Preparation and Characterization of Novel Quaternized Cellulose Nanoparticles as Protein Carriers

2009 ◽  
Vol 9 (9) ◽  
pp. 857-863 ◽  
Author(s):  
Yongbo Song ◽  
Jinping Zhou ◽  
Qian Li ◽  
Yi Guo ◽  
Lina Zhang
Keyword(s):  
Cellulose Nanoparticles ◽  
Protein Carriers

Characterization of films made with chayote tuber and potato starches blending with cellulose nanoparticles

2013 ◽  
Vol 98 (1) ◽  
pp. 102-107 ◽  
Author(s):  
Selene Aila-Suárez ◽  
Heidi M. Palma-Rodríguez ◽  
Adriana I. Rodríguez-Hernández ◽  
Juan P. Hernández-Uribe ◽  
Luis A. Bello-Pérez ◽  
...  
Keyword(s):  
Cellulose Nanoparticles ◽  
Potato Starches

scholarly journals Identification of blood-protein carriers of the CA 19-9 antigen and characterization of prevalence in pancreatic diseases

PROTEOMICS ◽  
2011 ◽  
Vol 11 (18) ◽  
pp. 3665-3674 ◽  
Author(s):  
Tingting Yue ◽  
Katie Partyka ◽  
Kevin A. Maupin ◽  
Mary Hurley ◽  
Philip Andrews ◽  
...  
Keyword(s):  
Blood Protein ◽  
Pancreatic Diseases ◽  
Protein Carriers

scholarly journals Production and characterization of cellulose nanoparticles from nopal waste by means of high impact milling

2017 ◽  
Vol 200 ◽  
pp. 428-433 ◽  
Author(s):  
M.Q. Marin-Bustamante ◽  
J.J. Chanona-Pérez, ◽  
N Güemes-Vera ◽  
R. Cásarez-Santiago ◽  
M. J PereaFlores ◽  
...  
Keyword(s):  
High Impact ◽  
Cellulose Nanoparticles ◽  
Impact Milling

Chapter 4. Characterization of Cellulose Nanoparticles

2021 ◽  
pp. 86-112
Author(s):  
L. Buzón-Durán ◽  
J. Martín-Gil ◽  
P. Martín-Ramos
Keyword(s):  
Cellulose Nanoparticles

Morphological Characterization of Mycobacteriophage R1

1974 ◽  
Vol 32 ◽  
pp. 254-255
Author(s):  
B. L. Soloff ◽  
T. A. Rado
Keyword(s):  
Carbon Source ◽  
Stationary Phase ◽  
Growth Phase ◽  
Minimal Medium ◽  
Morphological Characterization ◽  
Logarithmic Growth Phase ◽  
Complete Lysis ◽  
Lysogenic Culture ◽  
Logarithmic Growth

Mycobacteriophage R1 was originally isolated from a lysogenic culture of M. butyricum. The virus was propagated on a leucine-requiring derivative of M. smegmatis, 607 leu−, isolated by nitrosoguanidine mutagenesis of typestrain ATCC 607. Growth was accomplished in a minimal medium containing glycerol and glucose as carbon source and enriched by the addition of 80 μg/ ml L-leucine. Bacteria in early logarithmic growth phase were infected with virus at a multiplicity of 5, and incubated with aeration for 8 hours. The partially lysed suspension was diluted 1:10 in growth medium and incubated for a further 8 hours. This permitted stationary phase cells to re-enter logarithmic growth and resulted in complete lysis of the culture.

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