fluorescence microarray scanner Search Results


fluorescent microarray scanner  (Tecan Systems)
90
Tecan Systems fluorescent microarray scanner
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Fluorescent Microarray Scanner, supplied by Tecan Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescent microarray scanner  (CapitalBio Corporation)
90
CapitalBio Corporation fluorescent microarray scanner
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Fluorescent Microarray Scanner, supplied by CapitalBio Corporation, 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/result/fluorescent microarray scanner/product/CapitalBio Corporation
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fluorescence microarray scanner  (VIDIA Inc)
90
VIDIA Inc fluorescence microarray scanner
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Fluorescence Microarray Scanner, supplied by VIDIA Inc, 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/result/fluorescence microarray scanner/product/VIDIA Inc
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fluorescence microarray scanner - by Bioz Stars, 2026-02
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genepix 4000b fluorescence microarray scanner  (CapitalBio Corporation)
90
CapitalBio Corporation genepix 4000b fluorescence microarray scanner
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Genepix 4000b Fluorescence Microarray Scanner, supplied by CapitalBio Corporation, 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/result/genepix 4000b fluorescence microarray scanner/product/CapitalBio Corporation
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fluorescence microarray laser scanner  (RayBiotech inc)
90
RayBiotech inc fluorescence microarray laser scanner
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Fluorescence Microarray Laser Scanner, supplied by RayBiotech inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescence microarray laser scanner - by Bioz Stars, 2026-02
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fluorescence microarray scanner ls reloadedtm  (Tecan Systems)
90
Tecan Systems fluorescence microarray scanner ls reloadedtm
Histogram comparing binding of hNCRD fusion proteins to the high-mannose <t>microarray.</t> Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.
Fluorescence Microarray Scanner Ls Reloadedtm, supplied by Tecan Systems, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescent microarray scanner arrayworx e-biochip reader  (Applied Precision Inc)
90
Applied Precision Inc fluorescent microarray scanner arrayworx e-biochip reader
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
Fluorescent Microarray Scanner Arrayworx E Biochip Reader, supplied by Applied Precision Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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microarray fluorescence reader typhoon trio+ microarray scanner  (Amersham Life Sciences Inc)
90
Amersham Life Sciences Inc microarray fluorescence reader typhoon trio+ microarray scanner
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
Microarray Fluorescence Reader Typhoon Trio+ Microarray Scanner, supplied by Amersham Life Sciences Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescence microarray laser scanner 60  (RayBiotech inc)
90
RayBiotech inc fluorescence microarray laser scanner 60
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
Fluorescence Microarray Laser Scanner 60, supplied by RayBiotech inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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fluorescence microarray laser scanner 60 - by Bioz Stars, 2026-02
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fluorescence microarray scanner  (Innopsys Inc)
90
Innopsys Inc fluorescence microarray scanner
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
Fluorescence Microarray Scanner, supplied by Innopsys Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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confocal fluorescent scanner luxscantm 10k microarray scanner  (CapitalBio Corporation)
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CapitalBio Corporation confocal fluorescent scanner luxscantm 10k microarray scanner
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
Confocal Fluorescent Scanner Luxscantm 10k Microarray Scanner, supplied by CapitalBio Corporation, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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10 39 /c 2s m 06 58 2g fluorescence microarray scanner  (Alpha Innotech)
90
Alpha Innotech 10 39 /c 2s m 06 58 2g fluorescence microarray scanner
a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA <t>microarray</t> scanner.
10 39 /C 2s M 06 58 2g Fluorescence Microarray Scanner, supplied by Alpha Innotech, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Histogram comparing binding of hNCRD fusion proteins to the high-mannose microarray. Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.

Journal:

Article Title: Recognition of Mannosylated Ligands and Influenza A Virus by Human SP-D: Contributions of an Extended Site and Residue 343 †

doi: 10.1021/bi8022703

Figure Lengend Snippet: Histogram comparing binding of hNCRD fusion proteins to the high-mannose microarray. Binding of hNCRD fusion proteins was assessed using PENTA-HIS Alexa Fluor 555 antibody conjugate as described in the Methods. Solid-phase carbohydrates are illustrated in Figure 1B. A selected experiment is shown.

Article Snippet: After two washes and centrifugation, slides were scanned with a fluorescent microarray scanner (Tecan).

Techniques: Binding Assay, Microarray

a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA microarray scanner.

Journal: PLoS ONE

Article Title: A Microfluidic Platform for High-Throughput Multiplexed Protein Quantitation

doi: 10.1371/journal.pone.0117744

Figure Lengend Snippet: a) microfluidic design: the device consists of two PDMS layers: flow (blue) and control (red). The chip is an array of eight rows by 48 columns for 384 unit cells. Each unit cell is composed of: two antibody chambers divided by a reaction chamber (1–2), 4 MITOMI buttons (3), a valve that segregates the unit cells (4), a valve that separates antibody and reaction chambers (5) and a valve for releasing pressure in the antibody chambers (6). b) The PDMS chip is aligned to an epoxy-functionalized slide onto which primary and secondary antibodies were spotted. c) Assay details: schematic of the unit cell and cross section of a button region: i) functionalization of the surface: BSA-biotin is flowed though the chip followed by neutravidin. Next, the buttons are closed and BSA-biotin flowed again to passivate all neutravidin molecules except for those located underneath the MITOMI buttons, ii) the biotinylated primary antibody is allowed to diffuse into the MITOMI detection chamber and is bound by neutravidin immobilizing it in the MITOMI detection regions, iii) the sample is flown through the device and antigens are captured by the surface immobilized antibodies, iv) finally, the fluorescently labeled secondary antibody is allowed to diffuse into the MITOMI area, binds to the antigen if present, and is trapped by MITOMI. The entire device is then quantitated using a DNA microarray scanner.

Article Snippet: The microfluidic device was scanned using a fluorescent microarray scanner (ArrayWorx e-Biochip Reader, Applied Precision, USA).

Techniques: Control, Labeling, Microarray