J.T. Seto
Keyword(s):  
Electron Microscopy ◽  
Electron Microscope ◽  
Electron Microscope Study ◽  
Sendai Virus ◽  
Sodium Dodecyl ◽  
Rna Molecules ◽  
Virus Particles ◽  
Molecular Weights ◽  
Length Measurements

The ribonucleic acid (RNA) of paramyxoviruses has been characterized by biochemical and physiochemical methods. However, paramyxovirus RNA molecules have not been studied by electron microscopy. The molecular weights of these single-stranded viral RNA molecules are not known as yet. Since electron microscopy has been found to be useful for the characterization of single-stranded RNA, this investigation was initiated to examine the morphology and length measurements of paramyxovirus RNA's.Sendai virus Z strain and Newcastle disease virus (NDV), Milano strain, were used. For these studies it was necessary to develop a method of extracting RNA molecules from purified virus particles. Highly purified Sendai virus was treated with pronase (300 μg/ml) at 37°C for 30 minutes and the RNA extracted by the sodium dodecyl sulfate (SDS)-phenol procedure.

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