mauricetm compasstm software (Protein Simple Inc)
Protein Simple Inc is a verified supplier 
Protein Simple Inc manufactures this product 
96
Structured Review
Protein Simple Inc
mauricetm compasstm software
Mauricetm Compasstm Software, supplied by Protein Simple Inc, used in various techniques. Bioz Stars score: 96/100, based on 141 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/compasstm+software/Maurice/us12304955-771-32-35
Average 96 stars, based on 141 article reviews
Mauricetm Compasstm Software, supplied by Protein Simple Inc, used in various techniques. Bioz Stars score: 96/100, based on 141 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
https://www.bioz.com/product/compasstm+software/Maurice/us12304955-771-32-35
Average 96 stars, based on 141 article reviews
mauricetm compasstm software - by Bioz Stars,
2026-10
96/100 stars
Images
Related Articles
Software:Article Title: Rapid Detection of Senescent Mesenchymal Stromal Cells by a Fluorescent Probe. Article Snippet: This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record.. Please cite this article as doi: 10.1002/biot.201800691.. This article is protected by copyright. Article Title: Middle Level IM–MS and CIU Experiments for Improved Therapeutic Immunoglobulin Subclass Fingerprinting Article Snippet: .. Samples were eluted with a constant flow rate of 250 μL/min and using a chromatographic gradient from 10 to 25% B over 9 minutes, followed by a shallow gradient up to 27.8% B over 7 min. Then, the gradient increased up to 29.8% B over 1 minute, followed by 29.8 – 50% B over 2 minutes. nrCE-SDS analysis IgGs were analyzed in non-reduced condition using a MauriceTM system (Protein Simple) equipped with the Article Title: Flow-enhanced priming of hESCs through H2B acetylation and chromatin decondensation. Article Snippet: .. Data were analyzed using Article Title: Biodistribution of mRNA COVID-19 vaccines in human breast milk. Article Snippet: The proteins of interest were assayed with rabbit monoclonal antibody detection as described above, and the signal was detected using the Anti-Rabbit Detection Module (ProteinSimple DM001). .. Data were analyzed using Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma. Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense machine (ProteinSimple, San Jose, CA) in accordance with the manufacturer's protocols and as previously described.20,21 The primary antibodies used in the study were: mouse monoclonal DO-11 (BioRad; MCA1704, aa 181–190), whose epitope is present in the common region DBD and allows detection of all p53 protein isoforms; mouse monoclonal DO-1 (Santa Cruz Biotechnology; sc-126, aa 11–25), whose epitope is situated in the transactivation domain 1 that is present only in the TAp53α, TAp53β, and TAp53γ protein isoforms; rabbit polyclonal anti-p53 A300-249A-T (Bethyl Laboratories, Inc.; aa 375–393), which is specific to the α isoforms (TAp53α, Δ40p53α, Δ133p53α, and Δ160p53α); and anti-GAPDH (Cell Signaling; rabbit mAb #2118), which was used as the endogenous control. .. The rabbit polyclonal KJC8 antibody, which is specific to the β isoforms (TAp53β, Δ40p53β, Δ133p53β, and Δ160p53β), was provided by Prof. J-C. Bourdon (aa 331–341).7 All protein data were analyzed with Article Title: Expression profile of Bcl‐2 family proteins in newly diagnosed multiple myeloma patients Article Snippet: CNIA was performed using the WES system (ProteinSimple) according to the manufacturer's protocols and as previously outlined., , The primary antibodies used in this study were as follows: Bcl‐2 (sc‐7382), Bcl‐xL (54H6 Rabbit mAb #2764), Mcl‐1 (D35A5 Rabbit mAb #5453), Bax (D2E11 Rabbit mAb #5023), Bak (D4E4 Rabbit mAb #12105), Bim (C34C5 Rabbit mAb #2933), Puma (D30C10 Rabbit mAb #12450), Bad (D24A9 Rabbit mAb #9239), and Gapdh (14C10 Rabbit mAb #2118) proteins, the latter being used as the endogenous control. .. All protein data were analyzed and quantified with Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma Article Snippet: .. All protein data were analyzed with Expressing:Article Title: Rapid Detection of Senescent Mesenchymal Stromal Cells by a Fluorescent Probe. Article Snippet: This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record.. Please cite this article as doi: 10.1002/biot.201800691.. This article is protected by copyright. Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma. Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense machine (ProteinSimple, San Jose, CA) in accordance with the manufacturer's protocols and as previously described.20,21 The primary antibodies used in the study were: mouse monoclonal DO-11 (BioRad; MCA1704, aa 181–190), whose epitope is present in the common region DBD and allows detection of all p53 protein isoforms; mouse monoclonal DO-1 (Santa Cruz Biotechnology; sc-126, aa 11–25), whose epitope is situated in the transactivation domain 1 that is present only in the TAp53α, TAp53β, and TAp53γ protein isoforms; rabbit polyclonal anti-p53 A300-249A-T (Bethyl Laboratories, Inc.; aa 375–393), which is specific to the α isoforms (TAp53α, Δ40p53α, Δ133p53α, and Δ160p53α); and anti-GAPDH (Cell Signaling; rabbit mAb #2118), which was used as the endogenous control. .. The rabbit polyclonal KJC8 antibody, which is specific to the β isoforms (TAp53β, Δ40p53β, Δ133p53β, and Δ160p53β), was provided by Prof. J-C. Bourdon (aa 331–341).7 All protein data were analyzed with Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma Article Snippet: .. All protein data were analyzed with Western Blot:Article Title: Rapid Detection of Senescent Mesenchymal Stromal Cells by a Fluorescent Probe. Article Snippet: This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process, which may lead to differences between this version and the Version of Record.. Please cite this article as doi: 10.1002/biot.201800691.. This article is protected by copyright. Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma. Article Snippet: See the T erm s and C onditions (https://onlinelibrary.w iley.com /term s-and-conditions) on W iley O nline L ibrary for rules of use; O A articles are governed by the applicable C reative C om m ons L icense machine (ProteinSimple, San Jose, CA) in accordance with the manufacturer's protocols and as previously described.20,21 The primary antibodies used in the study were: mouse monoclonal DO-11 (BioRad; MCA1704, aa 181–190), whose epitope is present in the common region DBD and allows detection of all p53 protein isoforms; mouse monoclonal DO-1 (Santa Cruz Biotechnology; sc-126, aa 11–25), whose epitope is situated in the transactivation domain 1 that is present only in the TAp53α, TAp53β, and TAp53γ protein isoforms; rabbit polyclonal anti-p53 A300-249A-T (Bethyl Laboratories, Inc.; aa 375–393), which is specific to the α isoforms (TAp53α, Δ40p53α, Δ133p53α, and Δ160p53α); and anti-GAPDH (Cell Signaling; rabbit mAb #2118), which was used as the endogenous control. .. The rabbit polyclonal KJC8 antibody, which is specific to the β isoforms (TAp53β, Δ40p53β, Δ133p53β, and Δ160p53β), was provided by Prof. J-C. Bourdon (aa 331–341).7 All protein data were analyzed with Article Title: Expression of p53 protein isoforms predicts survival in patients with multiple myeloma Article Snippet: .. All protein data were analyzed with |