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Certain herbicides (e.g., sodium arsenite) are sometimes applied by the jar method, whereby the tops of weeds are bent over and immersed in jars of poisonous solution.
Coagulation was conducted using jar method with different coagulant dose and at different pHs.
Briefly, infected blood cells (1% parasitemia) were cultured using the Candle Jar method in 24 wells culture plates containing serial drug dilutions of either WR99210[25] (Jacobus Pharmaceutical Company) or blasticidin[7] (Invitrogen).
The microaerophilic conditions were obtained using the candle jar method [ 23].
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Normally, studies of scale formation have been focused on precipitation processes in the bulk solution using bulk jar methods where the precipitation tendency rate and inhibitor effectiveness are quantified.
Stock culture of malaria parasite Plasmodium falciparum 3D7 strain was continuously maintained in vitro using the candle-jar method [30].
Synchronous parasites were prepared [31] to obtain parasitized cells harbouring only the ring stage and challenged with a graded concentration ranging from 0.1 to 10 µg/mL of the drug solution for 48 h at 37 °C by the candle-jar method [30].
Using the Petri dish candle-jar method, parasites were cultured in vitro in complete medium, i.e. RPMI-1640 medium supplemented with 25 mM Hepes (Gibco) and 10% AB+ human serum [16].
Its excellent flocculated decolorization properties were evaluated with Acid Light Yellow 2G solutions using a jar test method.
The JAR locating method assumed that all joints were revolute, however the spread locations of JARs suggested that, for instance in the hip and stifle joints, slight cranio-caudal translation may also have occurred.
The point of subculture is always to fight against the hegemony, and when their signs become appropriated or outdated, the resistant have to find new, unexpected, jarring visual methods of revolt.
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