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The cellular behaviors that generate bands are unknown.
Both SUMO-1 and anti-HA abs generate bands migrating in corresponding positions of the gel, at a molecular weight higher than monomeric Tollip (compare lanes 3 and 5).
The ChpPV P7 probe, which spans the putative A1-1 acceptor, was protected to generate bands of 240 nts and 153 nts (Fig. 2B, lane 8), which represent RNAs that are unspliced and spliced at the A1-1 site, respectively.
Wild type chromosomes generate a band of 3 kb, whereas deletions generate bands of ~490 bp.
These primers were chosen from regions that are conserved between the serotype A and D genomes and following PCR can generate bands of distinct size from serotype A and D strains.
In the simplest protocols, which used just 1 set of primers, the Hp allele and the Hp allele were amplified to generate bands of 1757 bp and 3481 bp, respectively (protocol 1).
Similar(53)
Here, the combination of P1/P2 primer could not generate band in MYB10.1-2/MYB10.1-2 topes due thethe long size (over 5800 bp) of amplicon.
The amplification of these DNA sequences generated bands of 500 600 pair of bases (pb) for ITS, and 1100 pb for DNAr 28S.
In addition, all antibodies used generated bands at the predicted molecular weight.
We assume that the number of the generated bands corresponds to that of goat and sheep V1R genes in each subfamily.
Amplification of cDNA generated bands of expected sizes, representing the expression of the CRH, CRHR1, CRHR2 and FasL genes, with the exception of CRHR2, which was not expressed in OvCa3 cells.
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