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microsys 5100-4sq non-contact robotic microarray spotting system  (Digilab Inc)

 
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    Digilab Inc microsys 5100-4sq non-contact robotic microarray spotting system
    Microsys 5100 4sq Non Contact Robotic Microarray Spotting System, supplied by Digilab 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/product/microarray-spotting+robot/microsys++5100+4sq+microarray+spotter/pmc05106528-168-2-4
    Average 90 stars, based on 1 article reviews
    microsys 5100-4sq non-contact robotic microarray spotting system - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    other:

    Article Title: Microarray platform affords improved product analysis in mammalian cell growth studies
    Article Snippet: The PLL-Ba 2+ mixture was spotted onto poly(styrene-co-maleic anhydride) (PSMA) coated glass slides using a MicrosSys 5100-4SQ microcontact microarray spotter (DigiLab), making a 6 × 8 × 8 patterned array of 60 nl spots on the chip and allowing them to dry.

    Article Title: High-Throughput Discovery of Targeted, Minimally Complex Peptide Surfaces for Human Pluripotent Stem Cell Culture.
    Article Snippet: Human pluripotent stem cells harbor an unlimited capacity to generate therapeutically relevant cells for applications in regenerative medicine.. However, to utilize these cells in the clinic, scalable culture systems that activate defined receptors and signaling pathways to sustain stem cell self-renewal are required; and synthetic materials offer considerable promise to meet these needs.. De novo development of materials that target novel pathways has been stymied by a limited understanding of critical receptor interactions maintaining pluripotency.

    Article Title: Fibroblast Growth Factor-based Signaling through Synthetic Heparan Sulfate Blocks Copolymers Studied Using High Cell Density Three-dimensional Cell Printing
    Article Snippet: A freshly prepared solution of 0.1 m m BaCl 2 and poly- l -lysine solution (0.1% w/v) was mixed (1:2) and microarrayed (spotted) onto the slide in a 2 × 4-block pattern, with a 6 × 8 spot array in each block, using MicrosSys 5100–4SQ microcontact microarray spotter (Digilab, Inc., Marlborough, MA).

    Article Title: High-Throughput Toxicity and Phenotypic Screening of 3D Human Neural Progenitor Cell Cultures on a Microarray Chip Platform
    Article Snippet: An enclosed MicroSys 5100-4SQ (DigiLab) non-contact robotic microarray spotting system was used for printing.

    Article Title: Fibroblast Growth Factor-based Signaling through Synthetic Heparan Sulfate Blocks Copolymers Studied Using High Cell Density Three-dimensional Cell Printing
    Article Snippet: A freshly prepared solution of 0.1 mM BaCl2 and poly-L-lysine solution (0.1% w/v) was mixed (1:2) and microarrayed (spotted) onto the slide in a 2 4-block pattern, with a 6 8 spot array in each block, using MicrosSys 5100 – 4SQ microcontact microarray spotter (Digilab, Inc., Marlborough, MA).

    Article Title: Fibroblast Growth Factor-based Signaling through Synthetic Heparan Sulfate Blocks Copolymers Studied Using High Cell Density Three-dimensional Cell Printing
    Article Snippet: The poly(styrene co-malic anhydride) solution was then spin-coated onto acid-washed microscope slides using a Laurell Technologies (North Wales, PA) WS-400B spin-coater.

    Article Title: Metabolic Enzyme Microarray Coupled with Miniaturized Cell-Culture Array Technology for High-Throughput Toxicity Screening
    Article Snippet: Immediately before spotting the sol solution onto the slides, mix 3 mL of the MTMOS–HCl sol solution with 1 mL of Dulbecco’s PBS without CaCl 2 and MgCl 2 and use this mixture within 1 h. After aligning the MTMOS-coated slides on the slide deck of a MicroSysTM 5100-4SQ microarray spotter (Genomics Solutions, now Digilab, Inc.), print the mixture onto the periphery of each slide (typically 80 spots/slide, 450 nL per spot, 2 mm spot-to-spot distance).

    Microarray:

    Article Title: FGF-FGFR Signaling Mediated through Glycosaminoglycans in Microtiter Plate and Cell-Based Microarray Platforms
    Article Snippet: .. A 30 nL solution of a 0.1 mM BaCl 2 :poly-L-lysine (1:2) was spotted onto PSMA coated slides using a MicroSys 5100-4SQ non contact microarray spotter (Genomic Solutions, now Digilab, Inc., Marlborough, MA) and left to dry for approximately 1 h. Briefly, this microarray-based approach employs pump-based aspiration and dispensing through a 100 micron ceramic tip with high positional accuracy. ..



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    Identification of the RLR sequence as a potential MIF binding region to the N-terminal peptide of CXCR4. ( a , b ) The peptide spot microarray method suggests that the RLR tripeptide at sequence position 87–89 may contribute to MIF/CXCR4 binding. A peptide spot array containing 15-mer spotted MIF peptides positionally shifted by three amino acids were probed with biotin-CXCR4(1–27). Graphs are plots of spotted MIF peptides over the intensity of the binding signal to biotin-CXCR4(1–27) as read-out by streptavidin Cy5.5 fluorescence. ( a ) Of five positionally shifted 15-mer peptides of the region 79–105 only peptides containing RLR interact with CXCR4(1–27). ( b ) Binding of RLR-containing MIF peptides is modulated by N-terminal extension, but residues N-terminal of RLR do not exhibit binding activity per se . ( c ) Structural model of MIF (as monomer and trimer) and position of the N-like loop (green) and the RLR sequence (red). Note: in the three-dimensional conformation of the monomer, RLR is located in the vicinity of the N-like loop of MIF. The trimeric structure shows that both the N-like loop and RLR are surface-exposed on the trimer (see also Fig. ).

    Journal: Scientific Reports

    Article Title: Identification of an Arg-Leu-Arg tripeptide that contributes to the binding interface between the cytokine MIF and the chemokine receptor CXCR4

    doi: 10.1038/s41598-018-23554-5

    Figure Lengend Snippet: Identification of the RLR sequence as a potential MIF binding region to the N-terminal peptide of CXCR4. ( a , b ) The peptide spot microarray method suggests that the RLR tripeptide at sequence position 87–89 may contribute to MIF/CXCR4 binding. A peptide spot array containing 15-mer spotted MIF peptides positionally shifted by three amino acids were probed with biotin-CXCR4(1–27). Graphs are plots of spotted MIF peptides over the intensity of the binding signal to biotin-CXCR4(1–27) as read-out by streptavidin Cy5.5 fluorescence. ( a ) Of five positionally shifted 15-mer peptides of the region 79–105 only peptides containing RLR interact with CXCR4(1–27). ( b ) Binding of RLR-containing MIF peptides is modulated by N-terminal extension, but residues N-terminal of RLR do not exhibit binding activity per se . ( c ) Structural model of MIF (as monomer and trimer) and position of the N-like loop (green) and the RLR sequence (red). Note: in the three-dimensional conformation of the monomer, RLR is located in the vicinity of the N-like loop of MIF. The trimeric structure shows that both the N-like loop and RLR are surface-exposed on the trimer (see also Fig. ).

    Article Snippet: Analysis of interactions was performed using a microarray processing station (Intavis Slide Spotting Robot).

    Techniques: Sequencing, Binding Assay, Microarray, Fluorescence, Activity Assay