Slides with 5-µM sections from the paraffin-embedded specimens were deparaffinized and rehydrated. ❋ Jeran K. Stratford Et Al. (2010)
Fluorescence in situ hybridization (FISH) was performed on deparaffinized formalin fixed sections using a eubacterial probe (EUB3380Cy3) and antisense control probe (nonEUB338-FAM), and visualized on an Olympus BX-51 fluorescense microscope and DP70 camera as previously described Primary endometrial epithelial and stromal cells were isolated and cultured as described previously ❋ I. Martin Sheldon Et Al. (2010)
Tissue sections were deparaffinized in citrosolv and rehydrated through graded concentrations of ethanol to 0.1 M Tris buffered saline (TBS, pH 7.6). ❋ Lori C. Albergotti Et Al. (2009)
Briefly, the TMA section was deparaffinized, rehydrated, and submitted to heat antigen retrieval in an ethylenediamine tetra acetic acid buffer ❋ Unknown (2009)
Paraffin fixed sections of the placenta were sectioned at 2 µm thickness, then deparaffinized and rehydrated. ❋ Karen May Et Al. (2009)
The paraffin sections were deparaffinized and pretreated in 10 Mm citrate buffer (ph 6) in microwave oven for 20 minutes. ❋ Deepti Joshi Et Al. (2009)
For immunohistochemical studies the sections were deparaffinized and rehydrated. ❋ Unknown (2009)
Tissue sections were routinely deparaffinized and rehydrated through graded alcohols and incubated overnight at room temperature with a biotinylated monoclonal BrdU antibody (Zymed, South Francisco, CA). ❋ Payel Bhanja Et Al. (2009)
Paraffin-embedded tissue sections (6µm) were mounted onto positively charged glass slides, deparaffinized, and rehydrated through graded ethanol. ❋ Nicholas J. Haley Et Al. (2009)
Immunofluorescence stainings were carried out according to the following basic protocol: Paraffin embedded sections were deparaffinized and rehydrated. ❋ Unknown (2009)
These areas were subsequently macrodissected with a scalpel from thick (10 um) deparaffinized sections and brought into 1.5 ml tubes for tissue digestion. ❋ Vassiliki Kotoula Et Al. (2009)
The sections were air-dried, deparaffinized in xylene, and rehydrated in a graded ethanol series. ❋ Kristiina Kanerva Et Al. (2009)
Paraffin-embedded sections were deparaffinized, rehydrated and subsequently blocked with 10\% normal goat sera containing 0. 1\% BSA and 0. 2\% glycine. ❋ Zhihong Wu Et Al. (2009)
For immunohistochemical stainings sections were deparaffinized and rehydrated. ❋ Unknown (2009)
For Prussian blue staining, slide mounted sections were deparaffinized, rehydrated, and reacted for 30 minutes in 2\% potassium ferrocyanide and 3. 7\% hydrochloric acid to visualize ferric iron particles by Prussian blue. ❋ Arnaud Beduneau Et Al. (2009)
Histology was done on formalin-fixed, paraffin-embedded lung specimen. 6 µm-cut sections were deparaffinized, rehydrated in graded alcohols and haematoxylin-eosin (H&E) stained. ❋ Unknown (2009)
Sections were deparaffinized, rehydrated through a graded series of ethanols, and washed in water. ❋ Andrzej Swistowski Et Al. (2009)
Streck-fixed, paraffin-embedded brain tissue sections were deparaffinized, rehydrated, and then post-fixed in Streck tissue fixative ❋ Joseph L. Mankowski Et Al. (2008)
For human fetal pancreases, 4 µm-thick sections were cut on gelatinized glass slides, deparaffinized in toluene, and rehydrated. ❋ Unknown (2008)