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seldi proteinchip arrays weak cation exchange (wcx-2  (Ciphergen inc)

 
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    Structured Review

    Ciphergen inc seldi proteinchip arrays weak cation exchange (wcx-2
    Seldi Proteinchip Arrays Weak Cation Exchange (Wcx 2, 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/weak+cation+exchanger+array/seldi+proteinchip/pmc03312904-100-6-10
    Average 90 stars, based on 1 article reviews
    seldi proteinchip arrays weak cation exchange (wcx-2 - by Bioz Stars, 2026-11
    90/100 stars

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    Related Articles

    other:

    Article Title: A Classification Method Based on Principal Components of SELDI Spectra to Diagnose of Lung Adenocarcinoma
    Article Snippet: The SELDI ProteinChip arrays of weak cation exchange (WCX-2) from Ciphergen Biosystems were used for protein capture.

    Article Title: Effect of green tea on blood glucose levels and serum proteomic patterns in diabetic (db/db) mice and on glucose metabolism in healthy humans
    Article Snippet: The spots were analyzed using the SELDI ProteinChip system (PBS-IIc, Ciphergen Biosystems).

    Article Title: Predicting Early Intrahepatic Recurrence of Hepatocellular Carcinoma after Microwave Ablation Using SELDI-TOF Proteomic Signature
    Article Snippet: Serum samples were analyzed with the SELDI ProteinChip system (Ciphergen Biosystems) to obtain a quantitative proteomic profile.

    Article Title: Transcription chip
    Article Snippet: At present, a protein chip system using SELDI-TOF MS from Ciphergen is commercially available, and the protein chip to which the antibody has been immobilized using this system has been developed, but it is not sufficient in terms of throughput property and accuracy of mass analysis.

    Article Title: Cross-platform Analysis of Cancer Biomarkers: A Bayesian Network Approach to Incorporating Mass Spectrometry and Microarray Data
    Article Snippet: It was collected using an H4 protein chip and a Ciphergen PBS1 SELDI-TOF (Surface-Enhanced Laser Desorption and Ionization Time of Flight) mass spectrometer.

    Biomarker Discovery:

    Article Title: Data analysis method and system
    Article Snippet: .. Further, in the manuscript by Mian and colleagues (Mian, et al., 2005) predictive performance was based primarily on spectra obtained from Ciphergen SELDI chip platform which are associated with inherent low-resolution read-outs using low-resolution MS equipment whereas here protein biomarker detection was carried out using a higher resolution MALDI-MS analyzer, so the m/z value of 11700 may have some variation associated with it. ..

    Binding Assay:

    Article Title: Compositions for binding to assay substrata and methods of using
    Article Snippet: .. Doubly-coated microparticle dispersions loaded with the fluorescent dye Rhodamine B base were prepared using the same procedure as in Example 1, then tested for binding to Ciphergen SELDI chips. ..

    Mass Spectrometry:

    Article Title: Biomarkers for amyotrophic lateral sclerosis
    Article Snippet: .. Mass Spectroscopy Mass spectroscopy was performed using SELDI ProteinChip® technology (Ciphergen Biosystems, Inc., Fremont, Calif.). ..



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    L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on <t>CM10</t> array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).
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    Image Search Results


    L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on CM10 array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).

    Journal: Proteome Science

    Article Title: S100A10 protein expression is associated with oxaliplatin sensitivity in human colorectal cancer cells

    doi: 10.1186/1477-5956-9-76

    Figure Lengend Snippet: L-OHP sensitivity and candidate peak selection . (A) Protein expression profiles of each cell line on CM10 array at pH 4.5. The candidate peak is enclosed by the rectangle. (B) Peak intensity of the 11.1 kDa protein in 11 CRC cell lines strongly correlates with L-OHP sensitivity. The peak intensity and IC 50 value of each cell line are plotted as means ± S.D. (peak intensity, n = 3; IC 50 , n = 3 or 4).

    Article Snippet: Weak cation-exchange ProteinChip CM10 arrays (Bio-Rad Laboratories, Hercules, CA, USA) were used for protein profiling.

    Techniques: Selection, Expressing

    Characterization of the 11.1 kDa protein . (A) Estimation of pI of the 11.1 kDa protein. The affinity of the 11.1 kDa protein (indicated by the arrow) to a CM10 array changed with a pH range of 3.0-10.0. (B) Estimation of experimental molecular mass of the 11.1 kDa protein (indicated by the arrow). Bovine insulin (5733.5 Da) and equine cytochrome C (12361.0 Da) were calibrants for internal calibration.

    Journal: Proteome Science

    Article Title: S100A10 protein expression is associated with oxaliplatin sensitivity in human colorectal cancer cells

    doi: 10.1186/1477-5956-9-76

    Figure Lengend Snippet: Characterization of the 11.1 kDa protein . (A) Estimation of pI of the 11.1 kDa protein. The affinity of the 11.1 kDa protein (indicated by the arrow) to a CM10 array changed with a pH range of 3.0-10.0. (B) Estimation of experimental molecular mass of the 11.1 kDa protein (indicated by the arrow). Bovine insulin (5733.5 Da) and equine cytochrome C (12361.0 Da) were calibrants for internal calibration.

    Article Snippet: Weak cation-exchange ProteinChip CM10 arrays (Bio-Rad Laboratories, Hercules, CA, USA) were used for protein profiling.

    Techniques: