Review




Structured Review

Shanghai Model Organisms Center ngfr e
Ngfr E, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/e+ngfr/pmc12987631-158-9-16
Average 86 stars, based on 1 article reviews
ngfr e - by Bioz Stars, 2026-10
86/100 stars

Images

Related Articles

other:

Article Title: BM-derived mesenchymal stem cell microvesicles protect enteric neural precursor cells and alleviate diabetes-associated enteric neuropathy
Article Snippet: Nestin-creER T2 mice were bred with R26-e (CAG-RSR-LSL-DTRGFP-WPRE-pA) and Ngfr-e (2A-DreER T2 ) mice (purchased from Shanghai Model Organisms Center) to create Nestin-creER T2 × Ngfr-DreER T2 :DTRGFP mice.



Similar Products

86
Shanghai Model Organisms Center ngfr e
Ngfr E, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/e+ngfr/pmc12987631-158-9-16
Average 86 stars, based on 1 article reviews
ngfr e - by Bioz Stars, 2026-10
86/100 stars
  Buy from Supplier

86
Shanghai Model Organisms Center ngfr e 2a dreert2 mice
Ngfr E 2a Dreert2 Mice, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 86/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/2a+dreert2+ly6g+mice/10__1172_slash_jci192437-208-8-13
Average 86 stars, based on 1 article reviews
ngfr e 2a dreert2 mice - by Bioz Stars, 2026-10
86/100 stars
  Buy from Supplier

90
Shanghai Model Organisms Center ngfr-e (2 a-dreert2) mice
Ngfr E (2 A Dreert2) Mice, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/r26+e+cag+rsr+lsl+dtrgfp+wpre+pa/pm39468593-55-10-16
Average 90 stars, based on 1 article reviews
ngfr-e (2 a-dreert2) mice - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

90
Shanghai Model Organisms Center ngfr-e (2 a-dreer t2
Ngfr E (2 A Dreer T2, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/ngfr+e++2+a+dreer+t2/pmc11520590-44-11-19
Average 90 stars, based on 1 article reviews
ngfr-e (2 a-dreer t2 - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

90
Shanghai Model Organisms Center ngfr-e(2 a-dreert2) mice
Ngfr E(2 A Dreert2) Mice, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/r26+e+cag+rsr+lsl+dtrgfp+wpre+pa/pm37798789-48-7-12
Average 90 stars, based on 1 article reviews
ngfr-e(2 a-dreert2) mice - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

90
Shanghai Model Organisms Center ngfr-e(2 a-dreer t2 ) mice
L-Fucose improved the proliferation and differentiation abilities of injured ENPCs in vitro. A Cell morphology of primary ENPCs at days 2, 4, and 7. B Immunofluorescence staining showed cells within neurospheres co-expressed <t>Ngfr</t> (green) and Nestin (red), but immuno-negative for glial cell marker GFAP (green) or neuronal marker PGP9.5 (red). By inducing differentiation, neurons (PGP9.5, red), glial cells (GFAP, green), and smooth muscle cells (α-SMA, gray) were derived from neurospheres; the nuclei (blue). C Cell viability of ENPCs treated with different concentrations of L-Fucose for 72 h was determined by CCK8 assay. D Ki67 staining of ENPCs in each group. E The positive rate of Ki67 was analyzed in the statistical chart. F Representative immunofluorescence images of ENPCs-derived neurons (HuC/D, green) or glial cells (GFAP, green) in each group; the nuclei (blue). G The positive rate of HuC/D and GFAP were analyzed in the statistical chart. H Western blot analysis of HuC/D and GFAP proteins in each group. I Densitometric analysis of HuC/D and GFAP proteins in each group. Con: Primary ENPCs cultures; Glu: ENPCs treated with 30 mM glucose; Fuc: ENPCs treated with 30 mM glucose and 30 mg/ml L-Fucose. ENPCs, enteric neural precursor cells. Results were expressed as mean ± standard deviation. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001
Ngfr E(2 A Dreer T2 ) Mice, supplied by Shanghai Model Organisms Center, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/ngfr+e/ngfr+e+2+a+dreer+t2+++mice/pmc10552466-38-8-15
Average 90 stars, based on 1 article reviews
ngfr-e(2 a-dreer t2 ) mice - by Bioz Stars, 2026-10
90/100 stars
  Buy from Supplier

