In some cases, this results from deliberate attempts to translate the vision of designers and marketers into a product that can help consumers express key aspects of their identity.
Analysis of the transcriptional profiles of these LNSC subsets indicated that SCs express key immune mediators and growth factors, and provided important insights into the lymph node conduit network, FRC-specialization, and the DNC identity.
Our findings show that R28 cells express key neuronal markers calbindin, protein kinase C and the microtubule associated protein-2 (MAP-2) by confocal immunofluorescence which has not been shown before, but also calretinin which has not been reported previously.
These results show that embryonic tissues express key circadian genes and have the capacity to express active circadian regulatory cycles.
Subpopulations of neurons located in the ventromedial part of the ARC express key neuropeptides controlling feeding behavior.
However, we have previously shown that undifferentiated SH-SY5Y cells express key dopaminergic markers [27], including the dopamine transporter, and were therefore confident in using these cells for the current study.
As three of the most important fetal organs for growth and development, these tissues express key imprinted genes at high levels [12], [18] and are also representative as sites of tissue-specific expression [19].
Although hESC-CMs are known to exhibit [Ca2+]i transients and express key Ca2+ handling proteins, including SERCA2b, the Na+/Ca2+ exchanger, and RyR2, there has been considerable controversy as to the fundamental mechanisms of excitation-contraction coupling in these cells [43] [46].
Thus it appears that our synaptosomes not only express key proteins involved in plasticity but also display intact synapses containing AMPARs appropriately localized to subcellular compartments poised to carry out the trafficking events associated with LTP and depotentiation.
RT-PCR analyses showed that under standard culture conditions [DMEM (Gibco) + 10% fetal calf serum], the cultured STRO-1+ cells did not express key markers of the osteogenic (cbfa 1, osteocalcin) or chondrogenic (chondroadherin) lineages (Fig. 5a).
