<p>AO is a vital dye and stains both live and dead cells. EB penetrates into cells with disrupted cytoplasmic membrane, staining only dead cells. Therefore, viable cells appear uniformly green and dead cells are labelled in orange. a) Low sensitivity (cell mortality 5%). b) Average sensitivity (cell mortality 40%). c) High sensitivity (cell mortality 80%).</p
<p>Detection of apoptosis, necrosis and quantitative changes in dual stained (AO/EB) fluorescence im...
<p>(A) Whole-embryo cell death images were detected by fluorescence microscope. a-1,a-2, Control gro...
BACKGROUND: Photodynamic therapy combines the effects of a chemical agent with the physical energy f...
Cellular injury and death are ubiquitous features of disease, yet tools to detect them are limited a...
Cytotoxicity and cell viability assessments are very important parameters that are widely used in fu...
<p>a and b) HepG2 control cells. c and d) HepG2 cells treated with 25 µg/ml of CD-3. e and f) HepG2 ...
<p>Cells were untreated (A) or treated for 3 h with 1 μM staurosporine (B), 10 μM β-hederin (C), 5 μ...
Source of support: Departmental sources Background: The aim of this study was to evaluate the abilit...
In vitro cell viability tests are usually done using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethox...
The reliability of eight distinct methods (Giemsa staining, trypan blue exclusion, acridine orange/e...
Abstract Background Analyzing apoptosis has been an integral component of many biological studies. H...
<p>Propidium iodide (PI) labels cells lacking intact plasma membranes and hence at an advanced stage...
<p>[A] Untreated and treated-CAOV-3 cells with pulchrin A at 24, 48 and 72 h of treatment. The CAOV-...
Identifying and characterizing different forms of cell death can be facilitated by staining internal...
<p>Detection of apoptosis, necrosis and quantitative changes in dual stained (AO/EB) fluorescence im...
<p>Detection of apoptosis, necrosis and quantitative changes in dual stained (AO/EB) fluorescence im...
<p>(A) Whole-embryo cell death images were detected by fluorescence microscope. a-1,a-2, Control gro...
BACKGROUND: Photodynamic therapy combines the effects of a chemical agent with the physical energy f...
Cellular injury and death are ubiquitous features of disease, yet tools to detect them are limited a...
Cytotoxicity and cell viability assessments are very important parameters that are widely used in fu...
<p>a and b) HepG2 control cells. c and d) HepG2 cells treated with 25 µg/ml of CD-3. e and f) HepG2 ...
<p>Cells were untreated (A) or treated for 3 h with 1 μM staurosporine (B), 10 μM β-hederin (C), 5 μ...
Source of support: Departmental sources Background: The aim of this study was to evaluate the abilit...
In vitro cell viability tests are usually done using 3-(4,5-dimethylthiazol-2-yl)-5-(3-carboxymethox...
The reliability of eight distinct methods (Giemsa staining, trypan blue exclusion, acridine orange/e...
Abstract Background Analyzing apoptosis has been an integral component of many biological studies. H...
<p>Propidium iodide (PI) labels cells lacking intact plasma membranes and hence at an advanced stage...
<p>[A] Untreated and treated-CAOV-3 cells with pulchrin A at 24, 48 and 72 h of treatment. The CAOV-...
Identifying and characterizing different forms of cell death can be facilitated by staining internal...
<p>Detection of apoptosis, necrosis and quantitative changes in dual stained (AO/EB) fluorescence im...
<p>Detection of apoptosis, necrosis and quantitative changes in dual stained (AO/EB) fluorescence im...
<p>(A) Whole-embryo cell death images were detected by fluorescence microscope. a-1,a-2, Control gro...
BACKGROUND: Photodynamic therapy combines the effects of a chemical agent with the physical energy f...