Sentence examples for models were stained from inspiring English sources

The typodont models were stained with a water-based colour and brushed for 1 minute.

Tissue sections from human skin and the skin equivalent models were stained in the same manner.

All comb models were stained for 15 minutes with 1% crystal violet [ 6], based on the methods of Pitts et al. [ 19] and Stepanovic et al. [ 23].

Cryosections of tissue models were stained as described (Nguyen Hoang et al., 2012) with polyclonal rabbit HMGB-1 (Abcam, Cambridge, UK) overnight at room temperature followed by biotinylated anti-rabbit secondary Ab (Dako, Glostrup, Denmark).

Formalin-fixed, paraffin-embedded sections of primary tumour and/or metastatic tissues from patients with OS and from mouse cancer models were stained with haematoxylin and eosin for morphological evaluation.

Cryosections (8 μm) of the tissue models were stained as described (Nguyen Hoang et al., 2012) with anti-human CD68 (Dako, Glostrup, Denmark) overnight at room temperature followed by a biotinylated anti-mouse antibody (Ab; Dako, Glostrup, Denmark).

To determine the contribution of macrophages, the dominant cell type involved in cartilage destruction within this model, sections were stained with antibodies directed against F4/80.

In order to validate our findings from mouse models, human TMAs were stained for expression of PTEN and were scored independently by two pathologists on a scale of 0 (no staining) to 2 (intense staining).

To visualize the DCIS lumen model, MCF10a cells were stained with green cell tracker dye (10 μM, Life Technologies, Grand Island, NY, USA) and MCF10aDCIS cells were stained with blue cell tracker dye (10 μM, Life Technologies, Grand Island, NY, USA) for 30 minutes prior to each respective cell seeding.

Tissue slices obtained from animal models or surgical biopsies were stained ex vivo in Tyrode's buffer containing 1% BSA at 37°C containing 4 nm QD-EGF or QD-MAb for 30 min with gentle agitation followed by 3 changes of Tyrode's/BSA for 15 min or 30 min of 10 mg/ml MAb followed by washing and subsequent staining with 10 nM QD-GAMIG and washing.

For detection of DCs present in the lymph nodes and presentation of the model tumor antigen, the cells were stained with CD11c-FITC (BD Pharmingen), CD8-APC (BD Pharmingen), OVA257-264 (SIINFEKL -PE (eBioscience) and CD3-V450 (BD Pharmingen).