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In-gel digestion of individual protein bands was carried out utilizing a procedure described in http://msf.ucsf.edu/ingel.html.html
In-gel digestions on Pil1 bands were carried out utilizing a procedure described at http://msf.ucsf.edu/ingel.html.html
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At several loading stages after cracking, the values of α are calculated at the mid-shear span of each beam utilizing the procedure described in previous section, and the results are summarized in Fig. 12.
The prepared non-glycosylated apo- and hololactoferrin samples were loaded separately into a 50-μl loop, injected into the MonoS column, and chromatographic separation was performed by utilizing the procedure described above.
We thus utilize the forward-selection procedure, described above, to determine which of the first three axes of genetic variation are correlated with phenotype.
After an evaluation procedure described in Sect.
The procedure described here utilizes native-space morphometry as well as a method for dividing the insula into connectivity-based sub-regions estimated from cytoarchitectonics.
The authors utilized a previously described cadaver model [ 22].
Genotyping initially utilized additional polymorphic microsatellite markers, following the procedure described above, and sequencing of known polymorphic SNPs identified from the Mouse Phenome Database (www.jax.org/phenome).org/phenome
The same Sobel procedure described above was utilized to assess mediation of NA-stimuli in the relationship between group (CSA, NSA) and Arousal-function and Satisfaction (DVs).
The procedure described above for the isolation of short nascent DNA was utilized on a culture of exponentially growing MCF-7 cells.
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