In situ DNA TRANSFER TO CHICKEN EMBRYOS BY BIOLISTICS

Primarily, the tumor suppressor gene expression was assigned to genes involved in the control of strategic points of the chain of events related to cell growth and

Fold change in mRNA expression in adipocytes was normalized to input of cDNA (n=γ) (B) Cells were differentiated for 1β days in the absence or presence of β00 µM UDCA or 500 µM

The percentage of embryos with at least one blue focus (% of GUS+) and the number of blue foci per embryo were recorded, and the re- generation frequency (percentage of immature

(A) Single cell suspensions of the indicated cell populations or tissues were analyzed by flow cytometry for RON expression using a monoclonal antibody specific for murine RON

To investigate the effects of Scriptaid treatment on mRNA and protein expression during early embryonic development, the expression levels of development-related genes and proteins

TC620 cells were transfected with luciferase reporter plasmid for the early promoter, JCV E -LUC in the presence or absence of increasing amounts of Rad51 expression plasmid (0, 0.5

In situ hybridization clarified that the expression patterns of mylz2 , smyhc1 , and mck in Smyd3 morphants were indistinguishable from control embryos injected with Smyd3-mis-MO

Cells grown in both the media demonstrated a similar expression of endothelial cell markers when assessed by immunohistochemistry, although HCEC marker gene expression was higher