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Image Search Results
Journal: Neural Plasticity
Article Title: Transplantation of Neural Stem Cells Cotreated with Thyroid Hormone and GDNF Gene Induces Neuroprotection in Rats of Chronic Experimental Allergic Encephalomyelitis
doi: 10.1155/2016/3081939
Figure Lengend Snippet: Immunohistochemical double staining of BrdU, MAP2, GFAP, and GalC positive cells in the cerebral parenchyma of rats. (a–c) MAP2 − /BrdU + cells (solid arrow), MAP2 + /BrdU − cells (dotted arrow), and MAP2 + /BrdU + cells (arrowhead) in NSCs, T3/NSCs, and GDNF-T3/NSCs group, respectively. (d–f) GalC − /BrdU + positive cells (solid arrow), GalC + /BrdU − cells (dotted arrow), and GalC + /BrdU + cells (arrowhead) in NSCs, T3/NSCs, and GDNF-T3/NSCs group, respectively. (g–i) GFAP − /BrdU + cells (solid arrow), GFAP + /BrdU − cells (dotted arrow), and GFAP + /BrdU + cells (arrowhead) in NSCs, T3/NSCs, and GDNF-T3/NSCs group, respectively. (j) GFAP + cells (dotted arrow) in control group. (k) GFAP + cells (dotted arrow) in normal group. Bar (a–k) = 25 μ m.
Article Snippet: After a goat anti-mouse IgG secondary antibody (1 : 100; Wuhan Boster Biological Technology, China) was added for 30 minutes, alkaline phosphatase- (AP-) streptavidin (Boster) was incubated for 30 minutes, and 5-bromo-4-chloro-3-indolyl phosphate/nitroblue tetrazolium chloride (BCIP/NBT, Boster) was then used as a chromogen for 10 min. After PBS washes, the sections were reincubated with primary antibody for
Techniques: Immunohistochemical staining, Double Staining, Control
Journal: Neural Plasticity
Article Title: Transplantation of Neural Stem Cells Cotreated with Thyroid Hormone and GDNF Gene Induces Neuroprotection in Rats of Chronic Experimental Allergic Encephalomyelitis
doi: 10.1155/2016/3081939
Figure Lengend Snippet: Differentiation of NSCs, T3/NSCs, and GDNF-T3/NSCs in vivo (mean ± SD, n = 5).
Article Snippet: After a goat anti-mouse IgG secondary antibody (1 : 100; Wuhan Boster Biological Technology, China) was added for 30 minutes, alkaline phosphatase- (AP-) streptavidin (Boster) was incubated for 30 minutes, and 5-bromo-4-chloro-3-indolyl phosphate/nitroblue tetrazolium chloride (BCIP/NBT, Boster) was then used as a chromogen for 10 min. After PBS washes, the sections were reincubated with primary antibody for
Techniques: In Vivo
Journal: Cell
Article Title: Neuromodulator Signaling Bidirectionally Controls Vesicle Numbers in Human Synapses
doi: 10.1016/j.cell.2019.09.011
Figure Lengend Snippet: A Human neurons (1 month old) before and after acute treatment with norepinephrine stained for presynaptic markers Syph, synapsin (‘Pan-Syn’) and MAP2.
Article Snippet:
Techniques: Staining
Journal: Cell
Article Title: Neuromodulator Signaling Bidirectionally Controls Vesicle Numbers in Human Synapses
doi: 10.1016/j.cell.2019.09.011
Figure Lengend Snippet: A, B and C Puncta densities of acutely forskolin treated (10 µM, 30 mins) and control and Syn1-deficient human neurons stained for pan-Synapsin (A), Syt1 (A), Syph (B), Homer (C) and MAP2. Puncta areas are depicted in Figure S4.
Article Snippet:
Techniques: Control, Staining
Journal: Cell
Article Title: Neuromodulator Signaling Bidirectionally Controls Vesicle Numbers in Human Synapses
doi: 10.1016/j.cell.2019.09.011
Figure Lengend Snippet: Highlights:
Article Snippet:
Techniques: Transduction, Recombinant, Suspension, Plasmid Preparation, Expressing, Software