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fluorescent dye dylighttm 649 conjugated to donkey anti-human igg (h+ l chains)  (Jackson Immuno)


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    Jackson Immuno fluorescent dye dylighttm 649 conjugated to donkey anti-human igg (h+ l chains)
    Fluorescent Dye Dylighttm 649 Conjugated To Donkey Anti Human Igg (H+ L Chains), supplied by Jackson Immuno, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/dylighttm+649/fluorescent+dye+dylighttm+649+conjugated+to+donkey+anti+human+igg++h++l+chains+/pm40615491-213-23-35
    Average 90 stars, based on 1 article reviews
    fluorescent dye dylighttm 649 conjugated to donkey anti-human igg (h+ l chains) - by Bioz Stars, 2026-09
    90/100 stars

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    Article Title: Adenosine is released during thalamic oscillations to provide negative feedback control.
    Article Snippet: .. Secondary antibodies were all raised in donkey, and conjugated to either Alexa FluorTM 488 (Invitrogen, Eugene, OR, USA), indocarbocyanine (CyTM3) or DyLightTM 549, or DyLightTM 649 (Jackson Immunoresearch, West Grove, PA, USA), for 2 h. Sections were then washed three times for 10 min periods in TBS-Tx to remove unbound antibodies, mounted on glass microscope slides, air dried, and sealed with glass coverslips using VectashieldTM antifade mounting medium (Vector Laboratories). ..

    Article Title: Diosmetin triggers cell apoptosis by activation of the p53/Bcl-2 pathway and inactivation of the Notch3/NF-κB pathway in HepG2 cells
    Article Snippet: Next, the cells were incubated with primary antibodies against p53 (#2527) and Notch3 (#5276) [1:500 dilution with 5% bovine serum albumin (BSA) in PBS; Cell Signaling Technology, Inc.] at 4°C overnight upon blocking the cells with 5% BSA dilution in PBS. .. DyLightTM 649-conjugated secondary antibodies (#009-490-006; Jackson ImmunoResearch Laboratories, Inc., West Grove, PA, USA) were applied at a dilution of 1:500 at room temperature for 1 h. The specimens were monitored using a TCP SP5 laser microscope (Leica Microsystems GmbH, Wetzlar, Germany). .. A specific small hairpin (sh)RNA targeting the Notch3 gene and a control shRNA (synthesized by Sangon Biotech Co., Ltd., Shanghai, China) were constructed into lenti-shRNA vectors, which were purchased from (GeneChem Co., Ltd., Shanghai, China).

    Article Title: Specific Dystrophins Selectively Associate with Inhibitory and Excitatory Synapses of the Mouse Cerebellum and their Loss Alters Expression of P2X7 Purinoceptors and Pro-Inflammatory Mediators
    Article Snippet: .. Secondary antibodies were all raised in donkey and conjugated to either Alexa FluorTM 488 (Invitrogen, Eugene, OR, USA), indocarbocyanine (Cy TM 3) or DyLightTM 549, or DyLightTM 649 (Jackson Immunoresearch, West Grove, PA, USA), for 2 h. Sections were then washed three times for 10-min periods in TBS-Tx to remove unbound antibodies, mounted on glass microscope slides, air dried, and sealed with glass coverslips using VectashieldTM antifade mounting medium (Vector Laboratories). ..



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    Image Search Results


    Design and development of a biomimetic nano-platform for live-cell fluorescence microscopy mimicking microvilli presentation of ligands for immune cells Chemical surface functionalization introduces reversible imine linkage for thermodynamic binding of (nano)particles, which is fixed by mild reduction. Biotin is covalently linked to the nanoparticle and binds to tetravalent streptavidin. Free binding sites are used by biotinylated ligands (e.g., antibodies) for stimulation of imaged cells.

    Journal: iScience

    Article Title: Cell surface morphology mimicking nano-bio platform for immune cell stimulation

    doi: 10.1016/j.isci.2024.111033

    Figure Lengend Snippet: Design and development of a biomimetic nano-platform for live-cell fluorescence microscopy mimicking microvilli presentation of ligands for immune cells Chemical surface functionalization introduces reversible imine linkage for thermodynamic binding of (nano)particles, which is fixed by mild reduction. Biotin is covalently linked to the nanoparticle and binds to tetravalent streptavidin. Free binding sites are used by biotinylated ligands (e.g., antibodies) for stimulation of imaged cells.

