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dapi  (Vector Laboratories)


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    Structured Review

    Vector Laboratories dapi
    Dapi, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 96/100, based on 3097 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/mounting+medium+containing+dapi/VECTASHIELD+Hardset+Antifade+Mounting+Medium+with+DAPI/pm42757461-74-5-9
    Average 96 stars, based on 3097 article reviews
    dapi - by Bioz Stars, 2026-10
    96/100 stars

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    Related Articles

    Staining:

    Article Title: The basic domain of Suv39h2 buffers mitoxantrone-induced heterochromatin destabilization
    Article Snippet: .. Subsequently, slides were stained with antibodies against NPM1 (ab10530, Abcam; 1:1000) and HP1α (ab109028, Abcam; 1:1000), then mounted with VECTASHIELD containing DAPI (Vector Laboratories, H-1200-10). .. Imaging was performed using a Zeiss LSM880 confocal microscope with a 63×objective.

    Article Title: Dual-function oral nanotherapeutic mitigates sepsis-like multi-organ failure by targeting inflammatory and fibrotic pathways
    Article Snippet: .. Thereafter, sections were stained with a recombinant rabbit monoclonal antibody against Nlrp3 (invitrogen, Cat#: MA5-32255, RRID: AB_2809541 ), Casp1 p20 (cleaved Asp296) polyclonal antibody (invitrogen, Cat#: PA5-99390, RRID: AB_2818323 ), and Nek7 polyclonal antibody (invitrogen, Cat#: PA5-101861, RRID: AB_2851293 ) at 1:100 dilution in 1.5% horse serum in PBS, while NF-κB p65 was incubated with mouse monoclonal antibody (SantaCruz, Cat#: A-12 sc: 514451, RRID: AB_2891257 ) at 1:25 dilution overnight at 4 °C followed by secondary antibody [goat anti-rabbit IgG Alexa Flour-488 (Nlrp3 and Nek7) and 594 (Casp1 and NF-κB p65)] at 1:1000 dilution in PBS for 2 h. Sections were then washed 3 times with PBS and counterstained with DAPI (1:1000 dilution) for 5 min and subsequently washed with PBS one time before sections were cover-slipped with mounting media containing DAPI (Vectorshield, H-1800, Vector laboratories). .. After staining, all slides were visualized/scanned under LSM-900 Zeiss/Axioscan 7 confocal microscope and images were processed with Zen blue 3.3 software and quantified with ImageJ software.

    Article Title: MMRi62 induces iron depletion–driven apoptosis through a ferritin-independent mechanism
    Article Snippet: Coverslips were subsequently washed three times with PBS and incubated with fluorescently labelled phalloidin (1:500; Cytoskeleton, PHDH1-A) for 1 h at room temperature to visualize the actin cytoskeleton. .. Following three additional washes with PBS, coverslips were mounted onto microscope slides using mounting medium containing DAPI (Vector Laboratories, Burlingame, CA, USA) for nuclear staining. .. Fluorescence images were acquired using a Zeiss fluorescence microscope (Carl Zeiss Microscopy GmbH, Jena, Germany) and processed using Zeiss imaging software (Carl Zeiss Microscopy GmbH, Jena, Germany).

    Article Title: Thermoreversible cell-derived extracellular matrix only hydrogel (CEOgel): Development, characterization, and applications
    Article Snippet: After quick freezing, the CEO gel was cryo-sectioned at a thickness of 8 μm using a freezing microtome (Epredia HM 525 NX Cryostat Package, Epredia, MI, USA) and stained with Brilliant Blue R Staining Solution (B6529, Sigma-Aldrich) for 10 min at RT to visualize total proteins. .. After several washes, the samples were incubated with secondary antibodies for 1 h at RT and then mounted with Vectashield® mounting medium containing 4, 6-diamidino-2-phenylindole (DAPI) (H1200; Vector Lab, Burlingame, CA, USA) for counter staining. .. The primary and secondary antibodies used were as follows: rabbit monoclonal anti-collagen type I (ab138492, Abcam, Cambridge, UK, 1:500), rabbit polyclonal anti-laminin (L9393, Sigma-Aldrich, 1:100), mouse monoclonal anti-fibronectin (SC-8422; Santa Cruz Biotechnology, 1:200), Alexa Fluor® 488-conjugated goat anti-rabbit IgG (A-11008; Invitrogen, Waltham, MA, USA), and Alexa Fluor® 594-conjugated goat anti-mouse IgG (A-11005; Invitrogen).

