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anti-nestin/radial glial marker  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank anti-nestin/radial glial marker
    Anti Nestin/Radial Glial Marker, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 94/100, based on 15 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/nestin/anti-Nestin%2Fradial+glial+marker/custom%40rc2%4042480735
    Average 94 stars, based on 15 article reviews
    anti-nestin/radial glial marker - by Bioz Stars, 2026-09
    94/100 stars

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    Related Articles

    Incubation:

    Article Title: RNA-binding proteins mediate the maturation of chromatin topology during differentiation.
    Article Snippet: The coverslips were washed three times with DPBS (Gibco, 21600-069) for 5 min and permeabilized with 0.5% Triton X-100 (Bio-Rad, 1610407) for 15 min at RT. .. Samples were then incubated in blocking solution (0.5% BSA (BioShop, ALB001) in DPBS) for 1 h. Coverslips were incubated with primary antibodies Oct4 Nature Cell Biology Article https://doi.org/10.1038/s41556-025-01735-5 (1:400, Santa Cruz, sc-5279), Nestin (1:100, Developmental Studies Hybridoma Bank, rat-401), GFAP (1:200, Proteintech, 16825-1-AP) and Tubb3 (1:300, Proteintech, 66375-1-Ig) in blocking solution for 1 h at RT. ..

    Article Title: RNA-binding proteins mediate the maturation of chromatin topology during differentiation
    Article Snippet: The coverslips were washed three times with DPBS (Gibco, 21600-069) for 5 min and permeabilized with 0.5% Triton X-100 (Bio-Rad, 1610407) for 15 min at RT. .. Samples were then incubated in blocking solution (0.5% BSA (BioShop, ALB001) in DPBS) for 1 h. Coverslips were incubated with primary antibodies Oct4 (1:400, Santa Cruz, sc-5279), Nestin (1:100, Developmental Studies Hybridoma Bank, rat-401), GFAP (1:200, Proteintech, 16825-1-AP) and Tubb3 (1:300, Proteintech, 66375-1-Ig) in blocking solution for 1 h at RT. ..

    Blocking Assay:

    Article Title: RNA-binding proteins mediate the maturation of chromatin topology during differentiation.
    Article Snippet: The coverslips were washed three times with DPBS (Gibco, 21600-069) for 5 min and permeabilized with 0.5% Triton X-100 (Bio-Rad, 1610407) for 15 min at RT. .. Samples were then incubated in blocking solution (0.5% BSA (BioShop, ALB001) in DPBS) for 1 h. Coverslips were incubated with primary antibodies Oct4 Nature Cell Biology Article https://doi.org/10.1038/s41556-025-01735-5 (1:400, Santa Cruz, sc-5279), Nestin (1:100, Developmental Studies Hybridoma Bank, rat-401), GFAP (1:200, Proteintech, 16825-1-AP) and Tubb3 (1:300, Proteintech, 66375-1-Ig) in blocking solution for 1 h at RT. ..

    Article Title: RNA-binding proteins mediate the maturation of chromatin topology during differentiation
    Article Snippet: The coverslips were washed three times with DPBS (Gibco, 21600-069) for 5 min and permeabilized with 0.5% Triton X-100 (Bio-Rad, 1610407) for 15 min at RT. .. Samples were then incubated in blocking solution (0.5% BSA (BioShop, ALB001) in DPBS) for 1 h. Coverslips were incubated with primary antibodies Oct4 (1:400, Santa Cruz, sc-5279), Nestin (1:100, Developmental Studies Hybridoma Bank, rat-401), GFAP (1:200, Proteintech, 16825-1-AP) and Tubb3 (1:300, Proteintech, 66375-1-Ig) in blocking solution for 1 h at RT. ..

    Microscopy:

    Article Title: Methods for neural conversion of human embryonic stem cells
    Article Snippet: .. Primary antibodies used for microscopy included PAX6 (Covance), Oct4 (Biovision), AP2 (Novus Biologicals), GBX2 (Sigma), HNK1 (Sigma), HOXB4 (Developmental Studies Hybridoma Bank (DSHB)), Nestin (R&D), NKX6.1 (DSHB), OTX2 (gift), p75 (Advanced Target Systems.), PAX7 (DSHB), PLZF (Calbiochem), TUJI (Covance), ZO1 (Zymed), BF1 (FOXG1, gift Esseng Lai), TH (Sigma), HB9 (DSHB), ISL1 (DSHB). .. CD105-PE (eBioscience) was used for excluding MS5 stromal cells for flow cytometery on a FACS can (BD).

    other:





