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full moon biosystems scanning array service  (Full Moon BioSystems)

 
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    Full Moon BioSystems full moon biosystems scanning array service
    Full Moon Biosystems Scanning Array Service, supplied by Full Moon BioSystems, 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/antibody+microarray+service/array+scanning+and+data+analysis/pmc04015682-214-18-15
    Average 90 stars, based on 1 article reviews
    full moon biosystems scanning array service - by Bioz Stars, 2026-10
    90/100 stars

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    Related Articles

    Microarray:

    Article Title: HIV-1 induces cytoskeletal alterations and Rac1 activation during monocyte-blood–brain barrier interactions: modulatory role of CCR5
    Article Snippet: .. The antibody microarray was performed according to the manufacturer’s protocol and slides were scanned using Full Moon Biosystems Scanning Array Service. ..

    Phospho-proteomics:

    Article Title: Differentiation of Essential Oils Using Nanofluidic Protein Post-Translational Modification Profiling
    Article Snippet: Antibody arrays were acquired from Full Moon Biosystems (Cat. No. PMT138, Sunnyvale, CA) and performed according to manufacturer’s protocol. .. Array scanning and data analysis were performed by Full Moon Biosystem. (d-e) Detection of (d) increased STAT1 phosphorylation and (e) increased STAT6 phosphorylation with nanofluidic protein PTM profiling following the treatment of HepG2 cells with copaiba essential oil. ..



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    Image Search Results


    Downstream signaling hits between cells expressing wild-type PBK and cells expressing p.Gly43Arg PBK (control and treatment) for 24 hours as analyzed by KAM-900P Antibody Microarray.

    Journal: Scientific Reports

    Article Title: A novel loss-of-function mutation of PBK associated with human kidney stone disease

    doi: 10.1038/s41598-020-66936-4

    Figure Lengend Snippet: Downstream signaling hits between cells expressing wild-type PBK and cells expressing p.Gly43Arg PBK (control and treatment) for 24 hours as analyzed by KAM-900P Antibody Microarray.

    Article Snippet: Protein phosphorylation in HEK293T cells transfected with plasmid construct containing either WT-PBK cDNA or mutant-p.G43R-PBK cDNA was examined by KAM-900P Antibody Microarray Service (Kinexus Bioinformatics Corporation, Vancouver, Canada).

    Techniques: Expressing, Control, Microarray

    Kinexus antibody microarray. Fibroblast growth factor receptor-like protein 1 (FGFRL1) inducible cells (clone K3F) were cultivated for 32 h in the presence or absence of the inducer doxycycline. Protein extracts were prepared and analyzed on Kinexus antibody microarrays containing more than 650 different antibodies against various signaling proteins. No significant differences were observed between doxycycline-treated and untreated cells (not shown). To verify some of the results, the two protein extracts were separated on SDS polyacrylamide gels, transferred to an immunoblot membrane and probed with antibodies against 18 selected proteins as indicated using a multiscreen apparatus from BioRad. The immunoblot was analyzed with a chemiluminescence imager. No significant differences were observed between doxycycline-induced (lower panel) and uninduced (top panel) cells. The migration positions of molecular weight markers are shown in the left and right margins by short horizontal lines. These lines correspond (from top to bottom) to 250 K, 150 K, 100 K, 75 K, 50 K, 37 K, 25 K, 20 K and 15 K.

    Journal: International Journal of Molecular Medicine

    Article Title: Receptor FGFRL1 does not promote cell proliferation but induces cell adhesion

    doi: 10.3892/ijmm.2016.2601

    Figure Lengend Snippet: Kinexus antibody microarray. Fibroblast growth factor receptor-like protein 1 (FGFRL1) inducible cells (clone K3F) were cultivated for 32 h in the presence or absence of the inducer doxycycline. Protein extracts were prepared and analyzed on Kinexus antibody microarrays containing more than 650 different antibodies against various signaling proteins. No significant differences were observed between doxycycline-treated and untreated cells (not shown). To verify some of the results, the two protein extracts were separated on SDS polyacrylamide gels, transferred to an immunoblot membrane and probed with antibodies against 18 selected proteins as indicated using a multiscreen apparatus from BioRad. The immunoblot was analyzed with a chemiluminescence imager. No significant differences were observed between doxycycline-induced (lower panel) and uninduced (top panel) cells. The migration positions of molecular weight markers are shown in the left and right margins by short horizontal lines. These lines correspond (from top to bottom) to 250 K, 150 K, 100 K, 75 K, 50 K, 37 K, 25 K, 20 K and 15 K.

    Article Snippet: The extracts were analyzed by the Kinexus antibody microarray service, which utilizes >650 verified antibodies against most well-studied signaling proteins, including phospholipase Cγ, PI3-kinase, STAT and Akt.

    Techniques: Microarray, Western Blot, Migration, Molecular Weight