2011
DOI: 10.1007/s11626-011-9420-9
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Abstract: Human embryonic stem (hES) cells possess the ability to self-renew indefinitely and provide a potential source of differentiated progeny representing all three embryonic germ layers. Although hES cell lines share the expression of typical pluripotency markers, limited data is available regarding their differentiation capabilities. We have earlier reported the in-house derivation of two hES cell lines, KIND-1 and KIND-2 on human feeders. Here, we describe a comparative study carried out on both these cell lines… Show more

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Cited by 14 publications
(13 citation statements)
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“…Upregulation of some endodermal genes, namely, FLT1, FOXA2 and GATA4 was observed in KIND-1 cells propagated in I-HFF-CM from group I when compared to positive control, but the difference was not significant between groups I and III in respect to positive control. This could be explained by the propensity of KIND-1 cells toward endodermal lineage33. Specific staining for ectodermal marker Tuj1was also confirmed by considering primary control (data not shown).…”
Section: Discussionmentioning
confidence: 71%
“…Upregulation of some endodermal genes, namely, FLT1, FOXA2 and GATA4 was observed in KIND-1 cells propagated in I-HFF-CM from group I when compared to positive control, but the difference was not significant between groups I and III in respect to positive control. This could be explained by the propensity of KIND-1 cells toward endodermal lineage33. Specific staining for ectodermal marker Tuj1was also confirmed by considering primary control (data not shown).…”
Section: Discussionmentioning
confidence: 71%
“…For spontaneous differentiation, embryoid bodies (EBs) were generated from KIND1 cells as described earlier [38]. Three representative genes MAP2 (ectoderm lineage), HAND1 (mesoderm lineage) and MIXL (endoderm lineage) were studied by qRT-PCR from embryoid bodies harvested on day 7 and day 15.…”
Section: Resultsmentioning
confidence: 99%
“…For all the genes, the cycling parameters for PCR comprised of initial denaturation at 94°C for 3 min, followed by 35 cycles of denaturation at 94°C for 30 sec, primer annealing at 62°C for 30 sec and extension at 72°C for 1 min using Dream Taq Polymerase as per manufacturer’s instructions (Thermo Scientific, IL, USA). The primers used for RT-PCR are as described earlier [38]. The PCR products were visualized by electrophoresis on 2% agarose gel, containing 0.5 μg/ml ethidium bromide (Bangalore Genei, Bangalore, India) and the product size was approximated using 100-bp DNA ladder (Bangalore Genei).…”
Section: Methodsmentioning
confidence: 99%
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