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vectashield mounting medium  (Vector Laboratories)


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    Structured Review

    Vector Laboratories vectashield mounting medium
    Vectashield Mounting Medium, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 22145 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vectashield+medium+with+dapi/VECTASHIELD+Antifade+Mounting+Medium+with+DAPI/pm42898335-91-74-77
    Average 98 stars, based on 22145 article reviews
    vectashield mounting medium - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    other:

    Article Title: Description of the Seminiferous Epithelium Cycle Stages in the Zebra Finch Taeniopygia guttata .
    Article Snippet: Following post-hybridization washes, slides were mounted in Vectashield medium with DAPI (Vector Laboratories, Newark, CA, USA, cat# H-1200-10).

    Incubation:

    Article Title: TBXA2R activates ERMs to drive motility, invasion, and metastatic colonization of TNBC cells
    Article Snippet: Cells were then washed with PBS and fixed with 10% trichloroacetic acid (#T0699; Sigma-Aldrich) for 10 min at room temperature, followed by extensive washes with TBS (20 mM Tris–HCl, pH 7.5, 154 mM NaCl, 2 mM EGTA, 2 mM MgCl 2 ). .. Cells were then permeabilized with 0.02% saponin (#0163; Amresco) diluted in TBS supplemented with 2% BSA (#ALB001.250; BioShop) for 1 h. Cells were then incubated overnight with rabbit anti-p-ERM primary antibody (1:5,000; ) or anti-p-myosin II antibody (1:200, #3671; Cell Signaling Technology) followed by goat anti-rabbit Alexa Fluor 488–conjugated secondary antibody (1:200, #A11070; Invitrogen) for 1 h. Glass coverslips were finally mounted in Vectashield medium with DAPI (#H-1200; Vector Laboratories), and images were acquired using an LSM 700 confocal microscope (Zeiss) with a 63x objective. .. Migration experiments were performed using the Oris Cell Migration assay (Platypus Technologies) as the manufacturer prescribed.

    Article Title: TDP-43 pathology is linked to motor neuron loss but is independent of stress granules in vivo
    Article Snippet: TDP-43 aptamer (1/100, TDP-43 Apt CGGUGUUGCU with a 3’ Biotin-TEG modification, ATDBio, Southampton, UK) prepared in protein block was applied to the tissue and incubated for 3 h at 4 °C followed by incubation with 4% PFA overnight at 4 °C. .. Sections were incubated with primary and secondary antibodies (1/100 goat-anti biotin Ab6652, 1/200 A647 donkey anti-goat Ab150135) then washed and mounted with Vectashield medium with DAPI (Vector labs, H-1200). .. Images were acquired with a ZEISS AxioScan Z1 slide scanner at 20X magnification microscope at 20X magnification.

    Article Title: TBXA2R activates ERMs to drive motility, invasion, and metastatic colonization of TNBC cells.
    Article Snippet: Cells were then washed with PBS and fixed with 10% trichloroacetic acid (#T0699; Sigma-Aldrich) for 10 min at room temperature, followed by extensive washes with TBS (20 mM Tris–HCl, pH 7.5, 154 mM NaCl, 2 mM EGTA, 2 mM MgCl2). .. Cells were then permeabilized with 0.02% saponin (#0163; Amresco) diluted in TBS supplemented with 2% BSA (#ALB001.250; BioShop) for 1 h. Cells were then incubated overnight with rabbit anti-p-ERM primary antibody (1:5,000; Roubinet et al, 2011) or anti-p-myosin II antibody (1:200, #3671; Cell Signaling Technology) followed by goat anti-rabbit Alexa Fluor 488–conjugated secondary antibody (1:200, #A11070; Invitrogen) for 1 h. Glass coverslips were finally mounted in Vectashield medium with DAPI (#H-1200; Vector Laboratories), and images were acquired using an LSM 700 confocal microscope (Zeiss) with a 63x objective. .. Cell migration and invasion assay Migration experiments were performed using the Oris Cell Migration assay (Platypus Technologies) as the manufacturer prescribed.

