BioConfirm 軟件
Agilent MassHunter BioConfirm 軟件能夠通過簡(jiǎn)便易用的工作流程對(duì)生物分子進(jìn)行常規(guī)表征,適用于寡核苷酸分析、完整蛋白質(zhì)分析、肽譜分析和常規(guī)寡糖分析。這款用于 LC/Q-TOF 的生物制藥軟件是生物制藥產(chǎn)品(如單克隆抗體和寡核苷酸)質(zhì)譜分析全面解決方案的重要組成部分。借助先進(jìn)的安全功能和內(nèi)置的技術(shù)控制,BioConfirm 網(wǎng)絡(luò)化工作站能夠盡可能降低安全風(fēng)險(xiǎn),同時(shí)有助于保持?jǐn)?shù)據(jù)可靠性。
從自動(dòng)化樣品前處理到分離和檢測(cè)再到數(shù)據(jù)分析和報(bào)告,安捷倫生物制藥工作流程可提供先進(jìn)的分析。藥物/抗體比率 (DAR) 計(jì)算器、靈活的報(bào)告模板等工具以及與 MassHunter WalkUp 的集成操作,使非專家也能利用專業(yè)的 LC/MS 功能。
從自動(dòng)化樣品前處理到分離和檢測(cè)再到數(shù)據(jù)分析和報(bào)告,安捷倫生物制藥工作流程可提供先進(jìn)的分析。藥物/抗體比率 (DAR) 計(jì)算器、靈活的報(bào)告模板等工具以及與 MassHunter WalkUp 的集成操作,使非專家也能利用專業(yè)的 LC/MS 功能。
- Data Analysis
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Product Details
Features
- 滿足數(shù)據(jù)可靠性標(biāo)準(zhǔn),提供技術(shù)控制確保遵循 FDA 21 CFR Part 11、歐盟附錄 11、GAMP 5、ISO/IEC 17025 和 EPA 40 CFR Part 160 法規(guī)合規(guī)性指南的實(shí)驗(yàn)室安全地采集、處理、報(bào)告和存儲(chǔ)數(shù)據(jù)
- 對(duì)于寡核苷酸的表征,可以使用自定義的結(jié)構(gòu)單元、連接子和修飾快速設(shè)置雜質(zhì)分析和序列確認(rèn)工作流程
- 對(duì)于完整蛋白質(zhì)分析,能夠?qū)ν暾鞍踪|(zhì)數(shù)據(jù)進(jìn)行快速解卷積,以確定分子量并確認(rèn)翻譯后修飾 (PTMs)
- 對(duì)于肽譜分析,可靠地執(zhí)行序列確認(rèn),并使用我們的序列覆蓋圖同時(shí)審查多個(gè)樣品(例如,不同的消化酶)
- 游離寡糖工作流程依賴于優(yōu)化的寡糖數(shù)據(jù)庫,可輕松進(jìn)行分析設(shè)置,并且適用于多種商業(yè)和定制標(biāo)簽
- MassHunter WalkUp 使樣品提交人員無需成為液質(zhì)聯(lián)用專家即可利用專業(yè) LC/MS 功能
Specifications
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| 當(dāng)前軟件版本 |
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| 支持的數(shù)據(jù)管理 |
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| 支持的附加軟件 |
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Technology
Applications
Literature
- Key Literature
-
Agilent MassHunter BioConfirm Software Brochure
BioConfirm Software- Rapid Characterization of Protein Biopharmaceuticals.
- Brochures
- English
- 19 May 2022
- 1.41 MB
Ensuring Regulatory Compliance and Data Integrity with MassHunter Software Solutions
A technical overview of the compliance features for LC/TOF and LC/Q-TOF.
- Technical Overviews
- English
- 15 Oct 2021
- 1.34 MB
- Application Notes
- Brochures
- Flyers
- Posters
- Technical Overviews
- White Papers
Support
- Quick Reference Guides
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MassHunter BioConfirm 12.0 Quick Start Guide
This guide provides instructions for installing and using MassHunter BioConfirm 12.0.
- Quick Reference Guides
- English
- 02 Nov 2022
- 11.80 MB
- Revision Tables
- User Manuals
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Tools
Videos
Training & Events
Meet regulatory compliance for biopharma with new mass spec software solutions
Data integrity plays a key role in ensuring the quality and safety of biopharmaceutical products. In this webinar, explore the current regulatory landscape and how new mass spectrometry software updates can enable you to address data integrity and meet regulatory requirements, such as US FDA 21 CFR Part 11 and EU Annex 11. Learn how advanced security features and built-in technical controls minimize security risks when applied to workflows for the analysis of intact proteins, protein digests and released glycans, by enabling setup of user roles, user permissions, audit trails, checksums, and secure content management across all software modules.
Webinar/Training
安捷倫培訓(xùn)
安捷倫培訓(xùn)中心提供多種培訓(xùn)學(xué)習(xí)選項(xiàng),幫助您提高技能與實(shí)驗(yàn)室效率。
Location:
在線培訓(xùn)
Date: 2021 年 8 月 15 日
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