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microarray glass slide with dapi  (Thermo Fisher)


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    Thermo Fisher microarray glass slide with dapi
    Microarray Glass Slide With Dapi, supplied by Thermo Fisher, used in various techniques. Bioz Stars score: 99/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/tissue+microarray+analysis+tissue+microarray+slides/PBS/pmc05067491__ncomms13182___s1-39-13-18
    Average 99 stars, based on 1 article reviews
    microarray glass slide with dapi - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    other:

    Article Title: Derivatives of dolaproine-dolaisoleuine peptides
    Article Snippet: After 72 h of acclimatization, the mice are implanted with SW780 human bladder cancer cells (2×106 cells/mouse), suspended in 50% complete cultrex (Trevigen, Inc.) mixed with PBS (Gibco), and the tumor growth rate is monitored.

    Incubation:

    Article Title: Biomineralized outer membrane vesicles for synergistic immuno-photodynamic therapy of oral squamous cell carcinoma
    Article Snippet: .. First, OMVs containing 1 mg of total protein were dispersed in 1 mL of PBS (Gibco) and incubated overnight in a constant-temperature shaking incubator (200 rpm) at 37 °C to reach equilibrium. ..

    Article Title: Compound design of a patient-derived 3D cell culture system modelling early peritoneal endometriosis
    Article Snippet: Cells were permeabilised with 0.25% (v/v) Triton X-100 (Thermo Fisher Scientific, 85111) in PBS for 10 min at RT and blocked with 2% (w/v) bovine serum albumin (BSA; Sigma-Aldrich, A3803) for 1 h at RT. .. Cells were incubated with primary antibodies overnight at 4°C , followed by three 15 min PBS washes and incubation with secondary antibodies AlexaFluorTM 488 goat-anti-mouse IgG1 (Invitrogen, A21121) and AlexaFluorTM 568 goat-anti-rabbit (Invitrogen, A11011) at 1:1000 dilution, and DAPI (Sigma-Aldrich, D9542) in a 1:500 dilution, for 1 h at RT. .. The slides were mounted using FluoromountTM (Invitrogen, 00-4958-02).

    Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
    Article Snippet: Next, the cells were permeabilized with 0.5 % Triton X-100 (Merck) dissolved in PBS for 10 min and blocked with 3 % (w/v) bovine serum albumin (Merck) in PBS for 30 min and then with 5 % (v/v) goat serum (Fisher Scientific) dissolved in PBS for 30 min. Next, cells were incubated with a primary antibody using mouse monoclonal anti α-smooth muscle actin diluted in PBS (1:600; Sigma: A5228) overnight at 4 °C. .. The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMaskTM orange (1:1000; ThermoFisher) for 10 min at room temperature.

    Staining:

    Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
    Article Snippet: The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMaskTM orange (1:1000; ThermoFisher) for 10 min at room temperature. .. Afterward, cells were washed with PBS 3 times and stained with DAPI (Sigma Aldrich; 1:500) for 15 min. After staining, all the surfaces were washed three times with PBS after which they were mounted onto a glass slide using Mowiol (Sigma).

    Membrane:

    Article Title: Immunomodulatory topographies regulate myofibroblast differentiation and influence fibrous encapsulation of glaucoma drainage devices
    Article Snippet: The next day, the cells were washed 3 times with PBS and then incubated with a secondary antibody goat anti-mouse Alexa Flour 488 diluted in PBS (1:500; Molecular probes: A21121) and incubated in the dark for 1 h at room temperature. .. For the α-SMA screen, cells were washed three times with PBS and stained with phalloidin-TRITC diluted in PBS (1:200, ThermoFisher) for 45 min and washed 3 times again with PBS and stained with 4′,6-Diamidino-2-Phenylindole (DAPI) (Sigma Aldrich; 1:500) for 15 min. For the macrophage screen, the cell membrane was stained using CellMaskTM orange (1:1000; ThermoFisher) for 10 min at room temperature. .. Afterward, cells were washed with PBS 3 times and stained with DAPI (Sigma Aldrich; 1:500) for 15 min. After staining, all the surfaces were washed three times with PBS after which they were mounted onto a glass slide using Mowiol (Sigma).

