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Three bands were identified using this antibody in PNM preparations that migrated at 28, 33 35 and 62 64 kDa.
STAT5 protein bands were identified using human muscle stimulated with GH as positive controls [14].The remaining bands were identified using insulin stimulated rat muscle [16].
Immunoreactive bands were identified using enhanced chemiluminescence according to the manufacturer's instructions.
Labelled bands were identified using enhanced chemo-luminescence (Amersham).
No bands were identified using pooled sera from healthy controls.
Reactive bands were identified using two-dimensional gel electropheresis and MALDI TOF microsequencing.
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Following this, active sub-bands are identified using a constant false-alarm detector, and multiuser detection is achieved using a bandwidth constraint.
A "faint band" was identified using the same definition as Kyabayinze et al. (2008), where "faint bands" are those that are only visible in good light.
Western blot analyses revealed specific bands that were identified using CB2 antibodies and were absent when the CB2 antibodies were pre-adsorbed with the immunizing peptide [24].
For testing the assembly reliability of the physical map, 96 clones representing 14 randomly selected contigs with a size ranging from 269 to 1099 consensus band (CB) units were identified using the minimum tiling path (MTP) method for BAC end sequencing (BES; Table 3).
The other major lipid class bands from TLC plates, were identified using commercial standards (which were run in parallel with the samples) and then scraped from the plates.
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