Stem Cell Marker Sox2

Sox2 is a transcription factor and stem cell marker that helps identify and regulate cells with self-renewal or developmental potential, making it important for studying tissue formation and cell fate. It functions by binding regulatory DNA sequences and working with other factors, including Oct4, to control gene networks that maintain stemness while influencing differentiation. In developmental biology, Sox2 expression is used to examine early embryonic development, neural progenitor populations, and the transition between undifferentiated and specialized cell states. Its detection supports research on organ formation, regeneration, and diseases involving abnormal cell identity or growth.

Stem Cell Marker Sox2 - Related Videos

Research

JoVE Journal - Biology

Derivation of Hematopoietic Stem Cells from Murine Embryonic Stem Cells

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Cited by 7 •

2007

This protocol details the derivation of transplantable hematopoietic stem cells from mouse embryonic stem cells (ESC) and their subsequent injection into lethally irradiated recipient mice. Briefly, ESC are differentiated as embryoid bodies, which are then infected with retroviral HoxB4 and co-cultured with OP9 stromal cells and hematopoietic cytokines.

Research

JoVE Journal - Neuroscience
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Enumeration of Neural Stem Cells Using Clonal Assays

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Cited by 5 •

2016

Neural stem cells (NSCs) refer to cells which can self-renew and differentiate into the three neural lineages. Here, we describe a protocol to determine NSC frequency in a given cell population using neurosphere formation and differentiation under clonal conditions.

A Quick and Efficient Method for the Purification of Endoderm Cells Generated from Human Embryonic Stem Cells

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Cited by 6 •

2016

Here, we describe a method for the purification of differentiated human embryonic stem cells that are committed towards the definitive endoderm for the improvement of downstream applications and further differentiations.

Identifying Cell Surface Markers of Primary Neural Stem and Progenitor Cells by Metabolic Labeling of Sialoglycan

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Cited by 1 •

2019

Presented here is a protocol that combines an in vitro neural-endothelial co-culture system and metabolic incorporation of sialoglycan with bioorthogonal functional groups to expand primary neural stem and progenitor cells and label their surface sialoglycoproteins for imaging or mass-spectrometry analysis of cell surface markers.

Development, Expansion, and In vivo Monitoring of Human NK Cells from Human Embryonic Stem Cells (hESCs) and Induced Pluripotent Stem Cells (iPSCs)

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Cited by 45 •

2013

This protocol describes the development, expansion, and in vivo imaging of NK cells derived from hESCs and iPSCs.

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