Sentence examples for vector revealed a from inspiring English sources

Flow cytometric analysis of UCB BM cells transduced with a negative control vector revealed a robust engraftment of human nucleated haematopoietic cell (CD45+) in transplanted recipient mice at 16 weeks after transplantation (Fig. 5b).

Nuclear run-on analysis with the CFTR vector revealed a block to transcriptional elongation within the CFTR cDNA.

Unexpectedly, sequence analysis considering the one in frame with the lacZ gene and the adaptor sequence including the EcoRI restriction cloning site (GAATTCGGCACGAG) used to clone the 5'3' cDNA fragments in the λZAP vector revealed a stop codon (TAA in T. solium and E. multilocularis and TGA in the others cestodes) 12 amino acids downstream of the reading frame.

The ANOVA on the length of the mean direction vector revealed an effect of target presence, F 1, 9) = 155, p <.001.

Line-broadening analysis of the intensity distribution along the diffraction vector reveals a 15-times increase in dislocation density in the near-surface zone in the center of the indent.

The distributions of similarity coefficients of feature vectors revealed a clear distinction between high within-subject similarity (i.e. stability), and low between-subject similarity (i.e. variation).

Flow cytometric analysis of UCBs transduced with NAP1L3 shRNA vectors revealed a dramatic increase in the proportion of myeloid cells, compared to UCBs transduced with non-targeting vectors (p-value = 0.0006), and a resulting reverse correlation of non-myeloid cells (Fig. 5d).

Extensive quantitative analysis of an array of vectors revealed a high level of adjustability as well as tight transgene regulation with low levels of leaky expression, both crucial for therapeutical applications.

As shown in Fig.  2a, both vectors revealed a similar fluorescent signal output in transfected live cells showing that the fusion of the reporter did not affect fluorescent emission.

Quantitative PCR of the CMV promoter region of the vectors revealed an up to 63-fold higher yield for the selected capsid variants compared to AAV-2 wild-type vectors and up to 74-fold higher yield compared to random control insert vectors (Figure 5A).

Functional characterization of these new vectors revealed an unexpected position effect that was independent of the identity of the heterologous gene or the transcriptional control element.