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About 10,000 papers for “Staining”

Staining

American Association of Petroleum Geologists eBooks · 1978

Cited by 0

staining

Sawaragi, Eiichi · Figshare · 2022

raw dataHE,AZAN,CD31,CD68,CD163 on day7,14,and 21

Cited by 0Open access

staining

Sawaragi, Eiichi · Figshare · 2022

raw dataHE,AZAN,CD31,CD68,CD163 on day7,14,and 21

Cited by 0Open access

staining

H. Jonas Karlsson, Maja Eriksson, Erik Perzon et al. · 2003

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Staining

American Association of Petroleum Geologists eBooks · 1979

Cited by 0

Staining

Hafsc Phenotype, Karyotype Before Injection · 2013

hAFSC, before injection, present a fibroblastoid shape as shown in Figure 1A. The cells were then tested to confirm a normal karyotype before in vivo applications, to exclude chromosomal abnormalities that could compromise their pluripotential capability (Figure 1B). hAFSC were analyzed for the expression of early and late kidney markers before injection. As shown in Figure 1C, prior to injection, hAFSC were negative for the most important kidney markers, ranging from transcription factors expressed during early kidney development to late differentiation markers. Thus, we confirmed that hAFSC are not specifically committed to kidney progenitor cells when cultured in vitro.

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staining

Pinky A. Bautista, Yukako Yagi · 2016

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staining

2022

(1) In wood finishing, the process of applying coloring matter to the outer surfaces of wood to enhance characteristic grain, provide uniform overall color, or to imitate or match other cabinet woods. (2) Also a textile treatment for the purpose of identifying the fibers present. See Table 4.

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Neuromelanin staining (Fontana-Masson staining)-DAB staining on midbrain organoids v1

michela.deleidi not provided, Maria Jose Perez J., Hariam Raji et al. · 2023

Fontana-Masson staining is a silver staining technique that is commonly used to identify melanin-containing cells. That was combined with DAB-TH staining that works by using an antibody to detect the presence of TH, followed by a reaction with a substrate (DAB) that results in the formation of a brown-colored product at the site of the antigen-antibody interaction.

Cited by 0Open access

Neuromelanin staining (Fontana-Masson staining)+ TH-DAB staining on midbrain organoids v1

Michela Deleidi, Federico Bertoli, Hariam Raji · 2023

Fontana-Masson staining is a silver staining technique that is commonly used to identify melanin-containing cells. We combined it with DAB-TH staining that works by using an antibody to detect the presence of TH, followed by a reaction with a substrate (DAB) that results in the formation of a brown-colored product at the site of the antigen-antibody interaction.

Cited by 0Open access

H&E staining, Safranin O staining and immunohistochemical staining for Col2.

Eva Haltmayer (6541802), Iris Ribitsch (4926154), Simone Gabner (6541805) et al. · Figshare · 2019

<p>Osteochondral explants of control groups (top row) and OA model groups (bottom row) after Hematoxylin and Eosin (H&E) staining, Safranin O staining, and immunohistochemical staining for collagen type-2 (Col2) at week 3. For further analysis, the cartilage explants were divided into three zones (see top left micrograph): superficial zone (s), middle zone (m) and deep zone (d).</p>

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AnnexinV staining.

Lisa Annabel Weber (9606421), Anne Funtan (9606424), Reinhard Paschke (553784) et al. · Figshare · 2020

<p>Percentage of EMM cells (MelDuWi) untreated (control) or treated with BBS and NVX-207 at their double IC<sub>50</sub> concentrations for 48 h.</p> <p>(DOCX)</p>

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Cell staining.

Katelyn Truong (4734837), Suzanne Bradley (4734816), Bryana Baginski (4734825) et al. · Figshare · 2018

<p>After irradiation, control samples (A) and irradiated samples (B) were stained for collagen (red), nuclei (blue), and cells (green) at 10X magnification on Day One after irradiation. Irradiated cells (C) stained to show collagen production.</p>

Cited by 0Open access

AnnexinV staining.

Lisa Annabel Weber (9606421), Anne Funtan (9606424), Reinhard Paschke (553784) et al. · Figshare · 2020

<p>Percentage of equine dermal fibroblasts PriFri2 untreated (control) or treated with BBS and NVX-207 at their double IC<sub>50</sub> concentrations for 48 h.</p> <p>(DOCX)</p>

Cited by 0Open access