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sterile disposable parallel flow chamber ibitreat - slide i luer  (ibidi GmbH)

 
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    ibidi GmbH sterile disposable parallel flow chamber ibitreat - slide i luer
    Schematic representation of devices used to perform ASC adhesion and detachment assays. The <t>parallel</t> <t>flow</t> <t>chamber</t> slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.
    Sterile Disposable Parallel Flow Chamber Ibitreat Slide I Luer, supplied by ibidi GmbH, 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/disposable+flow+chambers/sterile+disposable+parallel+flow+chamber+ibitreat+++slide+i+luer/pmc07214883-122-8-17
    Average 90 stars, based on 1 article reviews
    sterile disposable parallel flow chamber ibitreat - slide i luer - by Bioz Stars, 2026-09
    90/100 stars

    Images

    1) Product Images from "Adipose mesenchymal stromal/stem cells expanded by a GMP compatible protocol displayed improved adhesion on cancer cells in flow conditions"

    Article Title: Adipose mesenchymal stromal/stem cells expanded by a GMP compatible protocol displayed improved adhesion on cancer cells in flow conditions

    Journal: Annals of Translational Medicine

    doi: 10.21037/atm.2020.04.25

    Schematic representation of devices used to perform ASC adhesion and detachment assays. The parallel flow chamber slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.
    Figure Legend Snippet: Schematic representation of devices used to perform ASC adhesion and detachment assays. The parallel flow chamber slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.

    Techniques Used: Inverted Epifluorescence, Labeling



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    Schematic representation of devices used to perform ASC adhesion and detachment assays. The <t>parallel</t> <t>flow</t> <t>chamber</t> slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.
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    Schematic representation of devices used to perform ASC adhesion and detachment assays. The <t>parallel</t> <t>flow</t> <t>chamber</t> slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.
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    Image Search Results


    Schematic representation of devices used to perform ASC adhesion and detachment assays. The parallel flow chamber slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.

    Journal: Annals of Translational Medicine

    Article Title: Adipose mesenchymal stromal/stem cells expanded by a GMP compatible protocol displayed improved adhesion on cancer cells in flow conditions

    doi: 10.21037/atm.2020.04.25

    Figure Lengend Snippet: Schematic representation of devices used to perform ASC adhesion and detachment assays. The parallel flow chamber slide (see photographic enlargement), was placed on an inverted epifluorescence microscope. Washed ASC after fluorescent labeling were resuspended with perfusion medium in a conical tube (Reservoir). In controlled environment (37 °C; standard atmospheric pCO2 and humidity) ASC were perfused in the parallel flow chamber through a small bore catheter. Flow was imposed by a syringe pump (Harvard apparatus). Adherent and detaching ASC were visualized by a digital camera and the number of adherent cells was estimated by image analysis approach. Timing of flow rate regulation and of digital image capture was reported in methods section and in Figure 1A. Dashed arrows represent the direction of flowing medium containing labeled ASC. Dashed orange box encloses devices placed under controlled environmental conditions.

    Article Snippet: Experiments were performed taking advantage of a sterile disposable parallel flow chamber (ibiTreat - Slide I Luer, Ibidi GmbH, Gräfelfing, Germany).

    Techniques: Inverted Epifluorescence, Labeling