human prostate tissue slides (BioChain Institute)
Structured Review

Human Prostate Tissue Slides, supplied by BioChain Institute, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/result/human prostate tissue slides/product/BioChain Institute
Average 90 stars, based on 1 article reviews
Images
1) Product Images from "Macrophages Cytokine Spp1 Increases Growth of Prostate Intraepithelial Neoplasia to Promote Prostate Tumor Progression"
Article Title: Macrophages Cytokine Spp1 Increases Growth of Prostate Intraepithelial Neoplasia to Promote Prostate Tumor Progression
Journal: International Journal of Molecular Sciences
doi: 10.3390/ijms23084247
Figure Legend Snippet: Increased infiltrating macrophages in the prostate intraepithelial neoplasia were M2 subtype. ( A ) Human tissue samples of prostate cancer containing the area of prostate intraepithelial neoplasia (PIN) were immunostained with the antibody of CD68, a pan marker for macrophages (top panel, and middle panel: zoom-in areas). Hematoxylin and eosin (H & E) staining was carried out to visualize the morphology of the prostate cancer tissues (bottom panel). Scale bar: 25 µm. ( B , C ) Raw 264.7 macrophages cultured with either control media or Pr111 PIN complete media were fixed, permeabilized, and immunostained with antibodies for markers of pan macrophages, F4/80; M1 macrophages including iNOS ( B ) and CD38 ( C ); M2 macrophages including Ym1 ( B ) and CD206 ( C ). Scale bar: 20 µm. ( D ) Human tissue samples of PIN were immunostained with antibodies of CD68 and CD206 for the assessment of all macrophages (green) and M2 macrophages (red), respectively. Nuclei were labeled by DAPI and visualized. Scale bar: 50 µm. The image shown here is representative of at least 3 independent experiments or tissue samples.
Techniques Used: Marker, Staining, Cell Culture, Control, Labeling
Figure Legend Snippet: Expression of Spp1 receptors in PIN cells. ( A ) Cell lysates from murine PIN Pr111 cells grown on Matrigel in 3D treated with recombinant Spp1 or control for 72 h were subjected to immunoblotting for assessment of the Spp1 receptors, including integrin αvβ3, integrin β1, and CD44. Long exposure: longer time to catch the emitted signal from the WB membrane on the X-ray film. ( B – E ) Human tissue samples of normal prostate and prostate cancer containing PIN areas were immunostained for the expression of CD44 ( B ), integrin αv ( C ), integrin β1 ( D ), and integrin β3 ( E ). Scale bar: 50 µm. the image shown here is representative of at least 3 independent experiments or tissue samples.
Techniques Used: Expressing, Recombinant, Control, Western Blot, Membrane
Figure Legend Snippet: Macrophage Spp1 activated Akt and JNK signaling in PIN cells. ( A – C ) Pr111 cells cultured on Matrigel in 3D were stimulated with either control/ddH 2 O or recombinant Spp1 for 72 h. Cell lysates were collected and subjected to immunoblotting to examine the proteins of interest, including p-Akt, Akt, p-ERK, and ERK ( A ); p-JNK, JNK, p38 MAPK, p38 MAPK, p-Src, and Src ( B ); and IκBα ( C ). The relative intensity fold change was calculated by the ratio of phosphorylated protein levels over the corresponding total protein levels and set as 1 for the control in each case. Each image shown is representative of 3–5 independent experiments. ( D ) Human tissue samples of normal prostate and prostate cancer containing PIN areas were immunostained for phospho-Akt expression. Scale bar: 25 µm. n = 3.
Techniques Used: Cell Culture, Control, Recombinant, Western Blot, Expressing
