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qarray mini microarray spotter with 16 pins  (Genetix GmbH)

 
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    Genetix GmbH qarray mini microarray spotter with 16 pins
    Qarray Mini Microarray Spotter With 16 Pins, supplied by Genetix 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/microarray+spotter/qarray+mini+microarray+spotter+with+16+pins/pmc02669481-268-52-53
    Average 90 stars, based on 1 article reviews
    qarray mini microarray spotter with 16 pins - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    Concentration Assay:

    Article Title: Validation of candidate genes putatively associated with resistance to SCMV and MDMV in maize ( Zea mays L.) by expression profiling
    Article Snippet: .. Subsequently, pellets were dissolved in variable amounts of 50% dimethyl sulphoxide (DMSO) to the final concentration of 420 ng/μl and 5 μl of each sample was transferred into 384 well plates and spotted to Nexterion Slides A+ (SCHOTT JENA er GLAS GmbH, Jena, Germany) using the Qarray mini microarray spotter with 16 pins (Genetix GmbH, Munich, Germany). ..

    Microarray:

    Article Title: Validation of candidate genes putatively associated with resistance to SCMV and MDMV in maize ( Zea mays L.) by expression profiling
    Article Snippet: .. Subsequently, pellets were dissolved in variable amounts of 50% dimethyl sulphoxide (DMSO) to the final concentration of 420 ng/μl and 5 μl of each sample was transferred into 384 well plates and spotted to Nexterion Slides A+ (SCHOTT JENA er GLAS GmbH, Jena, Germany) using the Qarray mini microarray spotter with 16 pins (Genetix GmbH, Munich, Germany). ..



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    Image Search Results


    Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a microarray functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.

    Journal: Sensors and Actuators B: Chemical

    Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

    doi: 10.1016/j.snb.2024.136939

    Figure Lengend Snippet: Fig. 3. Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs (Rabbit IgG-Tag1, Rabbit IgG-Tag2 and Rabbit IgG-Tag3) immobilized on a microarray functionalized with streptavidin (printed at a concentration of 2 mg/mL) and released after incubation with biotin. Blue bars reflect the AAC immobilized on streptavidin, yellow bars represent the AAC left on the spots after biotin-mediated release. Mean ± standard deviation of three independent measurements.

    Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

    Techniques: Fluorescence, Labeling, Microarray, Concentration Assay, Incubation, Standard Deviation

    Fig. 4. Sequence-selective recapture on DNA microarray of 3 different AACs previously immobilized on streptavidin coated magnetic beads and released upon incubation with biotin. Bars represent the Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs. Mean ± standard deviation of three independent measurements.

    Journal: Sensors and Actuators B: Chemical

    Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

    doi: 10.1016/j.snb.2024.136939

    Figure Lengend Snippet: Fig. 4. Sequence-selective recapture on DNA microarray of 3 different AACs previously immobilized on streptavidin coated magnetic beads and released upon incubation with biotin. Bars represent the Relative Fluorescence Intensity measured on the spots after the interaction of fluorescently labeled secondary antibody with different AACs. Mean ± standard deviation of three independent measurements.

    Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

    Techniques: Sequencing, Microarray, Magnetic Beads, Incubation, Fluorescence, Labeling, Standard Deviation

    Fig. 5. Detection of EVs by label free interferometry separated and recaptured on DNA microarray using antiCD9-Tag2 (red bars). In the negative control, AAC- functionalized magnetic beads were incubated only with PBS-M (blue bars). Mean ± standard deviation of three independent measurements.

    Journal: Sensors and Actuators B: Chemical

    Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

    doi: 10.1016/j.snb.2024.136939

    Figure Lengend Snippet: Fig. 5. Detection of EVs by label free interferometry separated and recaptured on DNA microarray using antiCD9-Tag2 (red bars). In the negative control, AAC- functionalized magnetic beads were incubated only with PBS-M (blue bars). Mean ± standard deviation of three independent measurements.

    Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

    Techniques: Microarray, Negative Control, Magnetic Beads, Incubation, Standard Deviation

    Fig. 6. Schematic representation of recapture experiment on ExoView R100 (upper panel) and relative high resolution close ups of a Probe2 spot throughout experimental stages (bottom panel). From left to the right it can be seen i) the surface of the DNA spot, ii) label free interferometry picture of EVs captured on the same spot, and iii) red and green fluorescence picture of the same spot after incubation with labeled antibodies. The bar graphs represent label free interferometric and fluorescent detection of EVs on DNA microarray after separation using streptavidin coated magnetic beads: (b) functionalized with antiCD9-Tag2; (c) func- tionalized with Rabbit IgG-Tag2; (d) non functionalized with AACs. As additional negative control, detection of plasma added with antiCD9-Tag2 without previous separation of EVs on magnetic beads (e). Mean ± standard deviation of three independent measurements.

    Journal: Sensors and Actuators B: Chemical

    Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

    doi: 10.1016/j.snb.2024.136939

    Figure Lengend Snippet: Fig. 6. Schematic representation of recapture experiment on ExoView R100 (upper panel) and relative high resolution close ups of a Probe2 spot throughout experimental stages (bottom panel). From left to the right it can be seen i) the surface of the DNA spot, ii) label free interferometry picture of EVs captured on the same spot, and iii) red and green fluorescence picture of the same spot after incubation with labeled antibodies. The bar graphs represent label free interferometric and fluorescent detection of EVs on DNA microarray after separation using streptavidin coated magnetic beads: (b) functionalized with antiCD9-Tag2; (c) func- tionalized with Rabbit IgG-Tag2; (d) non functionalized with AACs. As additional negative control, detection of plasma added with antiCD9-Tag2 without previous separation of EVs on magnetic beads (e). Mean ± standard deviation of three independent measurements.

    Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

    Techniques: Fluorescence, Incubation, Labeling, Microarray, Magnetic Beads, Negative Control, Clinical Proteomics, Standard Deviation

    Fig. 8. Recapture and multiplexed detection on DNA microarray of EVs sepa- rated using antiCD9-Tag2 immobilized on magnetic beads and labeled using antiCD63-Tag1. Mean ± standard deviation of three independent measurements.

    Journal: Sensors and Actuators B: Chemical

    Article Title: Sequential separation and profiling of extracellular vesicles using antibody-aptamer conjugates

    doi: 10.1016/j.snb.2024.136939

    Figure Lengend Snippet: Fig. 8. Recapture and multiplexed detection on DNA microarray of EVs sepa- rated using antiCD9-Tag2 immobilized on magnetic beads and labeled using antiCD63-Tag1. Mean ± standard deviation of three independent measurements.

    Article Snippet: Supports were spotted using a noncontact microarray spotter (sciFLEXARRAYER S12, Scienion, Berlin) equipped with an 80 μm nozzle.

    Techniques: Microarray, Magnetic Beads, Labeling, Standard Deviation