Image Search Results


L-Fucose improved the proliferation and differentiation abilities of injured ENPCs in vitro. A Cell morphology of primary ENPCs at days 2, 4, and 7. B Immunofluorescence staining showed cells within neurospheres co-expressed Ngfr (green) and Nestin (red), but immuno-negative for glial cell marker GFAP (green) or neuronal marker PGP9.5 (red). By inducing differentiation, neurons (PGP9.5, red), glial cells (GFAP, green), and smooth muscle cells (α-SMA, gray) were derived from neurospheres; the nuclei (blue). C Cell viability of ENPCs treated with different concentrations of L-Fucose for 72 h was determined by CCK8 assay. D Ki67 staining of ENPCs in each group. E The positive rate of Ki67 was analyzed in the statistical chart. F Representative immunofluorescence images of ENPCs-derived neurons (HuC/D, green) or glial cells (GFAP, green) in each group; the nuclei (blue). G The positive rate of HuC/D and GFAP were analyzed in the statistical chart. H Western blot analysis of HuC/D and GFAP proteins in each group. I Densitometric analysis of HuC/D and GFAP proteins in each group. Con: Primary ENPCs cultures; Glu: ENPCs treated with 30 mM glucose; Fuc: ENPCs treated with 30 mM glucose and 30 mg/ml L-Fucose. ENPCs, enteric neural precursor cells. Results were expressed as mean ± standard deviation. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001

Journal: Cell Communication and Signaling : CCS

Article Title: L-Fucose promotes enteric nervous system regeneration in type 1 diabetic mice by inhibiting SMAD2 signaling pathway in enteric neural precursor cells

doi: 10.1186/s12964-023-01311-0

Figure Lengend Snippet: L-Fucose improved the proliferation and differentiation abilities of injured ENPCs in vitro. A Cell morphology of primary ENPCs at days 2, 4, and 7. B Immunofluorescence staining showed cells within neurospheres co-expressed Ngfr (green) and Nestin (red), but immuno-negative for glial cell marker GFAP (green) or neuronal marker PGP9.5 (red). By inducing differentiation, neurons (PGP9.5, red), glial cells (GFAP, green), and smooth muscle cells (α-SMA, gray) were derived from neurospheres; the nuclei (blue). C Cell viability of ENPCs treated with different concentrations of L-Fucose for 72 h was determined by CCK8 assay. D Ki67 staining of ENPCs in each group. E The positive rate of Ki67 was analyzed in the statistical chart. F Representative immunofluorescence images of ENPCs-derived neurons (HuC/D, green) or glial cells (GFAP, green) in each group; the nuclei (blue). G The positive rate of HuC/D and GFAP were analyzed in the statistical chart. H Western blot analysis of HuC/D and GFAP proteins in each group. I Densitometric analysis of HuC/D and GFAP proteins in each group. Con: Primary ENPCs cultures; Glu: ENPCs treated with 30 mM glucose; Fuc: ENPCs treated with 30 mM glucose and 30 mg/ml L-Fucose. ENPCs, enteric neural precursor cells. Results were expressed as mean ± standard deviation. * p < 0.05, ** p < 0.01, *** p < 0.001, **** p < 0.0001

Article Snippet: Nestin-creER T2 mice were crossed with R26-e(CAG-RSR-LSL-DTRGFP-WPRE-pA) and Ngfr-e(2 A-DreER T2 ) mice (purchased from Shanghai Model Organisms Center, Inc) to generate Nestin-creER T2 × Ngfr-DreER T2 : DTRGFP triple transgenic mice, which specially labeled newborn Nestin + /Ngfr + cells with green fluorescent protein (GFP) after tamoxifen (TAM) induction (Additional file : Fig. S1A).

Techniques: In Vitro, Immunofluorescence, Staining, Marker, Derivative Assay, CCK-8 Assay, Western Blot, Standard Deviation