hematoxylin bluing solution Search Results


86
Servicebio Inc hematoxylin bluing solution
Hematoxylin Bluing Solution, supplied by Servicebio Inc, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hematoxylin+bluing+solution/differentiation+hematoxylin+solution/pm41097289-163-14-17
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99
Beyotime hematoxylin staining
miR-382 inhibits the metastasis of 4T1 breast cancer cells by inhibiting the polarization of M2 macrophages in vivo . (A and B) Mouse macrophages transfected with miR-382-overexpressing lentivirus were mixed with 4T1 cells at a 4:1 ratio and subcutaneously inoculated into BALB/c mice, and breast tumor growth was monitored. The long and short diameters of the tumors were measured every 5 days, and the tumor volume was calculated using the formula ab 2 /2. the maximum diameter of tumors did not exceed 2 cm. (C and D) After observation, the mice were sacrificed, lung tissues were harvested for <t>hematoxylin</t> and eosin staining, the tumor growth rate was determined, and the number of metastases was calculated. Images were captured under 400× magnification. (E and F) At the end of the experiment, the mice were sacrificed, tumor tissues were harvested and embedded in paraffin, and immunohistochemical staining was performed. Images were captured under ×400 magnification. Data are presented as the mean ± SD of three independent experiments ( ** P<0.01).
Hematoxylin Staining, supplied by Beyotime, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/hematoxylin+bluing+solution/Hematoxylin+Staining+Solution/pmc09477106-123-23-67
Average 99 stars, based on 1 article reviews
hematoxylin staining - by Bioz Stars, 2026-10
99/100 stars
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90
Gilford Instrument Laboratories Inc model 250 spectrophotometer
miR-382 inhibits the metastasis of 4T1 breast cancer cells by inhibiting the polarization of M2 macrophages in vivo . (A and B) Mouse macrophages transfected with miR-382-overexpressing lentivirus were mixed with 4T1 cells at a 4:1 ratio and subcutaneously inoculated into BALB/c mice, and breast tumor growth was monitored. The long and short diameters of the tumors were measured every 5 days, and the tumor volume was calculated using the formula ab 2 /2. the maximum diameter of tumors did not exceed 2 cm. (C and D) After observation, the mice were sacrificed, lung tissues were harvested for <t>hematoxylin</t> and eosin staining, the tumor growth rate was determined, and the number of metastases was calculated. Images were captured under 400× magnification. (E and F) At the end of the experiment, the mice were sacrificed, tumor tissues were harvested and embedded in paraffin, and immunohistochemical staining was performed. Images were captured under ×400 magnification. Data are presented as the mean ± SD of three independent experiments ( ** P<0.01).
Model 250 Spectrophotometer, supplied by Gilford Instrument Laboratories Inc, 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/product/hematoxylin+bluing+solution/spectrophotometer+model+250/pm00516005-85-27-30
Average 90 stars, based on 1 article reviews
model 250 spectrophotometer - by Bioz Stars, 2026-10
90/100 stars
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Image Search Results


miR-382 inhibits the metastasis of 4T1 breast cancer cells by inhibiting the polarization of M2 macrophages in vivo . (A and B) Mouse macrophages transfected with miR-382-overexpressing lentivirus were mixed with 4T1 cells at a 4:1 ratio and subcutaneously inoculated into BALB/c mice, and breast tumor growth was monitored. The long and short diameters of the tumors were measured every 5 days, and the tumor volume was calculated using the formula ab 2 /2. the maximum diameter of tumors did not exceed 2 cm. (C and D) After observation, the mice were sacrificed, lung tissues were harvested for hematoxylin and eosin staining, the tumor growth rate was determined, and the number of metastases was calculated. Images were captured under 400× magnification. (E and F) At the end of the experiment, the mice were sacrificed, tumor tissues were harvested and embedded in paraffin, and immunohistochemical staining was performed. Images were captured under ×400 magnification. Data are presented as the mean ± SD of three independent experiments ( ** P<0.01).

Journal: International Journal of Oncology

Article Title: miR-382 inhibits breast cancer progression and metastasis by affecting the M2 polarization of tumor-associated macrophages by targeting PGC-1α

doi: 10.3892/ijo.2022.5416

Figure Lengend Snippet: miR-382 inhibits the metastasis of 4T1 breast cancer cells by inhibiting the polarization of M2 macrophages in vivo . (A and B) Mouse macrophages transfected with miR-382-overexpressing lentivirus were mixed with 4T1 cells at a 4:1 ratio and subcutaneously inoculated into BALB/c mice, and breast tumor growth was monitored. The long and short diameters of the tumors were measured every 5 days, and the tumor volume was calculated using the formula ab 2 /2. the maximum diameter of tumors did not exceed 2 cm. (C and D) After observation, the mice were sacrificed, lung tissues were harvested for hematoxylin and eosin staining, the tumor growth rate was determined, and the number of metastases was calculated. Images were captured under 400× magnification. (E and F) At the end of the experiment, the mice were sacrificed, tumor tissues were harvested and embedded in paraffin, and immunohistochemical staining was performed. Images were captured under ×400 magnification. Data are presented as the mean ± SD of three independent experiments ( ** P<0.01).

Article Snippet: Tumors derived from 4T1 cells and lung tissues were removed and fixed in 4% paraformaldehyde (BL539A, Biosharp) for 24 h. Following tissue dewaxing, hematoxylin staining (hematoxylin was added to the sections, incubated for 4 min at room temperature, differentiated with 0.5% hydrochloric acid alcohol for 20 min, re-blued with 0.5% ammonia for 30 sec, stained with eosin dye by drop for 1 min, at a constant temperature; Beyotime Institute of Biotechnology Co., Ltd.), dehydration and clearing (washed with 80% ethanol for 10 sec, 95% ethanol for 10 sec, absolute ethanol for 5 min, absolute ethanol for 10 min, and xylene for twice, 10 min for each time.

Techniques: In Vivo, Transfection, Staining, Immunohistochemical staining