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Citations & References (305)
Invitrogen™
Resazurin, Sodium Salt
非蛍光性の レザズリン は、フローサイトメトリー、蛍光顕微鏡、およびハイスループットスクリーニングによる細菌、酵母、真核生物などのさまざまな細胞における蛍光酸化還元インジケータとして使用できます。赤色蛍光製品であるレゾルフィンは、約575/585詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| R12204 | 10 mg |
製品番号（カタログ番号） R12204
価格（JPY）お問い合わせください ›
20,700
Online offer
Ends: 27-Mar-2026
34,500割引額 13,800 (40%)
Each
数量:
10 mg
非蛍光性の レザズリン は、フローサイトメトリー、蛍光顕微鏡、およびハイスループットスクリーニングによる細菌、酵母、真核生物などのさまざまな細胞における蛍光酸化還元インジケータとして使用できます。赤色蛍光製品であるレゾルフィンは、約575/585 nmの最大吸光／最大発光を示します。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
概要Resazurin, Sodium Salt
検出法蛍光
染色剤タイプSalt
形状固体
フォーマットTube
数量10 mg
出荷条件室温
色Red
Emission585
Excitation Wavelength Range575 nm
使用対象（アプリケーション）Viability Assay
使用対象 (装置)Microplate Reader
製品ラインInvitrogen
製品タイプResazurin
Unit SizeEach
組成および保存条件
室温で保存し、光から保護します。
よくあるご質問（FAQ）
How do alamarBlue reagent and PrestoBlue reagent differ from resazurin and C12-resazurin?
引用および参考文献 (305)
引用および参考文献
Abstract
Rapid screening of natural products for antimycobacterial activity by using luciferase-expressing strains of Mycobacterium bovis BCG and Mycobacterium intracellulare.
Journal:Antimicrobial agents and chemotherapy
PubMed ID:9055994
The object of this study was to investigate the ability of a rapid luciferase assay to detect antimycobacterial activity in plant extracts. Recombinant strains of Mycobacterium bovis BCG (rBCG) and Mycobacterium intracellulare expressing firefly luciferase were used as the test organisms. Assays were conducted in a 96-well minitube format under
Inhibition of growth and sensitization to cisplatin-mediated killing of ovarian cancer cells by polyphenolic chemopreventive agents.
Journal:J Cell Physiol
PubMed ID:12447990
'The polyphenolic compounds curcumin and quercetin increased sensitivity of ovarian cancer cells (CAOV3 and SKOV3) to cisplatin. The effect was obtained when the compounds were added simultaneously with cisplatin, as well as when they were added 24 h before. High serum levels of certain cytokines, for example interleukin-6 (IL-6), have
Mechanism of target cell recognition by natural killer cells: characterization of a novel triggering molecule restricted to CD3- large granular lymphocytes.
Journal:J Exp Med
PubMed ID:1720812
'In an attempt to identify a molecule in target recognition by CD3- large granular lymphocytes (LGL), we have generated a rabbit antiidiotypic (anti-ID) serum against a monoclonal antibody (mAb 36) that reacted with the cell membrane of K562. Flow cytometry analysis demonstrated that the anti-ID serum bound selectively to CD3-
Functional in vivo MHC class II loading by endogenously synthesized glycoprotein during viral infection.
Journal:J Immunol
PubMed ID:9190921
'MHC class II presentation of antigenic peptides derived from soluble proteins is usually preceded by antigenic uptake via (nonreceptor-mediated) endocytosis by professional APCs, followed by processing in endosomal compartments. Although in vitro alternative pathways for MHC class II loading have been described for certain intracellularly synthesized proteins, the importance of
Cell proliferation enhances entry of Listeria monocytogenes into intestinal epithelial cells by two proliferation-dependent entry pathways.
Journal:J Med Microbiol
PubMed ID:9511817
'Bacterial entry into intestinal host cells is the result of a fairly sophisticated manipulation of host cell machinery by the pathogens. To study further the potential cell target of Listeria spp., the in-vitro entry of L. monocytogenes strains into intestinal cells was examined in relation to the metabolism, proliferation and