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Arrayjet Limited non-contact microarray robot
Non Contact Microarray Robot, supplied by Arrayjet Limited, 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+robot/microarray+robot+sprint/pm40623969-391-30-33
Average 90 stars, based on 1 article reviews
non-contact microarray robot - by Bioz Stars, 2026-09
90/100 stars

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Related Articles

Membrane:

Article Title: A New Versatile Microarray-based Method for High Throughput Screening of Carbohydrate-active Enzymes
Article Snippet: The filled plates were incubated (Ecotron, INFORS HT, Switzerland) at 100 rpm for a specific time and temperature (specified in the figure legends) followed by 10 min at 80 °C. .. After spinning down the plates for 10 min at 4000 rpm, the plate content was printed at 22 °C and 55% humidity onto nitrocellulose membrane with a pore size of 0.45 μm (Whatman) using a microarray robot (Sprint, Arrayjet, Roslin, UK). ..

Article Title: Cell wall composition profiling of parasitic giant dodder (Cuscuta reflexa) and its hosts: a priori differences and induced changes.
Article Snippet: The microtiter plate was covered with adhesive film to avoid evaporation and incubated for 2 h at 30°C 2015 The Authors New Phytologist 2015 New Phytologist Trust New Phytologist (2015) 207: 805–816 www.newphytologist.com New Phytologist Research 807 and 100 rpm agitation (Ecotron, INFORS HT, Bottmingen, Switzerland), followed by a heat inactivation for 10 min at 80°C. .. The content of the plate was spotted as microarrays onto sheets of nitrocellulose membrane with a pore size of 0.45 lm (Whatman) by using a microarray robot (Sprint, Arrayjet). ..

Pore Size:

Article Title: A New Versatile Microarray-based Method for High Throughput Screening of Carbohydrate-active Enzymes
Article Snippet: The filled plates were incubated (Ecotron, INFORS HT, Switzerland) at 100 rpm for a specific time and temperature (specified in the figure legends) followed by 10 min at 80 °C. .. After spinning down the plates for 10 min at 4000 rpm, the plate content was printed at 22 °C and 55% humidity onto nitrocellulose membrane with a pore size of 0.45 μm (Whatman) using a microarray robot (Sprint, Arrayjet, Roslin, UK). ..

Article Title: Cell wall composition profiling of parasitic giant dodder (Cuscuta reflexa) and its hosts: a priori differences and induced changes.
Article Snippet: The microtiter plate was covered with adhesive film to avoid evaporation and incubated for 2 h at 30°C 2015 The Authors New Phytologist 2015 New Phytologist Trust New Phytologist (2015) 207: 805–816 www.newphytologist.com New Phytologist Research 807 and 100 rpm agitation (Ecotron, INFORS HT, Bottmingen, Switzerland), followed by a heat inactivation for 10 min at 80°C. .. The content of the plate was spotted as microarrays onto sheets of nitrocellulose membrane with a pore size of 0.45 lm (Whatman) by using a microarray robot (Sprint, Arrayjet). ..

Microarray:

Article Title: A New Versatile Microarray-based Method for High Throughput Screening of Carbohydrate-active Enzymes
Article Snippet: The filled plates were incubated (Ecotron, INFORS HT, Switzerland) at 100 rpm for a specific time and temperature (specified in the figure legends) followed by 10 min at 80 °C. .. After spinning down the plates for 10 min at 4000 rpm, the plate content was printed at 22 °C and 55% humidity onto nitrocellulose membrane with a pore size of 0.45 μm (Whatman) using a microarray robot (Sprint, Arrayjet, Roslin, UK). ..

Article Title: Characterisation of a novel endo-xyloglucanase (XcXGHA) from Xanthomonas that accommodates a xylosyl-substituted glucose at subsite -1.
Article Snippet: A xyloglucan-specific endo-1,4β-glucanase (XcXGHA) from Xanthomonas citri pv. mangiferaeindicae has been cloned, expressed in Escherichia coli, purified and characterised.. The XcXGHA enzyme belongs to CAZy family GH74 and has catalytic site residues conserved with other xyloglucanases in this family.. At its optimal reaction conditions, pH 7.0 and 40 °C, the enzyme has a kcat/KM value of 2.2×10 min M on a tamarind seed xyloglucan substrate.

Article Title: Cell wall composition profiling of parasitic giant dodder (Cuscuta reflexa) and its hosts: a priori differences and induced changes.
Article Snippet: The microtiter plate was covered with adhesive film to avoid evaporation and incubated for 2 h at 30°C 2015 The Authors New Phytologist 2015 New Phytologist Trust New Phytologist (2015) 207: 805–816 www.newphytologist.com New Phytologist Research 807 and 100 rpm agitation (Ecotron, INFORS HT, Bottmingen, Switzerland), followed by a heat inactivation for 10 min at 80°C. .. The content of the plate was spotted as microarrays onto sheets of nitrocellulose membrane with a pore size of 0.45 lm (Whatman) by using a microarray robot (Sprint, Arrayjet). ..

Article Title: Novel α-L-Fucosidases from a Soil Metagenome for Production of Fucosylated Human Milk Oligosaccharides
Article Snippet: .. 4 M NaOH (containing 0.1 % NaBH4) extracts from the different plant species were spotted using a microarray robot (Sprint, Arrayjet, Roslin, UK). ..



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Figure 2. (A) Layout of the biomarker <t>microarray</t> (BMA) slide, showing the arrangement of capture antibodies and controls within each well. (B) Illustration of the BMA slide design with 16 wells and its alignment within the slide holder for analysis. The numbers along the side correspond to the row numbers of each well, while the numbers along the bottom represent the column positions of the slide.
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Image Search Results


Figure 2. (A) Layout of the biomarker microarray (BMA) slide, showing the arrangement of capture antibodies and controls within each well. (B) Illustration of the BMA slide design with 16 wells and its alignment within the slide holder for analysis. The numbers along the side correspond to the row numbers of each well, while the numbers along the bottom represent the column positions of the slide.

Journal: Micromachines

Article Title: Portable Fluorescence Microarray Reader-Enabled Biomarker Panel Detection System for Point-of-Care Diagnosis of Lupus Nephritis.

doi: 10.3390/mi16020156

Figure Lengend Snippet: Figure 2. (A) Layout of the biomarker microarray (BMA) slide, showing the arrangement of capture antibodies and controls within each well. (B) Illustration of the BMA slide design with 16 wells and its alignment within the slide holder for analysis. The numbers along the side correspond to the row numbers of each well, while the numbers along the bottom represent the column positions of the slide.

Article Snippet: The slides were prepared using a non-contact microarray printing robot (sciFLEXARRAYER S3; Scienion GmbH, Berlin, Germany), which printed capture antibodies for each biomarker in triplicate at a controlled drop volume of 450 ± 20 pL.

Techniques: Biomarker Discovery, Microarray