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cd9  (Cell Signaling Technology Inc)


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    Structured Review

    Cell Signaling Technology Inc cd9
    Cd9, supplied by Cell Signaling Technology Inc, used in various techniques. Bioz Stars score: 96/100, based on 368 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/rabbit+anti+cd9+antibody/CD9+Rabbit+mAb/pm42878785-100-4-7
    Average 96 stars, based on 368 article reviews
    cd9 - by Bioz Stars, 2026-10
    96/100 stars

    Images

    Related Articles

    Labeling:

    Article Title: Enhanced Delivery of Rose Bengal by Amino Acids Starvation and Exosomes Inhibition in Human Astrocytoma Cells to Potentiate Anticancer Photodynamic Therapy Effects
    Article Snippet: Size and concentrations (2000 events each) were finally determined using the qNano software provided by Izon Science (Izon Control Suite version 3.1). .. A rabbit anti-CD9 antibody (Cell Signaling, #13174), fluorescently conjugated using a DyLight488 labeling kit (Biorad), was used to stain EVs. ..

    Article Title: Enhanced Delivery of Rose Bengal by Amino Acids Starvation and Exosomes Inhibition in Human Astrocytoma Cells to Potentiate Anticancer Photodynamic Therapy Effects.
    Article Snippet: Size and concentrations (2000 events each) were finally determined using the qNano software provided by Izon Science (Izon Control Suite version 3.1). .. A rabbit anti-CD9 antibody (Cell Signaling, #13174), fluorescently conjugated using a DyLight488 labeling kit (Biorad), was used to stain EVs. ..

    Article Title: Extracellular vesicles secreted by cumulus cells contain microRNAs that are potential regulatory factors of mouse oocyte developmental competence
    Article Snippet: The resulting pellet was resuspended in 50 μl of sterile ice-cold D-PBS or exosome-depleted α-MEM–Glutamax medium for EV or miRNA characterization, respectively (see below). .. EVs from FL-SN-CCs, FL-SN-CCs + DOs, FL-NSN-CCs, FL-NSN-CCs + DOs, or exosome-depleted α-MEM–Glutamax medium-only samples were labelled with a rabbit anti-CD9 antibody (Cell Signaling, #13174, Danvers, MA, USA), fluorescently conjugated with the DyLight488 labeling kit (BioRad, Hercules, CA, USA). ..

    Staining:

    Article Title: Enhanced Delivery of Rose Bengal by Amino Acids Starvation and Exosomes Inhibition in Human Astrocytoma Cells to Potentiate Anticancer Photodynamic Therapy Effects
    Article Snippet: Size and concentrations (2000 events each) were finally determined using the qNano software provided by Izon Science (Izon Control Suite version 3.1). .. A rabbit anti-CD9 antibody (Cell Signaling, #13174), fluorescently conjugated using a DyLight488 labeling kit (Biorad), was used to stain EVs. ..

    Article Title: Enhanced Delivery of Rose Bengal by Amino Acids Starvation and Exosomes Inhibition in Human Astrocytoma Cells to Potentiate Anticancer Photodynamic Therapy Effects.
    Article Snippet: Size and concentrations (2000 events each) were finally determined using the qNano software provided by Izon Science (Izon Control Suite version 3.1). .. A rabbit anti-CD9 antibody (Cell Signaling, #13174), fluorescently conjugated using a DyLight488 labeling kit (Biorad), was used to stain EVs. ..

    Western Blot:

    Article Title: ROS-responsive hydrogel-delivered miR-665 targets STAT3 to alleviate inflammation and promote hair follicle regeneration in alopecia areata
    Article Snippet: The exposure maps were analyzed by grayscale using ImageJ. .. The same method was used with a mouse anti-Alix antibody (1∶1000, CST), rabbit anti-CD9 antibody (1∶1000, CST), rabbit anti-CD63 antibody (1∶1000, CST), and mouse anti-TSG101 antibody (1∶1000, CST) for WB identification of EVs. ..

    Article Title: Role of tear exosomes in the spread of herpes simplex virus type 1 in recurrent herpes simplex keratitis.
    Article Snippet: BACKGROUND: Herpes simplex keratitis (HSK) is the most common but serious infectious keratitis with high recurrence.. It is predominantly caused by herpes simplex virus type 1 (HSV-1).. The spread mechanism of HSV-1 in HSK is not entirely clear.

    Article Title: ROS-responsive hydrogel-delivered miR-665 targets STAT3 to alleviate inflammation and promote hair follicle regeneration in alopecia areata.
    Article Snippet: The exposure maps were analyzed by grayscale using ImageJ. .. The same method was used with a mouse anti-Alix antibody (1∶1000, CST), rabbit anti-CD9 antibody (1∶1000, CST), rabbit antiCD63 antibody (1∶1000, CST), and mouse anti-TSG101 antibody (1∶1000, CST) for WB identification of EVs. ..



