In addition to the validation of previously characterized RPC markers, the single cell method revealed the expression of new genes broadly expressed in RPCs that were not previously characterized in the retina, such as tropomyosin 4 (Tpm4).
Finally, cytokine profiling of an NRAGE over-expressing stable line revealed the expression of macrophage migration inhibitory factor.
Western blot analyses revealed the expression of GNA up to 2.0% of total protein in some of the transgenic plants.
A recent study of Gutroneo et al. (2012) [61] revealed the expression of muscle-specific integrins in masseter muscle fibers during malocclusion disease.
In vitro protein analysis on cell culture supernatant as well as immunohistochemistry of primary and metastatic melanoma tissue revealed the expression of this short form of P-cadherin.
SDS-PAGE analysis revealed the expression of two new proteins of approximately 85 kDa and 79 kDa respectively in arsenic-adapted A. hydrophila.
Immuncytochemical and gene expression analysis revealed the expression of Pax6, Atoh7 and BRN3B increased in 3D fibrin culture compared to 2D conventional culture.
The transcriptome analysis of P. falciparum revealed the expression of ~ 5000 genes, in which ~ 60% of the genes have unknown function.
Reverse transcription-polymerase chain reaction (RT-PCR) and genomic PCR using a pair of gene-specific primers revealed the expression of two alternatively spliced forms of sbGHR in various tissues of the fish.
The antibody revealed the expression of Eag1 in different regions of the rat hippocampus.
Steady-state inactivation protocols in combination with pharmacology revealed the expression of R-type channels.
