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mouse anti syn  (Boster Bio)


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    Structured Review

    Boster Bio mouse anti syn
    Mouse Anti Syn, supplied by Boster Bio, used in various techniques. Bioz Stars score: 91/100, based on 3 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/result/mouse anti syn/product/Boster Bio
    Average 91 stars, based on 3 article reviews
    mouse anti syn - by Bioz Stars, 2026-03
    91/100 stars

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    Photomicrographs showing immunohistochemistry for neuronal markers . (a) neuron-specific enolase (NSE), (b) microtubule-associated protein-2 (MAP-2), (c) <t>Synaptophysin,</t> (d) neuronal nuclear antigen (NeuN), (e) tubulin, βIII isoform (TuJ1). The markers in a-d were diffusely positive in the part of the tumor with neuronal differentiation. However, TuJ1 was only weakly positive there. Olig2-positive cells were also observed in the same area (f). The cells comprising the perivascular pseudorosette were strongly positive for NSE (g) and MAP-2 (h), a-f: ×100; g and h: ×200.
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    Photomicrographs showing immunohistochemistry for neuronal markers . (a) neuron-specific enolase (NSE), (b) microtubule-associated protein-2 (MAP-2), (c) <t>Synaptophysin,</t> (d) neuronal nuclear antigen (NeuN), (e) tubulin, βIII isoform (TuJ1). The markers in a-d were diffusely positive in the part of the tumor with neuronal differentiation. However, TuJ1 was only weakly positive there. Olig2-positive cells were also observed in the same area (f). The cells comprising the perivascular pseudorosette were strongly positive for NSE (g) and MAP-2 (h), a-f: ×100; g and h: ×200.
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    Image Search Results


    Photomicrographs showing immunohistochemistry for neuronal markers . (a) neuron-specific enolase (NSE), (b) microtubule-associated protein-2 (MAP-2), (c) Synaptophysin, (d) neuronal nuclear antigen (NeuN), (e) tubulin, βIII isoform (TuJ1). The markers in a-d were diffusely positive in the part of the tumor with neuronal differentiation. However, TuJ1 was only weakly positive there. Olig2-positive cells were also observed in the same area (f). The cells comprising the perivascular pseudorosette were strongly positive for NSE (g) and MAP-2 (h), a-f: ×100; g and h: ×200.

    Journal: Diagnostic Pathology

    Article Title: Intraventricular glioneuronal tumor with disseminated lesions at diagnosis - a case report -

    doi: 10.1186/1746-1596-6-119

    Figure Lengend Snippet: Photomicrographs showing immunohistochemistry for neuronal markers . (a) neuron-specific enolase (NSE), (b) microtubule-associated protein-2 (MAP-2), (c) Synaptophysin, (d) neuronal nuclear antigen (NeuN), (e) tubulin, βIII isoform (TuJ1). The markers in a-d were diffusely positive in the part of the tumor with neuronal differentiation. However, TuJ1 was only weakly positive there. Olig2-positive cells were also observed in the same area (f). The cells comprising the perivascular pseudorosette were strongly positive for NSE (g) and MAP-2 (h), a-f: ×100; g and h: ×200.

    Article Snippet: The primary antibodies and their dilution with buffer were as follows: rabbit polyclonal anti-olig2 antibody (1:200; Millipore, Temecula, CA), polyclonal anti-vimentin antibody (1:200; Dako, Glostrup, Denmark), mouse monoclonal anti-glial fibrillary acidic protein (GFAP) antibody (1:500; Dako), mouse monoclonal anti-synaptophysin (Syn) antibody (1:50; Millipore), mouse monoclonal anti-tubulin, βIII isoform (TuJ1) antibody (1:200; Millipore), monoclonal anti-neuronal nuclear antigen (Neu-N) antibody (1:100; Millipore), monoclonal anti-microtubule associated protein-2 (MAP-2) antibody (1:100; Millipore), monoclonal anti-neuron-specific enolase (NSE) and monoclonal anti-Ki-67/MIB-1 antibody (1:50; Dako).

    Techniques: Immunohistochemistry