Sentence examples for breast tissue sections using from inspiring English sources

Immunohistochemical analysis was performed on paraffin-embedded human breast tissue sections using a peroxidase-antiperoxidase system (DAKO, Carpinteria, CA), as described previously [9].

Immunohistochemistry performed on normal breast tissue sections using monoclonal anti-MTUS1 antibodies revealed a strong cytosolic staining in luminal epithelial cells of the breast (Fig. 1D).

RNA was extracted from slide mounted breast tissue sections using a RNA extraction kit manufactured by Roche to NanoString's specifications [ 26].

To find out if this holds true for CXCL9 as well, we performed immunohistochemical analyses of primary breast cancer tissue sections using a monoclonal antibody to CXCL9.

Breast non-malignant tissue sections used as control showed no staining with the pmCiC antibody (data not shown).

No immunostaining was observed in HNSCC tissue sections used as negative controls where the primary antibody was replaced by isotype specific IgG (Figure 1B (vi)), while the positive control (ER-negative breast cancer) showed S100A7 expression (Figure 1B (vii)).

Positive staining of normal breast epithelial cells that either co-existed on the tumour sections and/or normal breast tissue sections from the same breast was used as a control.

To extend our previous in vitro observations, we analyzed the breast tissue sections of healthy subjects and invasive ductal carcinoma breast patients for the presence of OPG by immunohistochemical staining using anti-OPG antibody.

Low-level-activated c-Src was detected in 12% normal breast tissue sections.

Each FISH assay included normal breast tissue sections, as negative control, and sections of breast cancer previously confirmed to have amplification of EGFR as positive control.

Tonsil sections were used as a positive control for Ki67 staining and breast tissue was used for ER staining.