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Ciphergen inc q10 chip
Q10 Chip, supplied by Ciphergen 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/q10+chip/q10+chip/us08437964-557-32-34
Average 90 stars, based on 1 article reviews
q10 chip - by Bioz Stars, 2026-10
90/100 stars

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Related Articles

Fractionation:

Article Title: Apolipoprotein AII levels are associated with the UP/UCr levels in idiopathic steroid-sensitive nephrotic syndrome.
Article Snippet: Background Various humoral factors have been proposed as causal agents of idiopathic steroid-sensitive nephrotic syndrome (ISSNS), resulting in varying data.. We used mass spectrometry (MS) to analyze serum proteins in a search for proteins that might be involved in ISSNS pathophysiology.. Methods Serial serum samples were obtained from 33 children with ISSNS.

Purification:

Article Title: Apolipoprotein AII levels are associated with the UP/UCr levels in idiopathic steroid-sensitive nephrotic syndrome.
Article Snippet: Background Various humoral factors have been proposed as causal agents of idiopathic steroid-sensitive nephrotic syndrome (ISSNS), resulting in varying data.. We used mass spectrometry (MS) to analyze serum proteins in a search for proteins that might be involved in ISSNS pathophysiology.. Methods Serial serum samples were obtained from 33 children with ISSNS.

Clinical Proteomics:

Article Title: Systems and methods involving data patterns such as spectral biomarkers
Article Snippet: .. The aliquots were sent for mass spectra analysis at the Clinical Proteomics Reference Laboratory using Surface Enhanced Laser Desorption Ionization mass spectrometer (Ciphergen, Fremont, Calif.) according to the following protocol: (1) a Q10 chip (Ciphergen) was twice treated with phosphate buffer for 5 minutes; (2) each aliquot was added to each well of the chip and incubated for 60 minutes at room temperature; (3) the chip was washed three times with 150 microliters of phosphate buffer using 10 mixing cycles, followed by a single wash with water; (4) The chip was air dried for 10 minutes; (5) 1 microliter of SPA matrix in 50% acetonitrile/water with 0.5% TFA was added to the chip, which was then air dried for 15 minutes; (6) step (5) was repeated. ..

Mass Spectrometry:

Article Title: Systems and methods involving data patterns such as spectral biomarkers
Article Snippet: .. The aliquots were sent for mass spectra analysis at the Clinical Proteomics Reference Laboratory using Surface Enhanced Laser Desorption Ionization mass spectrometer (Ciphergen, Fremont, Calif.) according to the following protocol: (1) a Q10 chip (Ciphergen) was twice treated with phosphate buffer for 5 minutes; (2) each aliquot was added to each well of the chip and incubated for 60 minutes at room temperature; (3) the chip was washed three times with 150 microliters of phosphate buffer using 10 mixing cycles, followed by a single wash with water; (4) The chip was air dried for 10 minutes; (5) 1 microliter of SPA matrix in 50% acetonitrile/water with 0.5% TFA was added to the chip, which was then air dried for 15 minutes; (6) step (5) was repeated. ..

Incubation:

Article Title: Systems and methods involving data patterns such as spectral biomarkers
Article Snippet: .. The aliquots were sent for mass spectra analysis at the Clinical Proteomics Reference Laboratory using Surface Enhanced Laser Desorption Ionization mass spectrometer (Ciphergen, Fremont, Calif.) according to the following protocol: (1) a Q10 chip (Ciphergen) was twice treated with phosphate buffer for 5 minutes; (2) each aliquot was added to each well of the chip and incubated for 60 minutes at room temperature; (3) the chip was washed three times with 150 microliters of phosphate buffer using 10 mixing cycles, followed by a single wash with water; (4) The chip was air dried for 10 minutes; (5) 1 microliter of SPA matrix in 50% acetonitrile/water with 0.5% TFA was added to the chip, which was then air dried for 15 minutes; (6) step (5) was repeated. ..



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Image Search Results


Identification and validation of peak 3790 as prothymosin- α . Mass spectrum of proteins from fraction Q3 that bound to Q10 ProteinChip array and was analyzed on QSTAR XL instrument (mass range from 1000 to 4000 m/z).

Journal: Journal of Biomedicine and Biotechnology

Article Title: Proteomic Analysis of Pichindé virus Infection Identifies Differential Expression of Prothymosin- α

doi: 10.1155/2010/956823

Figure Lengend Snippet: Identification and validation of peak 3790 as prothymosin- α . Mass spectrum of proteins from fraction Q3 that bound to Q10 ProteinChip array and was analyzed on QSTAR XL instrument (mass range from 1000 to 4000 m/z).

Article Snippet: The mass spectra of the proteins captured on Q10 chips were recorded on the PCS 4000 ProteinChip array reader (Bio-Rad laboratories, Hercules, CA).

Techniques: