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2de  (FUJIFILM VisualSonics Inc)

 
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    Structured Review

    FUJIFILM VisualSonics Inc 2de
    2de, supplied by FUJIFILM VisualSonics Inc, 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/2de/2de/pm20512997-53-1-15
    Average 90 stars, based on 1 article reviews
    2de - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Two-Dimensional Gel Electrophoresis:

    Article Title: Hypertrophic cardiomyopathy and dysregulation of cardiac energetics in a mouse model of biliary fibrosis.
    Article Snippet: Continuous electrocardiograms (EC Genie, Mouse Systems Inc., Quincy, MA) and tail-cuff blood pressures (six-channel NIBP system with BPMONWIN software [IITC Life Science Inc., Woodland Hills, CA]) were recorded noninvasively in unsedated mice. .. Two-dimensional echocardiography (2DE) was performed in the MPC on sedated mice (Vevo 770 Digital RF, VisualSonic Inc. Toronto, CN). .. Cardiac magnetic resonance imaging (Bruker Biospin, Billerica, MA) was performed in sedated mice and analyzed by a blinded investigator as described previously15 (See Supporting Information).



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    Fig. 2. Two-dimensional <t>(2DE)</t> separations and immunoblot analysis of Trimeresurus albolabris venom. 2DE gels stained with silver stain, spots were numbered, grouped and alphabetically listed from A–P (A). 2DE immunoblot of Trimeresurus albolabris proteins probed with hemato polyvalent antivenom (B). Identification and relative classification of immunoreactive proteins (C) and non-immunoreactive proteins (D) in Trimeresurus albolabris venom .
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    Fig. 2. Two-dimensional (2DE) separations and immunoblot analysis of Trimeresurus albolabris venom. 2DE gels stained with silver stain, spots were numbered, grouped and alphabetically listed from A–P (A). 2DE immunoblot of Trimeresurus albolabris proteins probed with hemato polyvalent antivenom (B). Identification and relative classification of immunoreactive proteins (C) and non-immunoreactive proteins (D) in Trimeresurus albolabris venom .

    Journal: Scientific reports

    Article Title: Comparative in vitro immunoreactivity and protein analysis of Trimeresurus albolabris and Tropidolaemus wagleri venoms.

    doi: 10.1038/s41598-025-97032-0

    Figure Lengend Snippet: Fig. 2. Two-dimensional (2DE) separations and immunoblot analysis of Trimeresurus albolabris venom. 2DE gels stained with silver stain, spots were numbered, grouped and alphabetically listed from A–P (A). 2DE immunoblot of Trimeresurus albolabris proteins probed with hemato polyvalent antivenom (B). Identification and relative classification of immunoreactive proteins (C) and non-immunoreactive proteins (D) in Trimeresurus albolabris venom .

    Article Snippet: The separated polypeptide spots from 2DE gels were transferred to nitrocellulose membrane for 90 min at 18 V on a Trans-blot semi-dry Transfer CellTM (Biorad) in semi-dry transfer buffer (48 mM Tris and 2.93 g glycine) pH 9.2 containing 20% methanol.

    Techniques: Western Blot, Staining, Silver Staining

    Fig. 3. 2DE separations and immunoblot analysis of Tropidolaemus wagleri venom. 2DE gels stained with silver stain, spots were numbered, grouped and alphabetically listed from A–K (A). 2DE immunoblot of Tropidolaemus wagleri probed with hemato polyvalent antivenom (B). Identification and relative classification of immunoreactive proteins (C) and non-immunoreactive proteins (D) in Tropidolaemus wagleri venom.

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    Article Title: Comparative in vitro immunoreactivity and protein analysis of Trimeresurus albolabris and Tropidolaemus wagleri venoms.

    doi: 10.1038/s41598-025-97032-0

    Figure Lengend Snippet: Fig. 3. 2DE separations and immunoblot analysis of Tropidolaemus wagleri venom. 2DE gels stained with silver stain, spots were numbered, grouped and alphabetically listed from A–K (A). 2DE immunoblot of Tropidolaemus wagleri probed with hemato polyvalent antivenom (B). Identification and relative classification of immunoreactive proteins (C) and non-immunoreactive proteins (D) in Tropidolaemus wagleri venom.

    Article Snippet: The separated polypeptide spots from 2DE gels were transferred to nitrocellulose membrane for 90 min at 18 V on a Trans-blot semi-dry Transfer CellTM (Biorad) in semi-dry transfer buffer (48 mM Tris and 2.93 g glycine) pH 9.2 containing 20% methanol.

    Techniques: Western Blot, Staining, Silver Staining