<p>Cells were assessed for cell viability at each passage, performed at 90% confluence. Trypan blue exclusion assay differentiated between viable and non-viable cells based upon membrane permeability and growth rate calculated as population doubling per day (A). Growth rate is represented graphically as population doubling over days in culture (B). Phase contrast images at 20x magnification demonstrate morphology of primary passage 3 and 10 HEKn cultured in CnT-07 alone and passage 3 and 10 HEKn-CaY supplemented with Y-27632 (C). n = 3 isolations from separate donors. Data is expressed as Mean +/- SEM. Images are representative of three experimental repeats.</p
10.1002/jbm.a.31864Journal of Biomedical Materials Research - Part A881184-194JBMR
Skin biopsies are a valuable technique in the diagnosis of cutaneous inflammatory and neoplastic con...
Epidermal cell models are critical for studying skin biology. The gold standard used by the scientif...
Human keratinocytes are difficult to isolate and have a limited lifespan. Traditionally, immortalise...
Studies using cultured cells allow one to dissect complex cellular mechanisms in greater detail than...
<p>(<b>A</b>) SNAP-SUMO3 HaCaT cells were plated and induced to differentiate with 2.38 mM calcium. ...
<p>Expression of markers of keratinocyte differentiation in human skin, HaCaT cell line, human Norma...
<p>Keratinocytes and fibroblasts were respectively stained with PHK26 and PHK2 before co-culture. Ke...
Human newborn foreskin keratinocytes were maintained in culture in first passage for up to 60 days. ...
<p>3×10<sup>5</sup> fibroblasts, stained with PHK2 (green), were cultured in 6-well pre-coated plate...
<p>The growth of keratocytes under SMG (A–D): the cellular aggregation in a pore of the carrier (A);...
In vitro aging models are based on the observation that normal cells in culture have a finite lifesp...
Human newborn foreskin keratinocytes were maintained in culture in first passage for up to 60 days. ...
In vitro aging models are based on the observation that normal cells in culture have a finite lifesp...
The RTE cell line is a keratinocyte line derived from explant cultures of stratified squamous epithe...
10.1002/jbm.a.31864Journal of Biomedical Materials Research - Part A881184-194JBMR
Skin biopsies are a valuable technique in the diagnosis of cutaneous inflammatory and neoplastic con...
Epidermal cell models are critical for studying skin biology. The gold standard used by the scientif...
Human keratinocytes are difficult to isolate and have a limited lifespan. Traditionally, immortalise...
Studies using cultured cells allow one to dissect complex cellular mechanisms in greater detail than...
<p>(<b>A</b>) SNAP-SUMO3 HaCaT cells were plated and induced to differentiate with 2.38 mM calcium. ...
<p>Expression of markers of keratinocyte differentiation in human skin, HaCaT cell line, human Norma...
<p>Keratinocytes and fibroblasts were respectively stained with PHK26 and PHK2 before co-culture. Ke...
Human newborn foreskin keratinocytes were maintained in culture in first passage for up to 60 days. ...
<p>3×10<sup>5</sup> fibroblasts, stained with PHK2 (green), were cultured in 6-well pre-coated plate...
<p>The growth of keratocytes under SMG (A–D): the cellular aggregation in a pore of the carrier (A);...
In vitro aging models are based on the observation that normal cells in culture have a finite lifesp...
Human newborn foreskin keratinocytes were maintained in culture in first passage for up to 60 days. ...
In vitro aging models are based on the observation that normal cells in culture have a finite lifesp...
The RTE cell line is a keratinocyte line derived from explant cultures of stratified squamous epithe...
10.1002/jbm.a.31864Journal of Biomedical Materials Research - Part A881184-194JBMR
Skin biopsies are a valuable technique in the diagnosis of cutaneous inflammatory and neoplastic con...
Epidermal cell models are critical for studying skin biology. The gold standard used by the scientif...