    Microscopy:

    Article Title: TBXA2R activates ERMs to drive motility, invasion, and metastatic colonization of TNBC cells
    Article Snippet: Cells were then washed with PBS and fixed with 10% trichloroacetic acid (#T0699; Sigma-Aldrich) for 10 min at room temperature, followed by extensive washes with TBS (20 mM Tris–HCl, pH 7.5, 154 mM NaCl, 2 mM EGTA, 2 mM MgCl 2 ). .. Cells were then permeabilized with 0.02% saponin (#0163; Amresco) diluted in TBS supplemented with 2% BSA (#ALB001.250; BioShop) for 1 h. Cells were then incubated overnight with rabbit anti-p-ERM primary antibody (1:5,000; ) or anti-p-myosin II antibody (1:200, #3671; Cell Signaling Technology) followed by goat anti-rabbit Alexa Fluor 488–conjugated secondary antibody (1:200, #A11070; Invitrogen) for 1 h. Glass coverslips were finally mounted in Vectashield medium with DAPI (#H-1200; Vector Laboratories), and images were acquired using an LSM 700 confocal microscope (Zeiss) with a 63x objective. .. Migration experiments were performed using the Oris Cell Migration assay (Platypus Technologies) as the manufacturer prescribed.

    Article Title: Estrogen produced in the retina by brain aromatase plays a significant role in zebrafish eye development.
    Article Snippet: Aromatase is a key enzyme in estrogen biosynthesis, expressed in multiple tissues including the brain and retina.. In teleost fish, Aromatase B (AroB), encoded by cyp19a1b, is brainspecific and highly expressed during early development, suggesting a role in neurogenesis.. Here, we investigated the role of AroB in zebrafish eye development using morpholino (MO)-mediated knockdown.

    Article Title: TBXA2R activates ERMs to drive motility, invasion, and metastatic colonization of TNBC cells.
    Article Snippet: Cells were then washed with PBS and fixed with 10% trichloroacetic acid (#T0699; Sigma-Aldrich) for 10 min at room temperature, followed by extensive washes with TBS (20 mM Tris–HCl, pH 7.5, 154 mM NaCl, 2 mM EGTA, 2 mM MgCl2). .. Cells were then permeabilized with 0.02% saponin (#0163; Amresco) diluted in TBS supplemented with 2% BSA (#ALB001.250; BioShop) for 1 h. Cells were then incubated overnight with rabbit anti-p-ERM primary antibody (1:5,000; Roubinet et al, 2011) or anti-p-myosin II antibody (1:200, #3671; Cell Signaling Technology) followed by goat anti-rabbit Alexa Fluor 488–conjugated secondary antibody (1:200, #A11070; Invitrogen) for 1 h. Glass coverslips were finally mounted in Vectashield medium with DAPI (#H-1200; Vector Laboratories), and images were acquired using an LSM 700 confocal microscope (Zeiss) with a 63x objective. .. Cell migration and invasion assay Migration experiments were performed using the Oris Cell Migration assay (Platypus Technologies) as the manufacturer prescribed.

    Fluorescence:

    Article Title: Estrogen produced in the retina by brain aromatase plays a significant role in zebrafish eye development.
    Article Snippet: Aromatase is a key enzyme in estrogen biosynthesis, expressed in multiple tissues including the brain and retina.. In teleost fish, Aromatase B (AroB), encoded by cyp19a1b, is brainspecific and highly expressed during early development, suggesting a role in neurogenesis.. Here, we investigated the role of AroB in zebrafish eye development using morpholino (MO)-mediated knockdown.

    Staining:

    Article Title: Alzheimer's disease target and drug discovery by leveraging multiomics and electronic health data.
    Article Snippet: The sections were treated with 0.5% Triton X-100 for 30 min and blocked in 10% fetal bovine serum (FBS) for 1 h. For organoid sections, anti-amyloid (B-4) Alexa Fluor 488 conjugated antibody (1:200; Santa Cruz Biotechnology; sc-28365) and anti-tau (phospho T205) Alexa Fluor 647 conjugated antibody (1:200; Abcam; AB307376) were used to detect amyloid-β and phosphorylated tau, respectively. .. Antibodies were stained for 2 h at room temperature and washed three times with phosphate-buffered saline (PBS) (20 min each) before mounting in Vectashield medium with DAPI (Vector Laboratories). ..

