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wcxii protein chip arrays  (Ciphergen inc)

 
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    Ciphergen inc wcxii protein chip arrays
    Wcxii Protein Chip Arrays, 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/protein+chip+array/wcxii+protein+chip+arrays/us07781180-197-12-16
    Average 90 stars, based on 1 article reviews
    wcxii protein chip arrays - by Bioz Stars, 2026-11
    90/100 stars

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    other:

    Article Title: Molecular stages of rapid and uniform neuralization of human embryonic stem cells
    Article Snippet: RT/Q-PCR Undifferentiated ESC clusters growing in SM for 6 days and NPCs grown for an additional 5-6 days in EM were collected and lysed in Trizol (Sigma) for RNA isolation.

    Article Title: Screening for potential serum biomarkers in rat mesangial proliferative nephritis.
    Article Snippet: Received: October 22, 2015 Revised: December 28, 2015 Accepted: January 18, 2016 Mesangial proliferative nephritis (MesPGN) is a common kidney disease worldwide.. The main feature of the disease is mesangial cell proliferation-induced injury to kidney function.. In this study, we explored serum biomarkers for kidney function injury in anti-Thy1 nephritis.

    Article Title: Effects of pretreatment protocols on human amniotic fluid protein profiling with SELDI-TOF MS using protein chips and magnetic beads.
    Article Snippet: a Institute of Basic Medical Sciences, Qilu Hospital, Shandong University, 107 Wenhua Xi Road, Jinan, 250012, Shandong, PR China b Department of Clinical Laboratory, Qilu Hospital, Shandong University, 107 Wenhua Xi Road, Jinan 250012, Shandong, PR China c Key Laboratory of Cardiovascular Proteomics of Shandong Province, Qilu Hospital, Shandong University, 107 Wenhua Xi Road, Jinan, 250012, Shandong, PR China

    Marker:

    Article Title: Marker proteins for diagnosing liver disease and method of diagnosing liver disease using the same
    Article Snippet: .. Identification of marker proteins for diagnosing liver disease by the use of WCXII protein chip arrays Next, using exactly the same samples as in Example 1, novel markers for liver trouble in the sera were searched for by the use of WCXII protein chip arrays (Ciphergen Biosystems, Inc.). ..



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    Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization <t>time-of-flight</t> <t>(SELDI-TOF)</t> mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.
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    Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization time-of-flight (SELDI-TOF) mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.

    Journal: Breast Cancer Research : BCR

    Article Title: Novel serum protein biomarker panel revealed by mass spectrometry and its prognostic value in breast cancer

    doi: 10.1186/bcr3676

    Figure Lengend Snippet: Identification of serum proteins by immunodepletion and western blotting. Proteins representing peaks at m/z 6624, m/z 8916 and m/z 13870 were immunodepleted from serum extracts using monoclonal antibodies against (A) apolipoprotein CI (ApoCI), (B) C3a/ C3a des-arginine anaphylatoxin (C3a-desArg) or (C) transthyretin. The starting material (Starting, upper panel), the immunodepleted sample (Depleted, middle panel) and the eluted fraction (Recovered, lower panel) were analyzed on NP20 arrays by surface-enhanced laser desorption/ionization time-of-flight (SELDI-TOF) mass spectrometry (MS). (D) Western blotting for ApoCI, C3a/C3a-desArg and transthyretin were performed on four healthy volunteer (HV) samples and four breast cancer patient (BC) samples. (E) Mean band densities (+standard deviation (SD)) derived from the blots shown in panel D (n = 4 for all groups). (F-H) Association between SELDI peak intensities and western blotting band densities for individual HV and BC serum samples (n = 8), indicating strong correlations for (F) ApoCI, (G) C3a-desArg and (H) transthyretin.

    Article Snippet: All serum samples were initially denatured in buffer containing 8 M urea, 1% CHAPS (3-[(3-cholamidopropyl) dimethylammonio]-1-propanesulfate) and analyzed by TOF MS on SELDI protein chip arrays (Bio-Rad, Hercules, CA, USA) as previously described [ ].

    Techniques: Western Blot, Mass Spectrometry, Standard Deviation, Derivative Assay