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vector leboratories  (Vector Laboratories)


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    Structured Review

    Vector Laboratories vector leboratories
    Vector Leboratories, supplied by Vector Laboratories, used in various techniques. Bioz Stars score: 98/100, based on 21989 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/vectashield-dapi/VECTASHIELD+Antifade+Mounting+Medium+with+DAPI/pmc13127484-31-7-7
    Average 98 stars, based on 21989 article reviews
    vector leboratories - by Bioz Stars, 2026-10
    98/100 stars

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    Related Articles

    Evaporation:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Incubation:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Plasmid Preparation:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Modification:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Chloramphenicol Acetyltransferase Assay:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Microscopy:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    RNA sequencing:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Staining:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Expressing:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Gene Expression:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Labeling:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    cDNA Synthesis:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Transfection:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.

    Injection:

    Article Title: DVE-1 is a telomere-binding protein and links the NuRD complex to telomere regulation in C. elegans
    Article Snippet: on, worms were immediately rehydrated using 10 μL of PBS-T (0.1% Triton X-100) and incubated for at least 10 min to allow sufficient rehydration. Approximately 8 μL of DAPI-containing mounting medium (Vector Laboratories, #H-1200-10) was subsequently added, and a coverslip was applied. The samples were incubated at room temperature for 15 min before being sealed with nail polish to prevent drying.



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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