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©The Author(s) 2023.
World J Stem Cells. Jun 26, 2023; 15(6): 607-616
Published online Jun 26, 2023. doi: 10.4252/wjsc.v15.i6.607
Published online Jun 26, 2023. doi: 10.4252/wjsc.v15.i6.607
Figure 1 Development of neural stem cells derived from newborn rats (inverted phase-contrast microscope).
A: At 24 h after the primary culture (100×); B: 3 d after the primary culture (100×); C: 5 d after the primary culture (100×); D: 8 d after the primary culture (100×); E: 4 d after 5 passages (×200); F: 5 d after induction of dissociation (×200).
Figure 2 Immunofluorescence staining.
A: BrdU immunofluorescence staining (green fluorescence, ×100); B: Nestin immunofluorescence staining (red fluorescence, ×100); C: NF200 + DAPI immunofluorescence staining (green fluorescence refers to NF200, blue fluorescence refers to DAPI, ×200); D: NSE + DAPI immunofluorescence staining (green fluorescence refers to NSE, blue fluorescence refers to DAPI, ×200); E: GFAP + DAPI immunofluorescence staining (green fluorescence refers to GFAP, blue fluorescence refers to DAPI, ×200).
- Citation: Zhou QZ, Feng XL, Jia XF, Mohd Nor NHB, Harun MHB, Feng DX, Wan Sulaiman WA. Culture and identification of neonatal rat brain-derived neural stem cells. World J Stem Cells 2023; 15(6): 607-616
- URL: https://www.wjgnet.com/1948-0210/full/v15/i6/607.htm
- DOI: https://dx.doi.org/10.4252/wjsc.v15.i6.607