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mouse anti n cadherin  (Developmental Studies Hybridoma Bank)


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    Developmental Studies Hybridoma Bank mouse anti n cadherin
    Mouse Anti N Cadherin, supplied by Developmental Studies Hybridoma Bank, used in various techniques. Bioz Stars score: 91/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mouse+anti+n+cadherin/anti-fibronectin/bio_rxiv__64898__2026__04__21__718480-249-34-36
    Average 91 stars, based on 1 article reviews
    mouse anti n cadherin - by Bioz Stars, 2026-09
    91/100 stars

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    Related Articles

    other:

    Article Title: MMP14 is required for delamination of chick neural crest cells independently of its catalytic activity
    Article Snippet: Antibodies used were custom-made polyclonal mouse anti-chick MMP14 (1/500), mouse anti-N-cadherin (DSHB, 6B3, 1/250), mouse anti-E-cadherin (BD Transduction Laboratories, 61081, 1/250), rabbit anti-snail2 (Cell Signaling, C19G7, 1/250), rabbit anti-Sox9 (Millipore, AB5535, 1/100), rabbit anti-sox10 (GeneTex GTX128374, 1/200), mouse anti-TFAP2α (DSHB, 3B5, 1/400), rabbit anti-PCM1 ( Dammermann and Merdes, 2002 ; 1/400), mouse anti-phospho-histone 3 (Ser10) (Cell Signaling, MA312B, 1/1000), mouse anti-laminin (DSHB, 3H11, 1/100), mouse anti-HNK1 (DSHB, 1C10, 1/50), mouse anti-aPKC (Santa Cruz, sc17781, 1/100), mouse anti-ZO1 (ThermoFisher, 33-9100, 1/200) and mouse anti-β-catenin (Sigma, C2206, 1/200).

    Article Title: Bone morphogenetic proteins regulate hinge point formation during neural tube closure by dynamic modulation of apicobasal polarity
    Article Snippet: The following primary antibodies were used for analyses: rabbit anti-pHH3 (Upstate; 1:500), rabbit anti-PAR3 (Upstate; 1:500), rabbit anti-phosphorylated (p)-SMAD 1,5,8 (Cell signaling; 1:1000), mouse anti-N-Cadherin (DSHB; 1:500), mouse anti-ZO-1 (BD biosciences; 1:1000); mouse anti-GFP (Molecular Probes; 1:500), Laminin (DSHB; 1:1000) and activated Caspase 3 (Cell Signaling; 1:200).

    Article Title: Basolateral localization of MMP14 drives apicobasal polarity change during EMT independently of its catalytic activity
    Article Snippet: Antibodies used: custom-made polyclonal mouse anti-chick MMP14, mouse anti-AP2 (DSHB, 3B5), mouse anti-Snail2 (Cell Signaling, C19B7), rabbit anti-Sox10 (GeneTex, GTX128374), rabbit anti-PCM1 , mouse anti-N-Cadherin (DSHB, 6B3), mouse anti-E-cadherin (BD Transduction Laboratories, 610181), mouse anti-phospho-histone 3 (Cell Signaling, MA312B), mouse anti-laminin (DSHB, 3H11).

    Article Title: Modelling variability and heterogeneity of EMT scenarios highlights nuclear positioning and protrusions as main drivers of extrusion
    Article Snippet: The following antibodies, mouse anti-N-cadherin (DSHB, 6B3), mouse anti-Sox9 (DSHB, DA1D1), mouse anti-Fibronectin (DSHB, B3/D6), mouse anti-TFAP2α (DSHB, 3B5), mouse anti-laminin (DSHB, 3H11), were obtained from the Developmental Studies Hybridoma Bank, created by the NICHD of the NIH and maintained at The University of Iowa, Department of Biology, Iowa City, IA 52242.

    Article Title: Modelling variability and heterogeneity of EMT scenarios highlights nuclear positioning and protrusions as main drivers of extrusion
    Article Snippet: The following antibodies, mouse anti-N-cadherin (DSHB, 6B3), mouse anti-Sox9 (DSHB, DA1D1), mouse anti-Fibronectin (DSHB, B3/D6), mouse anti-TFAP211(DSHB, 3B5), mouse anti-laminin (DSHB, 3H11), were obtained from the Developmental Studies Hybridoma Bank, created by the NICHD of the NIH and maintained at The University of Iowa, Department of Biology, Iowa City, IA 52242.

    Incubation:

    Article Title: TAR syndrome causal gene RBM8A is critical for embryonic bone development and proper Hedgehog signaling
    Article Snippet: .. Subsequently, they were incubated in 5% normal serum for 1 hour at room temperature, then incubated overnight at 4 °C in rabbit anti-RBM8A (GeneTex, catalog #: GTX131387), mouse anti-Fibronectin (DSHB Hybridoma, catalog #: P1H11), mouse anti-N-Cadherin (DSHB Hybridoma, catalog #: MNCD2-s), rabbit anti-Ki67 (Invitrogen, catalog #: 701198), or goat anti-SOX9 (R&D Systems, catalog #: AF3075). .. After staining, coverslips were mounted onto microscope slides using ProLong Diamond Antifade Mountant with DAPI (Invitrogen, catalog #: P36971).



