s100b egfp 1wjt l Search Results


s100b egfp 1wjt l  (Jackson Laboratory)
86
Jackson Laboratory s100b egfp 1wjt l
S100b Egfp 1wjt L, supplied by Jackson Laboratory, 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/s100b+egfp+1wjt+l/1100mjb+6+c57bl+j+tcratcrb+tg/pm41950328-370-8-13
Average 86 stars, based on 1 article reviews
s100b egfp 1wjt l - by Bioz Stars, 2026-10
86/100 stars
  Buy from Supplier
transgenic mouse models  (Jackson Laboratory)
86
Jackson Laboratory transgenic mouse models
Immunofluorescence micrographs represent the linage tracing analysis of sciatic nerve tissue 7 days after crush injury followed by EFF or sham TNT, showing GFP linage tracer expression in <t>transgenic</t> mouse models to identify cells originating from ( A ) Schwann cells <t>(S100B)</t> or ( B ) fibroblasts (S100A4). ( C ) Histological analysis revealed increased CD31 expression in the EFF TNT-treated group compared to the sham group in the S100B-EGFP mouse model, demonstrating successful vasculogenic reprogramming. ( D ) However, there was little to no increase in coassociation of the lineage tracer for S100B (GFP, green) with the endothelial marker (CD31, red) and cell nuclei (DAPI, blue) compared to the sham group. ( E ) In contrast, the S100A4-EGFP mouse model showed significantly higher expression of CD31 in the EFF treatment compared to the sham group and ( F ) a significant increase in coassociation between GFP-labeled fibroblasts with CD31 and DAPI in response to EFF TNT, suggesting that fibroblasts are the predominant contributors to the newly formed vascular cell population induced by reprogramming. All error bars are shown as SEM; * denotes significant difference with respect to sham with a P value < 0.05, two-tailed t -test.
Transgenic Mouse Models, supplied by Jackson Laboratory, 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/s100b+egfp+1wjt+l/model+mouse/pmc13060591-325-4-10
Average 86 stars, based on 1 article reviews
transgenic mouse models - by Bioz Stars, 2026-10
86/100 stars
  Buy from Supplier

Image Search Results


Immunofluorescence micrographs represent the linage tracing analysis of sciatic nerve tissue 7 days after crush injury followed by EFF or sham TNT, showing GFP linage tracer expression in transgenic mouse models to identify cells originating from ( A ) Schwann cells (S100B) or ( B ) fibroblasts (S100A4). ( C ) Histological analysis revealed increased CD31 expression in the EFF TNT-treated group compared to the sham group in the S100B-EGFP mouse model, demonstrating successful vasculogenic reprogramming. ( D ) However, there was little to no increase in coassociation of the lineage tracer for S100B (GFP, green) with the endothelial marker (CD31, red) and cell nuclei (DAPI, blue) compared to the sham group. ( E ) In contrast, the S100A4-EGFP mouse model showed significantly higher expression of CD31 in the EFF treatment compared to the sham group and ( F ) a significant increase in coassociation between GFP-labeled fibroblasts with CD31 and DAPI in response to EFF TNT, suggesting that fibroblasts are the predominant contributors to the newly formed vascular cell population induced by reprogramming. All error bars are shown as SEM; * denotes significant difference with respect to sham with a P value < 0.05, two-tailed t -test.

Journal: Science Advances

Article Title: Vasculogenic tissue nanotransfection accelerates functional recovery after peripheral nerve injury

doi: 10.1126/sciadv.aeb7631

Figure Lengend Snippet: Immunofluorescence micrographs represent the linage tracing analysis of sciatic nerve tissue 7 days after crush injury followed by EFF or sham TNT, showing GFP linage tracer expression in transgenic mouse models to identify cells originating from ( A ) Schwann cells (S100B) or ( B ) fibroblasts (S100A4). ( C ) Histological analysis revealed increased CD31 expression in the EFF TNT-treated group compared to the sham group in the S100B-EGFP mouse model, demonstrating successful vasculogenic reprogramming. ( D ) However, there was little to no increase in coassociation of the lineage tracer for S100B (GFP, green) with the endothelial marker (CD31, red) and cell nuclei (DAPI, blue) compared to the sham group. ( E ) In contrast, the S100A4-EGFP mouse model showed significantly higher expression of CD31 in the EFF treatment compared to the sham group and ( F ) a significant increase in coassociation between GFP-labeled fibroblasts with CD31 and DAPI in response to EFF TNT, suggesting that fibroblasts are the predominant contributors to the newly formed vascular cell population induced by reprogramming. All error bars are shown as SEM; * denotes significant difference with respect to sham with a P value < 0.05, two-tailed t -test.

Article Snippet: For linage tracing experiments, transgenic mouse models B6;D2-Tg(S100B-EGFP)1Wjt/l and B6.Cg-Tg(S100a4-EGFP)M1Egn/YunkJ (the Jackson Laboratory) were used to trace different cell populations in the sciatic nerve, expressing GFP in Schwann cells and fibroblasts, respectively.

Techniques: Immunofluorescence, Expressing, Transgenic Assay, Marker, Labeling, Two Tailed Test