Sentence examples for our immunoblots indicating from inspiring English sources

We observed that none of the tested lichen secondary metabolites affected PrP levels in our immunoblots indicating that they neither degraded PrPTSE nor caused interference with the assay.

The LMP1 gene product could not be detected directly in immunoblots indicating that its expression level was very low (data not shown).

Signal intensities for MCM subunits in CHO and 3T3 lysates were nearly identical to those obtained with human cells in almost all of the immunoblots, indicating that all three mammalian types contain very similar quantities of MCM subunits.

These preparations are negative for porin in immunoblots, indicating that mitochondrial contamination (common in chromosome preparations) is low.

Our immunoblots also indicate that RTN1A associates with RTN4A, as rabbit anti-RTN1A antibodies co-precipitated RTN4A (Fig. 2B, lane 2).

Immunoblots indicate that BHK-21 cell-derived virions shed the GAG binding domain from at least 50% of their gp70 [2].

Quantitative evaluation of the immunoblots indicated that in the presence of NH4Cl the amount of α-synuclein was enhanced supporting the notion that the lysosomal pathway is involved in its degradation (Fig. 4D).

White lines separating lanes in some immunoblots indicate removal of portions of the blots for clarity and/or splicing together of distinct blots.

The autoantibodies were readily detected by RIP, but not by immunoblotting indicating that, like anti-GAD65, they reacted with conformational epitopes.

As shown in Figure 3 (lane 4), MG-132 treatment rendered the LF-cleaved COOH-terminus of MKK4 recognizable by V5 antibody in the immunoblotting, indicating that after LF cleavage MKK4 is degraded through a proteosome-dependent pathway.

However, when treated with N-glycanase (PNGase F), no shift in the apparent molecular weight of secreted Otolin was observed on immunoblot, indicating the absence of N-linked glycans (Fig. 7B).