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    RL-RF10 promotes p-EMT through integrins αv and β3. (A) Western blot analysis of p-EMT marker proteins in HOKs treated with RL-RF10. (B) Quantitative analysis of protein expression. (C) Immunofluorescence staining for vimentin and <t>N-cadherin</t> proteins, with fluorescence intensity represented in 3D surface plots. Scale bar = 20 μm. (D) Western blot analysis of integrins αv and β3. (E) Quantitative analysis of protein expression. (F) Immunofluorescence staining for integrins αv and β3, with 3D surface plots showing fluorescence intensity. Scale bar = 20 μm. Data are presented as mean ± SEM ( n = 3, * P < .05, ** P < .01).
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    Image Search Results


    RL-RF10 promotes p-EMT through integrins αv and β3. (A) Western blot analysis of p-EMT marker proteins in HOKs treated with RL-RF10. (B) Quantitative analysis of protein expression. (C) Immunofluorescence staining for vimentin and N-cadherin proteins, with fluorescence intensity represented in 3D surface plots. Scale bar = 20 μm. (D) Western blot analysis of integrins αv and β3. (E) Quantitative analysis of protein expression. (F) Immunofluorescence staining for integrins αv and β3, with 3D surface plots showing fluorescence intensity. Scale bar = 20 μm. Data are presented as mean ± SEM ( n = 3, * P < .05, ** P < .01).

    Journal: International Dental Journal

    Article Title: Frog-Derived Peptide RL-RF10 Facilitates Gingival Repair and Regeneration Through the Integrin αvβ3/p38/Snail1 Axis

    doi: 10.1016/j.identj.2025.109337

    Figure Lengend Snippet: RL-RF10 promotes p-EMT through integrins αv and β3. (A) Western blot analysis of p-EMT marker proteins in HOKs treated with RL-RF10. (B) Quantitative analysis of protein expression. (C) Immunofluorescence staining for vimentin and N-cadherin proteins, with fluorescence intensity represented in 3D surface plots. Scale bar = 20 μm. (D) Western blot analysis of integrins αv and β3. (E) Quantitative analysis of protein expression. (F) Immunofluorescence staining for integrins αv and β3, with 3D surface plots showing fluorescence intensity. Scale bar = 20 μm. Data are presented as mean ± SEM ( n = 3, * P < .05, ** P < .01).

    Article Snippet: The sliced tissues were incubated with the anti-N-cadherin mouse antibody (Servicebio).

    Techniques: Western Blot, Marker, Expressing, Immunofluorescence, Staining, Fluorescence

    RL-RF10 enhances gingival soft tissue regeneration in vivo. (A) Establishment of a New Zealand White Rabbit model with gingival tissue defects (created using BioRender). (B) Wound healing rates of gingival defects treated with RL-RF10. (C) H&E staining of tissue sections at different healing stages. Overview images (scale bar = 500 μm) with corresponding magnified views (scale bar = 200 μm) aligned in a right-hand column, linked by dashed lines. (D) Masson’s trichrome staining showing collagen fiber deposition during wound healing. For each group, the upper row displays overview images at sequential time points (scale bar = 500 μm), and the lower row directly beneath shows higher-magnification views of the corresponding boxed regions above, connected by dashed lines (scale bar = 200 μm). (E) Immunohistochemistry (IHC) analysis of N-cadherin expression in tissue sections. n = 3, * P < .05, ** P < .01.

    Journal: International Dental Journal

    Article Title: Frog-Derived Peptide RL-RF10 Facilitates Gingival Repair and Regeneration Through the Integrin αvβ3/p38/Snail1 Axis

    doi: 10.1016/j.identj.2025.109337

    Figure Lengend Snippet: RL-RF10 enhances gingival soft tissue regeneration in vivo. (A) Establishment of a New Zealand White Rabbit model with gingival tissue defects (created using BioRender). (B) Wound healing rates of gingival defects treated with RL-RF10. (C) H&E staining of tissue sections at different healing stages. Overview images (scale bar = 500 μm) with corresponding magnified views (scale bar = 200 μm) aligned in a right-hand column, linked by dashed lines. (D) Masson’s trichrome staining showing collagen fiber deposition during wound healing. For each group, the upper row displays overview images at sequential time points (scale bar = 500 μm), and the lower row directly beneath shows higher-magnification views of the corresponding boxed regions above, connected by dashed lines (scale bar = 200 μm). (E) Immunohistochemistry (IHC) analysis of N-cadherin expression in tissue sections. n = 3, * P < .05, ** P < .01.

    Article Snippet: The sliced tissues were incubated with the anti-N-cadherin mouse antibody (Servicebio).

    Techniques: In Vivo, Staining, Immunohistochemistry, Expressing