    Article Snippet: Ammonium hydroxide (NH 4 OH), Ethanol (EtOH, UV grade), 3-aminopropyltriethoxysilane (APTES), Acetonitrile (ACN, UV grade), sodium cyanoborohydride (NaBH 3 CN) (Penta Chemicals, Czech Republic), hydrogen Peroxide (H 2 O 2 ) (Lach:ner, Czech Republic), molecule 1 (4-(bromomethyl)benzaldehyde) was purchased and used without further purification (Merck) Polybead® amino microspheres, 0.112 μm (Polysciences, Inc., Germany), QdotTM 525 ITKTM Amino (PEG) quantum dots, sulfo-NHS-biotin, streptavidin, DylightTM Fluor 649 streptavidin, Alexa Fluor 647 goat anti-mouse IgG2A (Y2a) (Thermo Fisher Scientific, USA), anti-Hu CD3 biotin (MEM-57, Exbio, Czech Republic), were purchased and used as received without further purification.

    Techniques: Fluorescence, Microscopy, Binding Assay

    Fluorescent microscope images of nano-bio platform containing QDs and PS beads (A–D) Visualization of QDs (A and C) and PS beads (B and D) on functionalized nano-bio platform by fluorescence imaging: (A) and (B) represents binding of Alexa Fluor 647-labeled streptavidin (see for details); (C) and (D) represents binding of anti-Hu CD3ε biotin (mouse IgG) via non-labeled streptavidin and visualized by goat anti-mouse IgG Alexa Fluor 647-labelled secondary antibody. Scale bar in all images, 1 μm. See also <xref ref-type=Figures S3 and . " width="100%" height="100%">

    Journal: iScience

    Article Title: Cell surface morphology mimicking nano-bio platform for immune cell stimulation

    doi: 10.1016/j.isci.2024.111033

    Figure Lengend Snippet: Fluorescent microscope images of nano-bio platform containing QDs and PS beads (A–D) Visualization of QDs (A and C) and PS beads (B and D) on functionalized nano-bio platform by fluorescence imaging: (A) and (B) represents binding of Alexa Fluor 647-labeled streptavidin (see for details); (C) and (D) represents binding of anti-Hu CD3ε biotin (mouse IgG) via non-labeled streptavidin and visualized by goat anti-mouse IgG Alexa Fluor 647-labelled secondary antibody. Scale bar in all images, 1 μm. See also Figures S3 and .

    Article Snippet: Ammonium hydroxide (NH 4 OH), Ethanol (EtOH, UV grade), 3-aminopropyltriethoxysilane (APTES), Acetonitrile (ACN, UV grade), sodium cyanoborohydride (NaBH 3 CN) (Penta Chemicals, Czech Republic), hydrogen Peroxide (H 2 O 2 ) (Lach:ner, Czech Republic), molecule 1 (4-(bromomethyl)benzaldehyde) was purchased and used without further purification (Merck) Polybead® amino microspheres, 0.112 μm (Polysciences, Inc., Germany), QdotTM 525 ITKTM Amino (PEG) quantum dots, sulfo-NHS-biotin, streptavidin, DylightTM Fluor 649 streptavidin, Alexa Fluor 647 goat anti-mouse IgG2A (Y2a) (Thermo Fisher Scientific, USA), anti-Hu CD3 biotin (MEM-57, Exbio, Czech Republic), were purchased and used as received without further purification.

    Techniques: Microscopy, Fluorescence, Imaging, Binding Assay, Labeling

    Journal: iScience

    Article Title: Cell surface morphology mimicking nano-bio platform for immune cell stimulation

    doi: 10.1016/j.isci.2024.111033

    Figure Lengend Snippet:

    Article Snippet: Ammonium hydroxide (NH 4 OH), Ethanol (EtOH, UV grade), 3-aminopropyltriethoxysilane (APTES), Acetonitrile (ACN, UV grade), sodium cyanoborohydride (NaBH 3 CN) (Penta Chemicals, Czech Republic), hydrogen Peroxide (H 2 O 2 ) (Lach:ner, Czech Republic), molecule 1 (4-(bromomethyl)benzaldehyde) was purchased and used without further purification (Merck) Polybead® amino microspheres, 0.112 μm (Polysciences, Inc., Germany), QdotTM 525 ITKTM Amino (PEG) quantum dots, sulfo-NHS-biotin, streptavidin, DylightTM Fluor 649 streptavidin, Alexa Fluor 647 goat anti-mouse IgG2A (Y2a) (Thermo Fisher Scientific, USA), anti-Hu CD3 biotin (MEM-57, Exbio, Czech Republic), were purchased and used as received without further purification.

    Techniques: Recombinant, Plasmid Preparation, Software, Variant Assay