Sentence examples for input extracts from inspiring English sources
Kim et al.'s study [7] accepts MPEG-4 video as input, extracts the background Video Object Plane (VOP) and the primary (foreground) VOP, classifies the background motion type (left motion, right motion, or static) according to its MV field, and finally assigns disparities for the foreground and the background VOPs individually.
Similar amounts of GFP and GAPDH proteins were detected in the input extracts (Fig. 3B).
Analysis was completed for each mRNA in the pulldown as compared to the levels in control total input extracts.
As a control, RNA was prepared from the input extracts that were incubated without IgG beads for the same amount of time as the experimental samples that were bound to the IgG beads.
WB of the input extracts and IP proteins (Fig. 3B) revealed that GFP was specifically co-IP from the cytoplasmic extracts of cells infected with EPEC/pT3sVgfp demonstrating the formation of intracellular GFP-T3sVgfp complexes.
Input extracts (2%) and RAD23B-bound proteins were analyzed by western blotting.
If the extracted nouns and noun phrases are not stored in Data Storage, QGS starts Step 4. Step 4: input extracted nouns and noun phrases into the WordNet database, QGS then extracts all matching hyponyms and example sentences.
An image-derived arterial input extracted from scan data using a volume of interest (VOI) placed in the abdominal aorta [14] (median volume 2.18 mL blood; range, 3.4 4.2 mL blood) was used in the day-to-day study and arterial tracer concentrations measured in blood samples were used in the analysis of a correlation between SUV and K met.
Since T3sVamy does not accumulate at detectable levels in the cytoplasm of HeLa cells (likely caused by the absence of its antigen in the cytoplasm; see Discussion), purified T3sVamy was added to the input extract of cells infected with EPEC/pT3sVamy to provide a control of the specific co-IP of GFP with T3sVgfp (Fig. 3B).
For the RNA purified from the input extract, additional purification using the RNeasy MinElute kit (QIAGEN) was carried out.
Samples were sonicated to solubilize kinetochore proteins (12 s, 3 times with 1 min interval on ice), producing "input" extract samples.
