mouse anti-te7 Search Results


te7 monoclonal mouse anti-human antibody ab cbl271  (Merck KGaA)
90
Merck KGaA te7 monoclonal mouse anti-human antibody ab cbl271
Te7 Monoclonal Mouse Anti Human Antibody Ab Cbl271, supplied by Merck KGaA, 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/mouse+anti-te7/te+7+antibody/pm26506852-75-15-25
Average 90 stars, based on 1 article reviews
te7 monoclonal mouse anti-human antibody ab cbl271 - by Bioz Stars, 2026-09
90/100 stars
  Buy from Supplier
mouse anti te7 fibroblast antibody  (Novus Biologicals)
94
Novus Biologicals mouse anti te7 fibroblast antibody
Mouse Anti Te7 Fibroblast Antibody, supplied by Novus Biologicals, used in various techniques. Bioz Stars score: 94/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti-te7/Fibroblasts+Antibody+(TE-7)/pm37345150-49-53-56
Average 94 stars, based on 1 article reviews
mouse anti te7 fibroblast antibody - by Bioz Stars, 2026-09
94/100 stars
  Buy from Supplier
anti human thymic fibroblasts te7  (Santa Cruz Biotechnology)
93
Santa Cruz Biotechnology anti human thymic fibroblasts te7
Summarized characterization results for the pCL and cGCL grouped according to GFAP expression
Anti Human Thymic Fibroblasts Te7, supplied by Santa Cruz Biotechnology, used in various techniques. Bioz Stars score: 93/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/mouse+anti-te7/Human+Thymic+Fibroblasts+Antibody/pmc08451382-113-87-91
Average 93 stars, based on 1 article reviews
anti human thymic fibroblasts te7 - by Bioz Stars, 2026-09
93/100 stars
  Buy from Supplier

Image Search Results


Summarized characterization results for the pCL and cGCL grouped according to GFAP expression

Journal: Cancer Reports

Article Title: Characterization of adherent primary cell lines from fresh human glioblastoma tissue, defining glial fibrillary acidic protein as a reliable marker in establishment of glioblastoma cell culture

doi: 10.1002/cnr2.1324

Figure Lengend Snippet: Summarized characterization results for the pCL and cGCL grouped according to GFAP expression

Article Snippet: To visualize expression and cellular distribution of different marker proteins, the following primary and secondary antibodies were used: mouse monoclonal anti‐GFAP (Merck Millipore, Burlington, Massachusetts; 1:250), mouse monoclonal anti‐S100 (ß‐subunit) (Sigma‐Aldrich, St. Louis, Missouri; 1:200), rabbit polyclonal anti‐beta III Tubulin (TUBB3, abcam, Cambridge, UK; 1:1000), mouse monoclonal anti‐Vimentin (clone Vim 3B4, DakoCytomation, Glostrup, Denmark; 1:100), rabbit polyclonal anti‐Ki‐67 (H‐300) (MKI67, Santa Cruz Biotechnology, Dallas, Texas; 1:250), mouse monoclonal anti‐Nestin (10C2) (NES, abcam, Cambridge, UK; 1:100), mouse monoclonal anti‐Sox2 (L1D6A2) (Cell Signaling Technology, Danvers, Massachusetts; 1:400), mouse monoclonal anti‐Human Thymic Fibroblasts (TE7) (Santa Cruz Biotechnology, Dallas, Texas; 1:500), goat anti‐Mouse IgG‐FITC, and goat anti‐Rabbit IgG‐FITC (both Sigma‐Aldrich, St. Louis, Missouri; 1:200).

Techniques: Expressing, Migration

Immunocytochemical staining of pGCL. Examples for specific staining of GFAP, S100B, NES, and TE7 (green, FITC) in each GFAP expression group are given. Cell nuclei were counterstained with H33258 (blue). Magnification ×200. A, High GFAP expression group, B, medium GFAP expression group, and C, low GFAP expression group

Journal: Cancer Reports

Article Title: Characterization of adherent primary cell lines from fresh human glioblastoma tissue, defining glial fibrillary acidic protein as a reliable marker in establishment of glioblastoma cell culture

doi: 10.1002/cnr2.1324

Figure Lengend Snippet: Immunocytochemical staining of pGCL. Examples for specific staining of GFAP, S100B, NES, and TE7 (green, FITC) in each GFAP expression group are given. Cell nuclei were counterstained with H33258 (blue). Magnification ×200. A, High GFAP expression group, B, medium GFAP expression group, and C, low GFAP expression group

Article Snippet: To visualize expression and cellular distribution of different marker proteins, the following primary and secondary antibodies were used: mouse monoclonal anti‐GFAP (Merck Millipore, Burlington, Massachusetts; 1:250), mouse monoclonal anti‐S100 (ß‐subunit) (Sigma‐Aldrich, St. Louis, Missouri; 1:200), rabbit polyclonal anti‐beta III Tubulin (TUBB3, abcam, Cambridge, UK; 1:1000), mouse monoclonal anti‐Vimentin (clone Vim 3B4, DakoCytomation, Glostrup, Denmark; 1:100), rabbit polyclonal anti‐Ki‐67 (H‐300) (MKI67, Santa Cruz Biotechnology, Dallas, Texas; 1:250), mouse monoclonal anti‐Nestin (10C2) (NES, abcam, Cambridge, UK; 1:100), mouse monoclonal anti‐Sox2 (L1D6A2) (Cell Signaling Technology, Danvers, Massachusetts; 1:400), mouse monoclonal anti‐Human Thymic Fibroblasts (TE7) (Santa Cruz Biotechnology, Dallas, Texas; 1:500), goat anti‐Mouse IgG‐FITC, and goat anti‐Rabbit IgG‐FITC (both Sigma‐Aldrich, St. Louis, Missouri; 1:200).

Techniques: Staining, Expressing

Immunocytochemical characterization of the primary glioblastoma cell lines (pGCL). A, GFAP expression in the cultivated primary glioblastoma cell lines. B‐F, Positive stained cells (mean percentage) in pGCL grouped by GFAP expression. B, S100B, C, NES, D, TE7, E, SOX2, F, MKI67. G, SOX2 positive stained cells (mean percentage) in pGCL grouped by Nestin expression. H, MKI67 positive stained cells (mean percentage) in pGCL grouped by doubling time

Journal: Cancer Reports

Article Title: Characterization of adherent primary cell lines from fresh human glioblastoma tissue, defining glial fibrillary acidic protein as a reliable marker in establishment of glioblastoma cell culture

doi: 10.1002/cnr2.1324

Figure Lengend Snippet: Immunocytochemical characterization of the primary glioblastoma cell lines (pGCL). A, GFAP expression in the cultivated primary glioblastoma cell lines. B‐F, Positive stained cells (mean percentage) in pGCL grouped by GFAP expression. B, S100B, C, NES, D, TE7, E, SOX2, F, MKI67. G, SOX2 positive stained cells (mean percentage) in pGCL grouped by Nestin expression. H, MKI67 positive stained cells (mean percentage) in pGCL grouped by doubling time

Article Snippet: To visualize expression and cellular distribution of different marker proteins, the following primary and secondary antibodies were used: mouse monoclonal anti‐GFAP (Merck Millipore, Burlington, Massachusetts; 1:250), mouse monoclonal anti‐S100 (ß‐subunit) (Sigma‐Aldrich, St. Louis, Missouri; 1:200), rabbit polyclonal anti‐beta III Tubulin (TUBB3, abcam, Cambridge, UK; 1:1000), mouse monoclonal anti‐Vimentin (clone Vim 3B4, DakoCytomation, Glostrup, Denmark; 1:100), rabbit polyclonal anti‐Ki‐67 (H‐300) (MKI67, Santa Cruz Biotechnology, Dallas, Texas; 1:250), mouse monoclonal anti‐Nestin (10C2) (NES, abcam, Cambridge, UK; 1:100), mouse monoclonal anti‐Sox2 (L1D6A2) (Cell Signaling Technology, Danvers, Massachusetts; 1:400), mouse monoclonal anti‐Human Thymic Fibroblasts (TE7) (Santa Cruz Biotechnology, Dallas, Texas; 1:500), goat anti‐Mouse IgG‐FITC, and goat anti‐Rabbit IgG‐FITC (both Sigma‐Aldrich, St. Louis, Missouri; 1:200).

Techniques: Expressing, Staining