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autofluorescence  (Vector Laboratories)


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    Structured Review

    Vector Laboratories autofluorescence
    Autofluorescence, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 99/100, based on 904 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/trueview+autofluorescence+quenching+kit/Vector%C2%AE+TrueVIEW%C2%AE+Autofluorescence+Quenching+Kit/pmc12919959-231-1-4
    Average 99 stars, based on 904 article reviews
    autofluorescence - by Bioz Stars, 2026-09
    99/100 stars

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    Related Articles

    Blocking Assay:

    Article Title: Endothelial ACKR1 expression regulates neutrophil infiltration and breast cancer metastatic engraftment in the lung metastatic niche
    Article Snippet: .. The next day, sections were washed three times in PBS-T, treated with secondary antibodies (1:1000 in blocking buffer) for 1 hour at room temperature, and washed again in PBS-T. Quenching was performed with the Vector TrueVIEW Autofluorescence Quenching Kit (Vector Labs, SP-8400-15) per manufacturer’s instructions, and sections were mounted in VECTASHIELD Vibrance Antifade Mounting Medium with DAPI (Vector Labs, H-1800). ..

    Fluorescence:

    Article Title: Micro/nanoplastics induce thyroid follicular cell pyroptosis to trigger thyrotoxicity by activating NF-κB signaling.
    Article Snippet: .. Nonspecific fluorescence was quenched using Vector® TrueVIEW® Autofluorescence Quenching Kit. .. Fluorescent images were acquired using a fluorescence microscope (Carl Zeiss, Gottingen, Germany) with consistent exposure settings across all samples.

    Article Title: Micro/nanoplastics induce thyroid follicular cell pyroptosis to trigger thyrotoxicity by activating NF-κB signaling
    Article Snippet: .. Nonspecific fluorescence was quenched using Vector ® TrueVIEW ® Autofluorescence Quenching Kit. .. Fluorescent images were acquired using a fluorescence microscope (Carl Zeiss, Gottingen, Germany) with consistent exposure settings across all samples.

    Incubation:

    Article Title: HIF-1α + CD4 + T cells coordinate a tissue-resident immune cell network in the lung.
    Article Snippet: Lungs were washed in PBS, incubated in a 30% sucrose solution for 36 hours and embedded in OCT. For immunostaining of lung sections from Egln3-YFP mice, tissues were sectioned at 10-30 μm on a cryostat and incubated with 5% blocking buffer (Jackson ImmunoResearch) for 2 hours. .. Slides were incubated with indicated antibodies overnight at 4 ◦ C followed by washing with PBS, DAPI staining (2 μg/mL, Merck) and treatment with TrueView Autofluorescence Quenching Kit (Vector) to reduce autofluorescence. .. Sections were mounted using SlowFade Diamond Antifade Mountant (Thermo Fisher) to preserve Egln3-YFP fluorescence.

    Staining:

    Article Title: HIF-1α + CD4 + T cells coordinate a tissue-resident immune cell network in the lung.
    Article Snippet: Lungs were washed in PBS, incubated in a 30% sucrose solution for 36 hours and embedded in OCT. For immunostaining of lung sections from Egln3-YFP mice, tissues were sectioned at 10-30 μm on a cryostat and incubated with 5% blocking buffer (Jackson ImmunoResearch) for 2 hours. .. Slides were incubated with indicated antibodies overnight at 4 ◦ C followed by washing with PBS, DAPI staining (2 μg/mL, Merck) and treatment with TrueView Autofluorescence Quenching Kit (Vector) to reduce autofluorescence. .. Sections were mounted using SlowFade Diamond Antifade Mountant (Thermo Fisher) to preserve Egln3-YFP fluorescence.

    Article Title: The chromatin remodeling complex PRC2 safeguards cell fate in alveolar epithelial type 2 cells
    Article Snippet: Tissue sections were incubated with primary antibodies overnight at 4 degrees C followed by either a two-hour incubation at room temperature with fluorescently conjugated secondary antibodies or amplification using the ImmPRESS HRP Horse anti-Rabbit IgG Polymer Detection Kit (Vector Labs (MP-7401-50) and subsequent application of TSA fluorophores (Akoya Biosciences) (described in ). .. Autofluorescence was quenched using the Vector TrueVIEW Autofluorescence Quenching Kit (Vector, SP-8500-15), samples were stained with DAPI (Invitrogen, D1306), and coverslips were mounted onto slides with Prolong Gold antifade mounting medium (Invitrogen, P36930). .. Brightfield images were taken using a Nikon upright widefield microscope with 20X objective.



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    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei <t>(DAPI;</t> blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.
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    Image Search Results


    Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei (DAPI; blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.

    Journal: Journal of Translational Autoimmunity

    Article Title: T cell proliferative response to a homocitrullinated peptide correlates with joint pathology in collagen induced arthritis

    doi: 10.1016/j.jtauto.2025.100345

    Figure Lengend Snippet: Citrullinated and Homocitrullinated Proteins/Peptides are Present in DBA/1J Metatarsophalangeal Joints. A) Representative hematoxylin + eosin (H&E) at 80× magnification and immunofluorescent micrographs at 20× magnification of joints from DBA/1J mice immunized with bovine type II collagen (arthritic: N = 9; non-arthritic: N = 10) or PBS (N = 9). Scale bars represent 500 μm. Max projections of Z-stacks show nuclei (DAPI; blue), citrullinated proteins/peptides (CitP; green), and homocitrullinated proteins/peptides (HomoCitP; red). Corrected total fluorescence intensity for B) CitP and C) HomoCitP in three joint structures: bone marrow, synovium, and cartilage. Graphs show the median [IQR], with each symbol representing an individual mouse. Statistical analysis was performed using Kruskal-Wallis with Dunn's multiple comparisons test, and the resulting p-values were p = 0.0046, p = 0.0084, p = 0.4076, p = 0.0143, p = 0.0136, and p = 0.1733 respectively, with p-values for pairwise comparisons indicated on the graphs. ns: not significant.

    Article Snippet: Following application of TrueView autofluorescence quencher, slides were mounted using Vectashield Vibrance Antifade mounting media with DAPI (SP-8500-15; Vector Laboratories; USA) and air dried for 2 h before imaging on the Nikon Ti2-E microscope.

    Techniques: Fluorescence