    Saline:

    Article Title: Alzheimer's disease target and drug discovery by leveraging multiomics and electronic health data.
    Article Snippet: The sections were treated with 0.5% Triton X-100 for 30 min and blocked in 10% fetal bovine serum (FBS) for 1 h. For organoid sections, anti-amyloid (B-4) Alexa Fluor 488 conjugated antibody (1:200; Santa Cruz Biotechnology; sc-28365) and anti-tau (phospho T205) Alexa Fluor 647 conjugated antibody (1:200; Abcam; AB307376) were used to detect amyloid-β and phosphorylated tau, respectively. .. Antibodies were stained for 2 h at room temperature and washed three times with phosphate-buffered saline (PBS) (20 min each) before mounting in Vectashield medium with DAPI (Vector Laboratories). ..



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    Characterization of morphology, size, and shape distribution of differentiated 3D enteroids in suspension (A) Representative micrographs of AO enteroids: bright-field microscopy shows live enteroids in suspension (left), scanning electron microscopy (SEM) reveals a dense microvillar surface (middle), and transmission electron microscopy (TEM) shows the organized microvilli-rich brush border, tight junctions (TJ), and glycocalyx (right). High-magnification brightfield and SEM images (bottom row) correspond to the areas outlined by dotted squares in the upper row. (B) Representative micrographs of BO enteroids: live bright-field microscopy illustrates typical basal-out morphology (left), SEM shows the smooth basal surface (middle), and TEM reveals the microvilli-rich brush border on the lumen-facing apical surface, confirming basal-out polarity (right). High-magnification views (bottom row) correspond to the areas outlined in the upper row. (C) Circularity analysis of AO ( n = 118) and BO enteroids ( n = 94) in suspension from brightfield micrographs. (D) Total cross-sectional surface area at 6 days of suspension culture for AO ( n = 122) and BO ( n = 94) enteroids. (E) Concentrations of Matrigel proteins (% of protein over total acquired protein) present in AO and BO enteroids in suspension cultures after washing. Data from different donors ( n = 4, Hu22-2jej, Hu22-3jej, Hu22-5jej, and Hu18-9jej) are shown as means +SD. (F) Representative confocal images following staining of zonula occludens-1 (ZO-1, green), phalloidin (F-actin; magenta) and nuclei <t>(DAPI;</t> blue), highlighting the continuous monolayer barrier in AO and BO enteroids. Scale bars, 20 μm. (G) Quantification of apical-out and basal-out polarity in enteroid suspensions by confocal microscopy ( n = 100 per population). (A–D, F–G). Donor Hu18-9jej was used throughout. See also ; and .
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    Characterization of morphology, size, and shape distribution of differentiated 3D enteroids in suspension (A) Representative micrographs of AO enteroids: bright-field microscopy shows live enteroids in suspension (left), scanning electron microscopy (SEM) reveals a dense microvillar surface (middle), and transmission electron microscopy (TEM) shows the organized microvilli-rich brush border, tight junctions (TJ), and glycocalyx (right). High-magnification brightfield and SEM images (bottom row) correspond to the areas outlined by dotted squares in the upper row. (B) Representative micrographs of BO enteroids: live bright-field microscopy illustrates typical basal-out morphology (left), SEM shows the smooth basal surface (middle), and TEM reveals the microvilli-rich brush border on the lumen-facing apical surface, confirming basal-out polarity (right). High-magnification views (bottom row) correspond to the areas outlined in the upper row. (C) Circularity analysis of AO ( n = 118) and BO enteroids ( n = 94) in suspension from brightfield micrographs. (D) Total cross-sectional surface area at 6 days of suspension culture for AO ( n = 122) and BO ( n = 94) enteroids. (E) Concentrations of Matrigel proteins (% of protein over total acquired protein) present in AO and BO enteroids in suspension cultures after washing. Data from different donors ( n = 4, Hu22-2jej, Hu22-3jej, Hu22-5jej, and Hu18-9jej) are shown as means +SD. (F) Representative confocal images following staining of zonula occludens-1 (ZO-1, green), phalloidin (F-actin; magenta) and nuclei <t>(DAPI;</t> blue), highlighting the continuous monolayer barrier in AO and BO enteroids. Scale bars, 20 μm. (G) Quantification of apical-out and basal-out polarity in enteroid suspensions by confocal microscopy ( n = 100 per population). (A–D, F–G). Donor Hu18-9jej was used throughout. See also ; and .
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    Characterization of morphology, size, and shape distribution of differentiated 3D enteroids in suspension (A) Representative micrographs of AO enteroids: bright-field microscopy shows live enteroids in suspension (left), scanning electron microscopy (SEM) reveals a dense microvillar surface (middle), and transmission electron microscopy (TEM) shows the organized microvilli-rich brush border, tight junctions (TJ), and glycocalyx (right). High-magnification brightfield and SEM images (bottom row) correspond to the areas outlined by dotted squares in the upper row. (B) Representative micrographs of BO enteroids: live bright-field microscopy illustrates typical basal-out morphology (left), SEM shows the smooth basal surface (middle), and TEM reveals the microvilli-rich brush border on the lumen-facing apical surface, confirming basal-out polarity (right). High-magnification views (bottom row) correspond to the areas outlined in the upper row. (C) Circularity analysis of AO ( n = 118) and BO enteroids ( n = 94) in suspension from brightfield micrographs. (D) Total cross-sectional surface area at 6 days of suspension culture for AO ( n = 122) and BO ( n = 94) enteroids. (E) Concentrations of Matrigel proteins (% of protein over total acquired protein) present in AO and BO enteroids in suspension cultures after washing. Data from different donors ( n = 4, Hu22-2jej, Hu22-3jej, Hu22-5jej, and Hu18-9jej) are shown as means +SD. (F) Representative confocal images following staining of zonula occludens-1 (ZO-1, green), phalloidin (F-actin; magenta) and nuclei (DAPI; blue), highlighting the continuous monolayer barrier in AO and BO enteroids. Scale bars, 20 μm. (G) Quantification of apical-out and basal-out polarity in enteroid suspensions by confocal microscopy ( n = 100 per population). (A–D, F–G). Donor Hu18-9jej was used throughout. See also ; and .

