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cation exchange proteinchip array  (Bio-Rad)


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    Bio-Rad cation exchange proteinchip array
    Cation Exchange Proteinchip Array, supplied by Bio-Rad, used in various techniques. Bioz Stars score: 93/100, based on 86 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/cation+exchange+array+cm10/ProteinChip+CM10+Arrays/us09459254-176-12-16
    Average 93 stars, based on 86 article reviews
    cation exchange proteinchip array - by Bioz Stars, 2026-10
    93/100 stars

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    Related Articles

    Chromatin Immunoprecipitation:

    Article Title: Gross Cystic Disease Fluid Protein-15(GCDFP-15)/Prolactin-Inducible Protein (PIP) as Functional Salivary Biomarker for Primary Sjögren’s Syndrome
    Article Snippet: .. The ProteinChip System, Series 4000 Personal Edition (Ciphergen Biosystems, Inc) was used to perform SELDI-TOF MS. After preliminary experiments with different protein chip arrays (including Q10, IMAC30 and H50, Bio-Rad), the cation exchange array CM10 (Bio-Rad) - a weak cation exchange chip - was selected to give the best results and prepared according to the manufacturer’s instructions. ..



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    Protein profiling analysis of TC and FB supernatants by surface-enhanced laser desorption and ionization mass spectrometry. Characteristic proteins that are secreted by TCs were identified at m/z values of ∼11.7 kD, from 13.8 to 14.8, and at 22.5 kD. The peaks suggest the presence of MIP-1α, MIP-2 dimer, MCP-1 and VEGF. m/z range: 0–25,000 D, <t>CM10</t> chips, SPA matrix. Control – cell culture medium, TC-P1 – first passage, TC-P2 – second passage, TC-P3 – third passage, FB – fibroblasts.
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    Protein profiling analysis of TC and FB supernatants by surface-enhanced laser desorption and ionization mass spectrometry. Characteristic proteins that are secreted by TCs were identified at m/z values of ∼11.7 kD, from 13.8 to 14.8, and at 22.5 kD. The peaks suggest the presence of MIP-1α, MIP-2 dimer, MCP-1 and VEGF. m/z range: 0–25,000 D, <t>CM10</t> chips, SPA matrix. Control – cell culture medium, TC-P1 – first passage, TC-P2 – second passage, TC-P3 – third passage, FB – fibroblasts.
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    Protein profiling analysis of TC and FB supernatants by surface-enhanced laser desorption and ionization mass spectrometry. Characteristic proteins that are secreted by TCs were identified at m/z values of ∼11.7 kD, from 13.8 to 14.8, and at 22.5 kD. The peaks suggest the presence of MIP-1α, MIP-2 dimer, MCP-1 and VEGF. m/z range: 0–25,000 D, CM10 chips, SPA matrix. Control – cell culture medium, TC-P1 – first passage, TC-P2 – second passage, TC-P3 – third passage, FB – fibroblasts.

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: The secretome of myocardial telocytes modulates the activity of cardiac stem cells

    doi: 10.1111/jcmm.12624

    Figure Lengend Snippet: Protein profiling analysis of TC and FB supernatants by surface-enhanced laser desorption and ionization mass spectrometry. Characteristic proteins that are secreted by TCs were identified at m/z values of ∼11.7 kD, from 13.8 to 14.8, and at 22.5 kD. The peaks suggest the presence of MIP-1α, MIP-2 dimer, MCP-1 and VEGF. m/z range: 0–25,000 D, CM10 chips, SPA matrix. Control – cell culture medium, TC-P1 – first passage, TC-P2 – second passage, TC-P3 – third passage, FB – fibroblasts.

    Article Snippet: The cell culture supernatants from mouse TCs and BALBc/3T3 cells were analysed in triplicate on a weak cation-exchange (CM10) ProteinChip array (Bio-Rad Laboratories, Hercules, CA, USA).

    Techniques: Mass Spectrometry, Control, Cell Culture

    (A) Proteins that were secreted in the cell culture supernatants of rat myocardial TCs as assessed by SELDI-TOF-MS analysis. A significant enhancement of the 14.8 kD peak in TC mono-culture compared with CSC mono-culture and TC-CSC co-culture is evident. m/z range: 10,000–20,000 D, CM10 chips, SPA matrix. (B) Outline of the 22.2 kD peak (IL-6) in the SELDI-TOF-MS spectra of proteins that were secreted by rat TCs. CM10 chips, SPA matrix. The expression of the protein associated with this peak does not significantly differ between the TC and TC-CSC co-cultures.

    Journal: Journal of Cellular and Molecular Medicine

    Article Title: The secretome of myocardial telocytes modulates the activity of cardiac stem cells

    doi: 10.1111/jcmm.12624

    Figure Lengend Snippet: (A) Proteins that were secreted in the cell culture supernatants of rat myocardial TCs as assessed by SELDI-TOF-MS analysis. A significant enhancement of the 14.8 kD peak in TC mono-culture compared with CSC mono-culture and TC-CSC co-culture is evident. m/z range: 10,000–20,000 D, CM10 chips, SPA matrix. (B) Outline of the 22.2 kD peak (IL-6) in the SELDI-TOF-MS spectra of proteins that were secreted by rat TCs. CM10 chips, SPA matrix. The expression of the protein associated with this peak does not significantly differ between the TC and TC-CSC co-cultures.

    Article Snippet: The cell culture supernatants from mouse TCs and BALBc/3T3 cells were analysed in triplicate on a weak cation-exchange (CM10) ProteinChip array (Bio-Rad Laboratories, Hercules, CA, USA).

    Techniques: Cell Culture, Co-Culture Assay, Expressing