A new method for sex determination of the donor of forensic samples using a recombinant DNA probe

1987 ◽  
Vol 8 (1) ◽  
pp. 35-38 ◽  
Author(s):  
Peter Gill
Keyword(s):  
Sex Determination ◽  
Recombinant Dna ◽  
Dna Probe ◽  
New Method ◽  
Forensic Samples

Sex determination of forensic samples by dual PCR amplification of an X-Y homologous gene

1992 ◽  
Vol 52 (2) ◽  
pp. 143-148 ◽  
Author(s):  
Atsushi Akane ◽  
Satoko Seki ◽  
Hiroshi Shiono ◽  
Hiroaki Nakamura ◽  
Masanori Hasegawa ◽  
...  
Keyword(s):  
Sex Determination ◽  
Pcr Amplification ◽  
Homologous Gene ◽  
Forensic Samples

A new method for the determination of nitrates

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

A New Method for the Determination of Plasma Activators of Fibrinolysis

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

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.

The Plasmin Inhibitors of Plasma

1964 ◽  
Vol 12 (01) ◽  
pp. 119-125 ◽  
Author(s):  
Y Shamash ◽  
A Rimon
Keyword(s):  
Human Plasma ◽  
New Method ◽  
Normal Amount ◽  
Caseinolytic Activity ◽  
Before And After ◽  
Plasmin Inhibitors

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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