    Journal: iScience

    Article Title: Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine

    doi: 10.1016/j.isci.2026.117654

    Figure Lengend Snippet: Characterization of morphology, size, and shape distribution of differentiated 3D enteroids in suspension (A) Representative micrographs of AO enteroids: bright-field microscopy shows live enteroids in suspension (left), scanning electron microscopy (SEM) reveals a dense microvillar surface (middle), and transmission electron microscopy (TEM) shows the organized microvilli-rich brush border, tight junctions (TJ), and glycocalyx (right). High-magnification brightfield and SEM images (bottom row) correspond to the areas outlined by dotted squares in the upper row. (B) Representative micrographs of BO enteroids: live bright-field microscopy illustrates typical basal-out morphology (left), SEM shows the smooth basal surface (middle), and TEM reveals the microvilli-rich brush border on the lumen-facing apical surface, confirming basal-out polarity (right). High-magnification views (bottom row) correspond to the areas outlined in the upper row. (C) Circularity analysis of AO ( n = 118) and BO enteroids ( n = 94) in suspension from brightfield micrographs. (D) Total cross-sectional surface area at 6 days of suspension culture for AO ( n = 122) and BO ( n = 94) enteroids. (E) Concentrations of Matrigel proteins (% of protein over total acquired protein) present in AO and BO enteroids in suspension cultures after washing. Data from different donors ( n = 4, Hu22-2jej, Hu22-3jej, Hu22-5jej, and Hu18-9jej) are shown as means +SD. (F) Representative confocal images following staining of zonula occludens-1 (ZO-1, green), phalloidin (F-actin; magenta) and nuclei (DAPI; blue), highlighting the continuous monolayer barrier in AO and BO enteroids. Scale bars, 20 μm. (G) Quantification of apical-out and basal-out polarity in enteroid suspensions by confocal microscopy ( n = 100 per population). (A–D, F–G). Donor Hu18-9jej was used throughout. See also ; and .

    Article Snippet: VECTASHIELD Vibrance Antifade Mounting Medium with DAPI , Vector Laboratories , Cat #: H-1800–10.

    Techniques: Morphology, Suspension, Microscopy, Scanning Electron Microscopy, Transmission Assay, Electron Microscopy, Brightfield, Analysis, Confocal, Staining

    Fatty acid transport in 3D enteroids in suspension (A) Representative confocal images following staining with DAPI (nuclei; blue), SLC27A4 (solute carrier family 27 member 4, green) and phalloidin (F-actin; magenta), highlighting the expression pattern of the fatty acid transport protein in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (B and C) AO and BO enteroids were incubated with fluorescent fatty acid analog C1-BODIPY-C12 for 10 min and imaged live using widefield fluorescence microscopy. The dashed square indicates the region shown at higher magnification. (B) C1-BODIPY-C12 accumulated in fluorescent lipid droplets in AO enteroids. Scale bars, 10 μm. (C) BO enteroids showed intraluminal accumulation of C1-BODIPY-C12. Scale bars, 20 μm. (D) AO enteroids (donor Hu18-9jej) were co-incubated with fluorescent fatty acid analog C1-BODIPY-C12 and LipidTOX-DR for 10 minto visualize lipid droplets. AO enteroids were imaged live using widefield fluorescence microscopy. The dashed square indicates the region shown at higher magnification. Scale bars, 20 μm; inset scale bars, 10 μm. (A–D) Enteroids from donor Hu18-9jej were used. See also .

    Journal: iScience

    Article Title: Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine

    doi: 10.1016/j.isci.2026.117654

    Figure Lengend Snippet: Fatty acid transport in 3D enteroids in suspension (A) Representative confocal images following staining with DAPI (nuclei; blue), SLC27A4 (solute carrier family 27 member 4, green) and phalloidin (F-actin; magenta), highlighting the expression pattern of the fatty acid transport protein in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (B and C) AO and BO enteroids were incubated with fluorescent fatty acid analog C1-BODIPY-C12 for 10 min and imaged live using widefield fluorescence microscopy. The dashed square indicates the region shown at higher magnification. (B) C1-BODIPY-C12 accumulated in fluorescent lipid droplets in AO enteroids. Scale bars, 10 μm. (C) BO enteroids showed intraluminal accumulation of C1-BODIPY-C12. Scale bars, 20 μm. (D) AO enteroids (donor Hu18-9jej) were co-incubated with fluorescent fatty acid analog C1-BODIPY-C12 and LipidTOX-DR for 10 minto visualize lipid droplets. AO enteroids were imaged live using widefield fluorescence microscopy. The dashed square indicates the region shown at higher magnification. Scale bars, 20 μm; inset scale bars, 10 μm. (A–D) Enteroids from donor Hu18-9jej were used. See also .

    Article Snippet: VECTASHIELD Vibrance Antifade Mounting Medium with DAPI , Vector Laboratories , Cat #: H-1800–10.

    Techniques: Suspension, Confocal, Staining, Expressing, Incubation, Widefield, Fluorescence, Microscopy

    BCRP expression, localization and activity in AO enteroids in suspension (A) Schematic illustrating BCRP efflux under physiological function, inhibition or absence (e.g., knockout). (B) Representative confocal images following staining with DAPI (nuclei; blue), BCRP (green) and phalloidin (F-actin; magenta), highlighting the expression pattern of the BCRP transporter in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (C) BCRP efflux in AO enteroids (donor Hu18-9jej) calculated by PhA accumulation; transporter substrate: PhA, transporter inhibitor: KO143. Results plotted as mean ± SD. Data are shown as triplicates in three independent experiments; data points of each independent experiment denoted as an individual shape.

    Journal: iScience

    Article Title: Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine

    doi: 10.1016/j.isci.2026.117654

    Figure Lengend Snippet: BCRP expression, localization and activity in AO enteroids in suspension (A) Schematic illustrating BCRP efflux under physiological function, inhibition or absence (e.g., knockout). (B) Representative confocal images following staining with DAPI (nuclei; blue), BCRP (green) and phalloidin (F-actin; magenta), highlighting the expression pattern of the BCRP transporter in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (C) BCRP efflux in AO enteroids (donor Hu18-9jej) calculated by PhA accumulation; transporter substrate: PhA, transporter inhibitor: KO143. Results plotted as mean ± SD. Data are shown as triplicates in three independent experiments; data points of each independent experiment denoted as an individual shape.

    Article Snippet: VECTASHIELD Vibrance Antifade Mounting Medium with DAPI , Vector Laboratories , Cat #: H-1800–10.

