Ploidy Determination of Parthenogenetic Artemia by Flow Cytometry

2011 ◽  
Vol 474-476 ◽  
pp. 605-608
Author(s):  
Su Feng Wang ◽  
Yan Wang

The ploidy of parthenogenetic Artemia from Aqqikkol Hu (Xinjiang) was determinated by flow cytometry. The results showed that the Artemia populaton of Aqqikkol Hu (Xinjiang) consisted diploid and tetraploid, the rate of diploid and tetraploid approximated to 80% and 20% respectively. It should conclude that the results of ploidy of parthenogenetic Artemia can be determinated rapidly and exactly by flow cytometry. The new method for the ploidy determination of parthenogenetic Artemia should accumulate the basic data for biological study and application of Artemia.

Crop Science ◽  
1999 ◽  
Vol 39 (4) ◽  
pp. 1202-1207 ◽  
Author(s):  
E. Charles Brummer ◽  
Patricia M. Cazcarro ◽  
Diane Luth

Crop Science ◽  
2001 ◽  
Vol 41 (5) ◽  
pp. 1629-1634 ◽  
Author(s):  
Metin Tuna ◽  
Kenneth P. Vogel ◽  
K. Arumuganathan ◽  
Kulvinder S. Gill

Cytometry ◽  
1998 ◽  
Vol 32 (3) ◽  
pp. 186-190 ◽  
Author(s):  
Jean-Marc Navenot ◽  
Taha Merghoub ◽  
Rolande Ducrocq ◽  
Jean-Yves Muller ◽  
Rajagopal Krishnamoorthy ◽  
...  

1960 ◽  
Vol 23 ◽  
pp. 227-232 ◽  
Author(s):  
P WEST ◽  
G LYLES
Keyword(s):  

1977 ◽  
Vol 37 (02) ◽  
pp. 210-215 ◽  
Author(s):  
R Margalit ◽  
E Gidron ◽  
Y Shalitin

SummaryThe term “effective activator” of plasminogen is proposed, to denote the resultant of activator-antiactivator interaction, and a method for the determination of the level of these activators is described. By adding axcess plasminogen to the euglobulin fraction of plasma the influence of the level of endogenous plasminogen and of the antiplasmin is eliminated. It is shown that the level of fibrinogen has very little bearing on the results. An effective activator unit is defined as equal to 1 CTA unit of urokinase activity on a fibrinogen-plasminogen substrate.


1964 ◽  
Vol 12 (01) ◽  
pp. 119-125 ◽  
Author(s):  
Y Shamash ◽  
A Rimon

SummaryA new method for the assay of plasmin inhibitors in human plasma is described. The method consists of determination of the caseinolytic activity of a standard plasmin solution before and after incubation with the inhibitor, with lysine added to the mixture as a stabilizer of plasmin. Using this method, it was found that plasma contains enough inhibitors to inactivate 30 caseinolytic units of plasmin, or 10 times the normal amount of plasminogen in human plasma.


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