scholarly journals Solubilization and Characterization of the Residual Proteins of the Cell Nucleus

1966 ◽  
Vol 241 (12) ◽  
pp. 2913-2917
Author(s):  
Tung Yue Wang
Keyword(s):  
Cell Nucleus

scholarly journals Characterization of the P Protein-Binding Domain on the 10-Kilodalton Protein of Borna Disease Virus

2000 ◽  
Vol 74 (7) ◽  
pp. 3413-3417 ◽  
Author(s):  
Tahir H. Malik ◽  
Masahiko Kishi ◽  
Patrick K. Lai
Keyword(s):  
Disease Virus ◽  
Nuclear Localization ◽  
Cell Nucleus ◽  
Binding Domain ◽  
Borna Disease Virus ◽  
Nuclear Localization Signals ◽  
P Protein ◽  
Infected Cells ◽  
Borna Disease

ABSTRACT The Borna disease virus (BDV) is the prototype member of the Bornaviridae, and it replicates in the cell nucleus. The BDV p24P and p40N proteins carry nuclear localization signals (NLS) and are found in the nuclei of infected cells. The BDV p10 protein does not have an NLS, but it binds with P and/or N and is translocated to the nucleus. Hence, p10 may play a role in the replication of BDV in the cell nucleus. Here, we show that the P-binding domain is located in the N terminus of p10 and that S3 and L16 are important for the interaction.

Characterization of an In Vivo Z-DNA Detection Probe Based on a Cell Nucleus Accumulating Intrabody

2016 ◽  
Vol 58 (8-9) ◽  
pp. 585-594 ◽  
Author(s):  
Galina Gulis ◽  
Izabel Cristina Rodrigues Silva ◽  
Herdson Renney Sousa ◽  
Isabel Garcia Sousa ◽  
Maryani Andressa Gomes Bezerra ◽  
...  
Keyword(s):  
Cell Nucleus ◽  
Dna Detection ◽  
Detection Probe ◽  
A Cell ◽  
Z Dna

scholarly journals Morphometry and morphology of nucleus of the Sertoli and interstitial cells of the tambaqui Colossoma macropomum (Cuvier, 1881) (Pisces: Characidae) during the reproductive cycle

2003 ◽  
Vol 63 (1) ◽  
pp. 97-104 ◽  
Author(s):  
L. S. O. Nakaghi ◽  
D. Mitsuiki ◽  
H. S. L. Santos ◽  
M. R. Pacheco ◽  
L. N. Ganeco
Keyword(s):  
Sertoli Cell ◽  
Reproductive Cycle ◽  
Cell Nucleus ◽  
Sertoli Cells ◽  
Structural Organization ◽  
Interstitial Cells ◽  
Interstitial Tissue ◽  
Colossoma Macropomum ◽  
Tissue Area

This study allowed the characterization of the tambaqui Colossoma macropomum testes structural organization, emphasizing Sertoli and interstitial cells and analyzing morphometrically the Sertoli cell nucleus diameter and the interstitial tissue area during the reproductive cycle. Fragments of tambaqui testes were collected in the following reproductive cycle stages: immature, resting, maturation I and II, mature, and regression, and were histologically processed. The Sertoli cells were found at the periphery of the cysts of germinative lineage cells and the nuclei were shown to be smaller as these cells developed. The interstitial cells were better observed between the seminiferous lobules next to vessels in the interstitial tissue of maturing testes.

In Situ Mechanical Characterization of the Cell Nucleus by Atomic Force Microscopy

ACS Nano ◽  
2014 ◽  
Vol 8 (4) ◽  
pp. 3821-3828 ◽  
Author(s):  
Haijiao Liu ◽  
Jun Wen ◽  
Yun Xiao ◽  
Jun Liu ◽  
Sevan Hopyan ◽  
...  
Keyword(s):  
Atomic Force Microscopy ◽  
Cell Nucleus ◽  
Mechanical Characterization ◽  
Force Microscopy ◽  
Atomic Force

scholarly journals Image analysis and definition of nuclear phenotypes

1997 ◽  
Vol 20 (4) ◽  
pp. 749-754 ◽  
Author(s):  
Benedicto de Campos Vidal
Keyword(s):  
Image Analysis ◽  
Cell Nucleus ◽  
Geometric Information ◽  
Definition Of

Some basic topics concerned with the extraction of textural and geometric information from cell nucleus images as well as description and characterization of chromatin supraorganization and consequent classification of nuclear phenotypes are presented.

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.

AEM analysis of crystallization in Ti-based amorphous alloys

1983 ◽  
Vol 41 ◽  
pp. 270-271
Author(s):  
A.R. Pelton ◽  
A.F. Marshall ◽  
Y.S. Lee
Keyword(s):  
Magnetic Properties ◽  
Amorphous Alloys ◽  
Amorphous Materials ◽  
Isothermal Annealing ◽  
Amorphous Matrix ◽  
Nucleation And Growth ◽  
Current Interest ◽  
Amorphous Films ◽  
Electrical And Magnetic Properties

Amorphous materials are of current interest due to their desirable mechanical, electrical and magnetic properties. Furthermore, crystallizing amorphous alloys provides an avenue for discerning sequential and competitive phases thus allowing access to otherwise inaccessible crystalline structures. Previous studies have shown the benefits of using AEM to determine crystal structures and compositions of partially crystallized alloys. The present paper will discuss the AEM characterization of crystallized Cu-Ti and Ni-Ti amorphous films.Cu60Ti40: The amorphous alloy Cu60Ti40, when continuously heated, forms a simple intermediate, macrocrystalline phase which then transforms to the ordered, equilibrium Cu3Ti2 phase. However, contrary to what one would expect from kinetic considerations, isothermal annealing below the isochronal crystallization temperature results in direct nucleation and growth of Cu3Ti2 from the amorphous matrix.

Sign in / Sign up

Export Citation Format

Share Document