    Techniques: Expressing, Activity Assay, Suspension, Inhibition, Knock-Out, Confocal, Staining

    CYP3A4 metabolic activity in AO enteroids in suspension and PBPK simulation (A) Representative confocal images following staining with DAPI (nuclei; blue), CYP3A4 (green), and phalloidin (F-actin; magenta), highlighting the expression pattern of the CYP3A4 metabolic enzyme in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (B) CYP3A4 metabolic activity in AO enteroids (donor Hu18-9jej) over a time period of 120 min. The concentration of the enzyme substrate terfenadine was monitored over time, as well as the formation of its metabolite fexofenadine. Data are shown as mean ± SD. (C) Intrinsic clearance of terfenadine in AO enteroids (donor: Hu18-9jej) and primary enterocytes (donors: Hu22-32jej, Hu23-1jej and Hu23-5jej). Data are shown as median ± IQR, ∗∗∗ p < 0.001 (Mann-Whitney U test). (D) Corrected intrinsic clearance of terfenadine considering the differences in CYP3A4 protein expression in AO enteroids (donor Hu18-9jej) and primary enterocytes (donors: Hu22-32jej, Hu23-1jej and Hu23-5jej. Data are shown as median ± IQR. Mann-Whitney U test showed no statistically significant difference between groups. (E) Simulated mean pharmacokinetics profile of a 60 mg dose of terfenadine in 140 virtual males (20–50 years, black line) with its 5th and 95th percentile profile shown as dashed lines. The green line represents the PBPK model mean prediction for AO enteroids (log concentration). The orange dots depict mean observed data from Okerholm et al. See also ; .

    Journal: iScience

    Article Title: Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine

    doi: 10.1016/j.isci.2026.117654

    Figure Lengend Snippet: CYP3A4 metabolic activity in AO enteroids in suspension and PBPK simulation (A) Representative confocal images following staining with DAPI (nuclei; blue), CYP3A4 (green), and phalloidin (F-actin; magenta), highlighting the expression pattern of the CYP3A4 metabolic enzyme in AO enteroids (donor Hu18-9jej). Scale bars, 20 μm. (B) CYP3A4 metabolic activity in AO enteroids (donor Hu18-9jej) over a time period of 120 min. The concentration of the enzyme substrate terfenadine was monitored over time, as well as the formation of its metabolite fexofenadine. Data are shown as mean ± SD. (C) Intrinsic clearance of terfenadine in AO enteroids (donor: Hu18-9jej) and primary enterocytes (donors: Hu22-32jej, Hu23-1jej and Hu23-5jej). Data are shown as median ± IQR, ∗∗∗ p < 0.001 (Mann-Whitney U test). (D) Corrected intrinsic clearance of terfenadine considering the differences in CYP3A4 protein expression in AO enteroids (donor Hu18-9jej) and primary enterocytes (donors: Hu22-32jej, Hu23-1jej and Hu23-5jej. Data are shown as median ± IQR. Mann-Whitney U test showed no statistically significant difference between groups. (E) Simulated mean pharmacokinetics profile of a 60 mg dose of terfenadine in 140 virtual males (20–50 years, black line) with its 5th and 95th percentile profile shown as dashed lines. The green line represents the PBPK model mean prediction for AO enteroids (log concentration). The orange dots depict mean observed data from Okerholm et al. See also ; .

    Article Snippet: VECTASHIELD Vibrance Antifade Mounting Medium with DAPI , Vector Laboratories , Cat #: H-1800–10.

    Techniques: Activity Assay, Suspension, Confocal, Staining, Expressing, Concentration Assay, MANN-WHITNEY, Drug discovery

    Journal: iScience

    Article Title: Proteomic and functional profiling of suspended jejunal enteroids reveals pharmacokinetic fidelity to native intestine

    doi: 10.1016/j.isci.2026.117654

    Figure Lengend Snippet:

    Article Snippet: VECTASHIELD Vibrance Antifade Mounting Medium with DAPI , Vector Laboratories , Cat #: H-1800–10.

    Techniques: Tissue, Recombinant, Membrane, Gentle, Cell Recovery, Staining, Plasmid Preparation, Saline, Viability Assay, Lysis, Mass Spectrometry, Software