    Recombinant:

    Article Title: Dual-function oral nanotherapeutic mitigates sepsis-like multi-organ failure by targeting inflammatory and fibrotic pathways
    Article Snippet: .. Thereafter, sections were stained with a recombinant rabbit monoclonal antibody against Nlrp3 (invitrogen, Cat#: MA5-32255, RRID: AB_2809541 ), Casp1 p20 (cleaved Asp296) polyclonal antibody (invitrogen, Cat#: PA5-99390, RRID: AB_2818323 ), and Nek7 polyclonal antibody (invitrogen, Cat#: PA5-101861, RRID: AB_2851293 ) at 1:100 dilution in 1.5% horse serum in PBS, while NF-κB p65 was incubated with mouse monoclonal antibody (SantaCruz, Cat#: A-12 sc: 514451, RRID: AB_2891257 ) at 1:25 dilution overnight at 4 °C followed by secondary antibody [goat anti-rabbit IgG Alexa Flour-488 (Nlrp3 and Nek7) and 594 (Casp1 and NF-κB p65)] at 1:1000 dilution in PBS for 2 h. Sections were then washed 3 times with PBS and counterstained with DAPI (1:1000 dilution) for 5 min and subsequently washed with PBS one time before sections were cover-slipped with mounting media containing DAPI (Vectorshield, H-1800, Vector laboratories). .. After staining, all slides were visualized/scanned under LSM-900 Zeiss/Axioscan 7 confocal microscope and images were processed with Zen blue 3.3 software and quantified with ImageJ software.

    Incubation:

    Article Title: Dual-function oral nanotherapeutic mitigates sepsis-like multi-organ failure by targeting inflammatory and fibrotic pathways
    Article Snippet: .. Thereafter, sections were stained with a recombinant rabbit monoclonal antibody against Nlrp3 (invitrogen, Cat#: MA5-32255, RRID: AB_2809541 ), Casp1 p20 (cleaved Asp296) polyclonal antibody (invitrogen, Cat#: PA5-99390, RRID: AB_2818323 ), and Nek7 polyclonal antibody (invitrogen, Cat#: PA5-101861, RRID: AB_2851293 ) at 1:100 dilution in 1.5% horse serum in PBS, while NF-κB p65 was incubated with mouse monoclonal antibody (SantaCruz, Cat#: A-12 sc: 514451, RRID: AB_2891257 ) at 1:25 dilution overnight at 4 °C followed by secondary antibody [goat anti-rabbit IgG Alexa Flour-488 (Nlrp3 and Nek7) and 594 (Casp1 and NF-κB p65)] at 1:1000 dilution in PBS for 2 h. Sections were then washed 3 times with PBS and counterstained with DAPI (1:1000 dilution) for 5 min and subsequently washed with PBS one time before sections were cover-slipped with mounting media containing DAPI (Vectorshield, H-1800, Vector laboratories). .. After staining, all slides were visualized/scanned under LSM-900 Zeiss/Axioscan 7 confocal microscope and images were processed with Zen blue 3.3 software and quantified with ImageJ software.

    Article Title: Thermoreversible cell-derived extracellular matrix only hydrogel (CEOgel): Development, characterization, and applications
    Article Snippet: After quick freezing, the CEO gel was cryo-sectioned at a thickness of 8 μm using a freezing microtome (Epredia HM 525 NX Cryostat Package, Epredia, MI, USA) and stained with Brilliant Blue R Staining Solution (B6529, Sigma-Aldrich) for 10 min at RT to visualize total proteins. .. After several washes, the samples were incubated with secondary antibodies for 1 h at RT and then mounted with Vectashield® mounting medium containing 4, 6-diamidino-2-phenylindole (DAPI) (H1200; Vector Lab, Burlingame, CA, USA) for counter staining. .. The primary and secondary antibodies used were as follows: rabbit monoclonal anti-collagen type I (ab138492, Abcam, Cambridge, UK, 1:500), rabbit polyclonal anti-laminin (L9393, Sigma-Aldrich, 1:100), mouse monoclonal anti-fibronectin (SC-8422; Santa Cruz Biotechnology, 1:200), Alexa Fluor® 488-conjugated goat anti-rabbit IgG (A-11008; Invitrogen, Waltham, MA, USA), and Alexa Fluor® 594-conjugated goat anti-mouse IgG (A-11005; Invitrogen).

    Microscopy:

    Article Title: MMRi62 induces iron depletion–driven apoptosis through a ferritin-independent mechanism
    Article Snippet: Coverslips were subsequently washed three times with PBS and incubated with fluorescently labelled phalloidin (1:500; Cytoskeleton, PHDH1-A) for 1 h at room temperature to visualize the actin cytoskeleton. .. Following three additional washes with PBS, coverslips were mounted onto microscope slides using mounting medium containing DAPI (Vector Laboratories, Burlingame, CA, USA) for nuclear staining. .. Fluorescence images were acquired using a Zeiss fluorescence microscope (Carl Zeiss Microscopy GmbH, Jena, Germany) and processed using Zeiss imaging software (Carl Zeiss Microscopy GmbH, Jena, Germany).



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