In line with the latter hypothesis, labeled endothelial cells can be found at higher frequency in solid organs of neonatally tolerized rats injected with hPLAP-tg BMC, 1 week post-injection (R.G. Erben, unpublished results).
To test this hypothesis, CFSE labeled B16F10 and CD45+ cells were detected in blood 24 h after injection of B16F10 cells into the blood of RNF13-KO and WT mice.
To test this hypothesis, we labeled E. muris-infected DH82 cells with carboxyfluorescein succinimidyl ester (CFSE) and seeded the infected cell culture with non-labeled uninfected DH82 cells.
To test this hypothesis, we labeled actin filaments with phalloidin conjugated Quantum dots (Qdots) and/or Alexa 488 Phalloidin, and tracked their movement in and out of the nascent contractile ring.
To test this hypothesis, we labelled primary DG cells with BrdU before transplantation to determine whether cells re-populating the DG were post-mitotic at the time they were transplanted.
As a starting hypothesis, we labeled all the sequences in the gold standard according to our previously proposed classification, based on the presence of key functional residues in the proton conducting channels (Table 1).
To test this hypothesis, we labelled two pools of individual human dynein complexes with different fluorophores and mixed them in the presence of dynactin and BICD2N.
Once again, and in line with our predictions, the two epimeric biotinylated ThrCer analogues behaved differently in their ability to activate iNKT cells, and in accord with our hypothesis, the labeled analogue, possessing the (S -configuration at the tethering S -configurationgnificatthe betethering itsite)-epimer.
The set of the calculated differences is the exact distribution of possible differences under the null hypothesis that group labels do not matter.
Once side of the scales is labeled "Theism" and the other side is labeled "Hypothesis of Indifference".
