REAfinity™ 重組抗體:高純度、低背景分析
透過創新的 Fc 區域工程技術,實現零背景信號的流式細胞術分析

解決流式細胞術背景信號問題
傳統抗體:高背景信號干擾
REAfinity™ 抗體:零背景信號
REAfinity™ recombinant 抗體透過特定突變的人類 IgG1 Fc 區域,完全去除與 "Fcγ receptor" 的結合能力,從根本上解決流式細胞術中的背景信號問題,提供更清晰、更準確的分析結果。
REAfinity™ 技術革新優勢
零背景信號設計
透過精密的 Fc 區域突變工程,完全消除 "Fcγ receptor binding",實現真正的零背景干擾,讓您的流式細胞術資料更加清晰準確。
標準化 Recombinant 製程
採用 "standardized mammalian expression system",確保每批次產品具有一致的高純度和穩定性,提升實驗結果的再現性。
One Universal Isotype Control
所有 REAfinity™ 抗體使用相同的人類 IgG1 "isotype control",大幅簡化實驗設計,降低成本並提高效率。
卓越品質保證
批次間一致性保證
REAfinity™ recombinant 抗體採用 "mammalian cell expression system" 製造,確保每個批次都具有相同的:
- 分子結構完整性
- 抗原結合親和力
- 螢光標記密度
- 功能活性穩定性

廣泛應用領域
學術研究
- 免疫學研究
- 細胞生物學
- 分子醫學
- 發育生物學
生物製藥
- 藥物開發
- 品質控制
- 生物製劑檢驗
- 療效評估
技術資源與文件
產品規格資訊
| 產品特性 | REAfinity™ 抗體 | 傳統抗體 |
|---|---|---|
| 背景信號 | 零背景 | 高背景 |
| Fc 受體結合 | 完全消除 | 存在結合 |
| 同型對照 | 單一通用 | 多種不同 |
| 批次一致性 | 極高 | 變異較大 |
備註:具體產品貨號請聯繫技術支援團隊,我們將根據您的實驗需求提供最適合的產品選擇。
常見問題解答
REAfinity™ Recombinant Antibodies: Superior Quality, Zero Background Analysis
REAfinity™ recombinant antibodies represent a groundbreaking advancement in flow cytometry analysis, engineered with specifically mutated human IgG1 Fc regions to completely eliminate Fcγ receptor binding and achieve true zero background signals. This innovative technology fundamentally solves the persistent background signal problems that have long plagued flow cytometry applications, delivering unprecedented clarity and accuracy in cellular analysis.
The cornerstone of REAfinity™ technology lies in its sophisticated Fc region engineering, where precise mutations are introduced to the human IgG1 framework to abolish any interaction with Fcγ receptors while maintaining optimal antigen binding characteristics. This revolutionary approach ensures that researchers can achieve crisp, clean data with minimal non-specific binding, particularly crucial when analyzing cell populations with high Fcγ receptor expression such as macrophages, dendritic cells, and B cells.
One of the most significant advantages of REAfinity™ antibodies is the implementation of a single, universal human IgG1 isotype control across the entire product range. This standardization dramatically simplifies experimental design, reduces costs, and eliminates the complexity of managing multiple isotype controls, allowing researchers to focus on their scientific objectives rather than experimental logistics.