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    Image Search Results


    McERV-PTLVs specifically transduce cells of brain tumors induced by GSCs injection, leaving normal brain tissues untouched (A) Mice with intracranial tumor induced by GSCs were transduced with concentrated McERV-PTLVs encoding marker EGFP. Seven days after transduction, the brain was isolated, and first cut in coronal section by the injection holes was performed. (B) Fluorescence microscopy images representing the area of the first cut demonstrate the distribution of transduced cells expressing marker EGFP. Magnified images with signed white scale bar provided. White doted lines represent the EGFP-positive area. The small image at the left upper corner of the first picture is the coronal slice stained immunohistochemically with anti-nestin antibodies representing the tumor engraftment. (C) Control group of mice was injected with 1×PBS instead of GSCs and then with McERV-PTLVs. The brain of control mice was analyzed as written above. (D) Fluorescence microscopy images of the area of the first cut represent the absence of EGFP-positive cells. The scheme of the coronal section of caudate-putamen area, where injection holes were performed (marked with red-dotted square). The small image left from the first picture is the coronal slice stained immunohistochemically with anti-nestin antibodies representing the absence of tumor. (E) Mice with intracranial tumor induced by GSCs were transduced with concentrated VSVG-PTLVs encoding marker EGFP. Black-dotted arrow below represents the timescale. (F) The fluorescence microscopy images represent the more disseminated areas of EGFP-positive cells provided on several magnifications (pointed by white arrows). The small image at the left bottom corner of the first picture is the coronal slice stained immunohistochemically, with anti-nestin antibodies representing the tumor engraftment. (G) Images of hematoxylin/eosin staining (right column) and immunohistochemical staining of slices with anti-(human) nestin antibody. Black dotted line represents the area of tumor growth. The upper row samples obtained from mice injected with GSCs and McERV-PTLVs; middle row:1×PBS and McERV-PTLVs; bottom row: GSCs and VSVG-PTLVs. Black scale bars, 100 μm. (H) Fluorescence microscopy images of IF-stained slices obtained from mice with GSC-induced tumor and injected with McERV-PTLVs. DAPI: nuclei staining (blue); anti-(human) nestin mAb stained with Alexa 555 (Red) fluor-conjugated secondary Ab, EGFP: marker fluorescent protein indicates the cells transduced with McERV-PTLVs (the merged image of EGFP [green] and anti-nestin [red] pictures are represented). The white dotted line represents the nestin-positive area of tumor growth. (I) Fluorescence microscopy images of IF-stained slices obtained from mice of control group injected with 1×PBS and McERV PTLVs, representing the absence of nestin and EGFP-positive cells. (J) Fluorescence microscopy images of IF-stained slices obtained from mice with GSC-induced tumor and injected with VSVG-PTLVs. White scale bars on H, I, and J: 100 μm.

    Journal: Molecular Therapy Oncology

    Article Title: Targeted attack: Harnessing myelin-specific plasmolipin for suppression of neuroblastoma and glioblastoma

    doi: 10.1016/j.omton.2026.201154

    Figure Lengend Snippet: McERV-PTLVs specifically transduce cells of brain tumors induced by GSCs injection, leaving normal brain tissues untouched (A) Mice with intracranial tumor induced by GSCs were transduced with concentrated McERV-PTLVs encoding marker EGFP. Seven days after transduction, the brain was isolated, and first cut in coronal section by the injection holes was performed. (B) Fluorescence microscopy images representing the area of the first cut demonstrate the distribution of transduced cells expressing marker EGFP. Magnified images with signed white scale bar provided. White doted lines represent the EGFP-positive area. The small image at the left upper corner of the first picture is the coronal slice stained immunohistochemically with anti-nestin antibodies representing the tumor engraftment. (C) Control group of mice was injected with 1×PBS instead of GSCs and then with McERV-PTLVs. The brain of control mice was analyzed as written above. (D) Fluorescence microscopy images of the area of the first cut represent the absence of EGFP-positive cells. The scheme of the coronal section of caudate-putamen area, where injection holes were performed (marked with red-dotted square). The small image left from the first picture is the coronal slice stained immunohistochemically with anti-nestin antibodies representing the absence of tumor. (E) Mice with intracranial tumor induced by GSCs were transduced with concentrated VSVG-PTLVs encoding marker EGFP. Black-dotted arrow below represents the timescale. (F) The fluorescence microscopy images represent the more disseminated areas of EGFP-positive cells provided on several magnifications (pointed by white arrows). The small image at the left bottom corner of the first picture is the coronal slice stained immunohistochemically, with anti-nestin antibodies representing the tumor engraftment. (G) Images of hematoxylin/eosin staining (right column) and immunohistochemical staining of slices with anti-(human) nestin antibody. Black dotted line represents the area of tumor growth. The upper row samples obtained from mice injected with GSCs and McERV-PTLVs; middle row:1×PBS and McERV-PTLVs; bottom row: GSCs and VSVG-PTLVs. Black scale bars, 100 μm. (H) Fluorescence microscopy images of IF-stained slices obtained from mice with GSC-induced tumor and injected with McERV-PTLVs. DAPI: nuclei staining (blue); anti-(human) nestin mAb stained with Alexa 555 (Red) fluor-conjugated secondary Ab, EGFP: marker fluorescent protein indicates the cells transduced with McERV-PTLVs (the merged image of EGFP [green] and anti-nestin [red] pictures are represented). The white dotted line represents the nestin-positive area of tumor growth. (I) Fluorescence microscopy images of IF-stained slices obtained from mice of control group injected with 1×PBS and McERV PTLVs, representing the absence of nestin and EGFP-positive cells. (J) Fluorescence microscopy images of IF-stained slices obtained from mice with GSC-induced tumor and injected with VSVG-PTLVs. White scale bars on H, I, and J: 100 μm.

    Article Snippet: For immunohistochemical assessments, an antibody specific to human nestin (R&D Systems GmbH, Wiesbaden-Nordenstadt, Germany) was used.

    Techniques: Injection, Transduction, Marker, Isolation, Fluorescence, Microscopy, Expressing, Staining, Control, Immunohistochemical staining