    Sequencing:

    Article Title: Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data
    Article Snippet: Both cell lines were authenticated by STR profiling at ATCC ( https://www.atcc.org/ , last accessed 27 February 2026). .. Cells for sequencing were harvested with 0.25% Trypsin–ethylenediaminetetraacetic acid (EDTA) (Thermo Fisher, Cat. No. 25200072), washed with 1× PBS (pH 7.4; Thermo Fisher, Cat. No. 10010023), counted on a CountessTM II FL Automated Cell Counter (Thermo Fisher, Cat. No. AMQAF1000), and used as input for NEB Monarch HMW genomic DNA (gDNA) isolation, Hi-C crosslinking, RNeasy Plus Mini isolation, or frozen as dry pellets and stored at −80°C for use in Oxford Nanopore Technologies (ONT) Ultra-Long (UL) library preparations. .. Estimated cumulative population doubling level (PDL) calculations were performed using PDL = 3.32 (logXe-logXb) + S where log is the base 10 logarithm, Xb is the cell number at the beginning of the incubation period, Xe is the cell number at the end of the incubation period, and S is the starting PDL (ref ATCC Animal Cell Culture Guide ACCG-042024-v08, p6).

    Isolation:

    Article Title: Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data
    Article Snippet: Both cell lines were authenticated by STR profiling at ATCC ( https://www.atcc.org/ , last accessed 27 February 2026). .. Cells for sequencing were harvested with 0.25% Trypsin–ethylenediaminetetraacetic acid (EDTA) (Thermo Fisher, Cat. No. 25200072), washed with 1× PBS (pH 7.4; Thermo Fisher, Cat. No. 10010023), counted on a CountessTM II FL Automated Cell Counter (Thermo Fisher, Cat. No. AMQAF1000), and used as input for NEB Monarch HMW genomic DNA (gDNA) isolation, Hi-C crosslinking, RNeasy Plus Mini isolation, or frozen as dry pellets and stored at −80°C for use in Oxford Nanopore Technologies (ONT) Ultra-Long (UL) library preparations. .. Estimated cumulative population doubling level (PDL) calculations were performed using PDL = 3.32 (logXe-logXb) + S where log is the base 10 logarithm, Xb is the cell number at the beginning of the incubation period, Xe is the cell number at the end of the incubation period, and S is the starting PDL (ref ATCC Animal Cell Culture Guide ACCG-042024-v08, p6).

    Hi-C:

    Article Title: Haplotype-resolved genome assemblies of BJ and IMR-90 human fibroblast cell lines reveal extensive structural variation and enable reanalysis of historical sequencing data
    Article Snippet: Both cell lines were authenticated by STR profiling at ATCC ( https://www.atcc.org/ , last accessed 27 February 2026). .. Cells for sequencing were harvested with 0.25% Trypsin–ethylenediaminetetraacetic acid (EDTA) (Thermo Fisher, Cat. No. 25200072), washed with 1× PBS (pH 7.4; Thermo Fisher, Cat. No. 10010023), counted on a CountessTM II FL Automated Cell Counter (Thermo Fisher, Cat. No. AMQAF1000), and used as input for NEB Monarch HMW genomic DNA (gDNA) isolation, Hi-C crosslinking, RNeasy Plus Mini isolation, or frozen as dry pellets and stored at −80°C for use in Oxford Nanopore Technologies (ONT) Ultra-Long (UL) library preparations. .. Estimated cumulative population doubling level (PDL) calculations were performed using PDL = 3.32 (logXe-logXb) + S where log is the base 10 logarithm, Xb is the cell number at the beginning of the incubation period, Xe is the cell number at the end of the incubation period, and S is the starting PDL (ref ATCC Animal Cell Culture Guide ACCG-042024-v08, p6).



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    The consistency of YAP and LRP1 in tissue <t>microarray</t> specimen. ( a , b ) <t>TMA</t> slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.
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    Shanghai Biochip Co. Ltd tissue microarray analysis (tma) slides
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    Image Search Results


    The consistency of YAP and LRP1 in tissue microarray specimen. ( a , b ) TMA slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.

    Journal: Scientific Reports

    Article Title: Yes-Associated Protein (YAP) Promotes Tumorigenesis in Melanoma Cells Through Stimulation of Low-Density Lipoprotein Receptor-Related Protein 1 (LRP1)

    doi: 10.1038/s41598-017-14764-4

    Figure Lengend Snippet: The consistency of YAP and LRP1 in tissue microarray specimen. ( a , b ) TMA slides include forty skin melanoma tissues and eight skin normal tissues which locate on the bottom of the each TMA. Representative images of IHC from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( c ) Representative images of IHC from skin melanoma HCC TMA stained with anti-YAP or anti-LRP1 antibodies. Scale bar, 100 μM. ( d ) The statistical figure of skin melanoma IHC images from HCC TMA stained with anti-YAP or anti-LRP1 antibodies. The TMA data were analyzed using the χ2 test.

    Article Snippet: For IHC, melanoma tissue microarray analysis (TMA) slides were purchased from Biomax (Rockville, MD, USA).

    Techniques: Microarray, Staining