mouse smp14 mdm2 Search Results


mouse anti-mdm2  (Medaysis)
90
Medaysis mouse anti-mdm2
Strong and diffuse immunoreactivity of neoplastic cells to <t>MDM2</t> (immunohistochemical staining, bar = 100 μm).
Mouse Anti Mdm2, supplied by Medaysis, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Average 90 stars, based on 1 article reviews
mouse anti-mdm2 - by Bioz Stars, 2026-03
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Strong and diffuse immunoreactivity of neoplastic cells to MDM2 (immunohistochemical staining, bar = 100 μm).

Journal: Veterinary Research Forum

Article Title: Canine myxoid liposarcoma in Iran: a clinical report

doi: 10.30466/vrf.2022.558032.3561

Figure Lengend Snippet: Strong and diffuse immunoreactivity of neoplastic cells to MDM2 (immunohistochemical staining, bar = 100 μm).

Article Snippet: Then, 750 watt oven heat was used for two 5 min cycles for MDM2 marker (Mouse Anti-MDM2; Medaysis, Livermore, USA) and finally, for cooling, the sections were placed at room temperature for about 20 min. For confirmation, it was necessary to observe at least one positive nucleus in the power field of optical light microscope (400×).

Techniques: Immunohistochemical staining, Staining

Nuclear expression of MDM2 in neoplastic cells in myxoid liposarcoma. Nuclear expression of MDM2 was present in both spindle cells and lipocytic areas. Positive and negative cells were inter-mixed (immunohistochemical staining, bar = 50.00 μm).

Journal: Veterinary Research Forum

Article Title: Canine myxoid liposarcoma in Iran: a clinical report

doi: 10.30466/vrf.2022.558032.3561

Figure Lengend Snippet: Nuclear expression of MDM2 in neoplastic cells in myxoid liposarcoma. Nuclear expression of MDM2 was present in both spindle cells and lipocytic areas. Positive and negative cells were inter-mixed (immunohistochemical staining, bar = 50.00 μm).

Article Snippet: Then, 750 watt oven heat was used for two 5 min cycles for MDM2 marker (Mouse Anti-MDM2; Medaysis, Livermore, USA) and finally, for cooling, the sections were placed at room temperature for about 20 min. For confirmation, it was necessary to observe at least one positive nucleus in the power field of optical light microscope (400×).

Techniques: Expressing, Immunohistochemical staining, Staining