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    ABclonal Biotechnology cd9
    Preparation and characterization of functionalized P3-EVs@D + Q. ( A-B ) Schematic diagrams of construction of P3-EVs@D + Q and its sustained release of dasatinib and quercetin (abbreviated as D and Q, respectively). ( C ) Construction of the plasmid used for HEK293 cell transfection to obtain the EVs expressing P3 peptide. ( D ) Representative TEM images of EVs and P3-EVs. The parts marked by the dashed box are enlarged below the relevant original images. ( E ) DLS analysis of purified EVs and P3-EVs. ( F ) Surface zeta potential of the two different EVs. ( G ) Representative western blotting images and quantifications for canonical EV markers, including TSG101, CD63, CD81 and <t>CD9.</t> Calnexin served as a negative control marker and HEK293 cellular proteins served as the control sample. ( H ) Representative fluorescence images of inguinal adipose tissues after treatment with DiO-labelled EVs or P3-EVs via tail intravenous injection in mice (i, ii, and iii denote three independent biological replicates). ( I ) Representative TEM images of P3-EVs@D + Q. The part marked by the dashed box is enlarged below. ( J ) Surface zeta potential of P3-EVs@D + Q. ( K ) Sustained release curves of dasatinib or quercetin encapsulated in EVs or P3-EVs. EVs, extracellular vesicles
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    Image Search Results


    Preparation and characterization of functionalized P3-EVs@D + Q. ( A-B ) Schematic diagrams of construction of P3-EVs@D + Q and its sustained release of dasatinib and quercetin (abbreviated as D and Q, respectively). ( C ) Construction of the plasmid used for HEK293 cell transfection to obtain the EVs expressing P3 peptide. ( D ) Representative TEM images of EVs and P3-EVs. The parts marked by the dashed box are enlarged below the relevant original images. ( E ) DLS analysis of purified EVs and P3-EVs. ( F ) Surface zeta potential of the two different EVs. ( G ) Representative western blotting images and quantifications for canonical EV markers, including TSG101, CD63, CD81 and CD9. Calnexin served as a negative control marker and HEK293 cellular proteins served as the control sample. ( H ) Representative fluorescence images of inguinal adipose tissues after treatment with DiO-labelled EVs or P3-EVs via tail intravenous injection in mice (i, ii, and iii denote three independent biological replicates). ( I ) Representative TEM images of P3-EVs@D + Q. The part marked by the dashed box is enlarged below. ( J ) Surface zeta potential of P3-EVs@D + Q. ( K ) Sustained release curves of dasatinib or quercetin encapsulated in EVs or P3-EVs. EVs, extracellular vesicles

    Journal: Journal of Nanobiotechnology

    Article Title: Suppression of senescent metabolism of adipose tissue by rebalancing mitochondrial homeostasis via a selective drug delivery system

    doi: 10.1186/s12951-026-04594-w

    Figure Lengend Snippet: Preparation and characterization of functionalized P3-EVs@D + Q. ( A-B ) Schematic diagrams of construction of P3-EVs@D + Q and its sustained release of dasatinib and quercetin (abbreviated as D and Q, respectively). ( C ) Construction of the plasmid used for HEK293 cell transfection to obtain the EVs expressing P3 peptide. ( D ) Representative TEM images of EVs and P3-EVs. The parts marked by the dashed box are enlarged below the relevant original images. ( E ) DLS analysis of purified EVs and P3-EVs. ( F ) Surface zeta potential of the two different EVs. ( G ) Representative western blotting images and quantifications for canonical EV markers, including TSG101, CD63, CD81 and CD9. Calnexin served as a negative control marker and HEK293 cellular proteins served as the control sample. ( H ) Representative fluorescence images of inguinal adipose tissues after treatment with DiO-labelled EVs or P3-EVs via tail intravenous injection in mice (i, ii, and iii denote three independent biological replicates). ( I ) Representative TEM images of P3-EVs@D + Q. The part marked by the dashed box is enlarged below. ( J ) Surface zeta potential of P3-EVs@D + Q. ( K ) Sustained release curves of dasatinib or quercetin encapsulated in EVs or P3-EVs. EVs, extracellular vesicles

    Article Snippet: The antibodies used in this study include Calnexin (1:1000, A15631, ABclonal, China), CD63 (1:1000, A19023, ABclonal), CD9 (1:2000, A1703, ABclonal), CD81 (1:2000, A22983, ABclonal), TSG101 (1:1000, A2216, ABclonal), HA (1:10000, #2367, Cell Signaling Technology), p16 (1:1000, ab51243, Abcam, UK), p21 (1:1000, ab188224, Abcam), p62 (1:10000, ab109012, Abcam), LC3B (1:2000, 81004-1-RR, Proteintech, USA), and TOM20 (1:5000, 11802-1-AP, Proteintech).

    Techniques: Plasmid Preparation, Transfection, Expressing, Purification, Zeta Potential Analyzer, Western Blot, Negative Control, Marker, Control, Fluorescence, Injection