alamarBlue^® 阿爾瑪藍（細胞增殖及毒性檢測試劑）

基本描述：

阿爾瑪藍（Alamar Blue）是一種細胞增殖檢測試劑，對各種人和哺乳動物細胞、細菌和真菌提供一種快速和敏感的細胞增殖和毒性檢測方法。

阿爾瑪藍（Alamar Blue）是一種基于刃天青（resazurin）的檢測試劑。刃天青作為一種一種氧化還原（REDOX）指示劑，根據(jù)細胞代謝還原情況發(fā)生顏色變化。氧化態(tài)的刃天青呈紫藍色且基本無熒光，其還原態(tài)產(chǎn)物試鹵靈（resorufin）轉變?yōu)榉奂t色且高度熒光，產(chǎn)生的熒光強度與呼吸活細胞數(shù)量呈正比。通過檢測呼吸過程中氧化水平，阿爾瑪藍用作一種定量檢測細胞活力和毒性的直接指示劑。阿爾瑪藍的顏色變化可通過普通分光光度計檢測吸光度變化，檢測波長為570nm，參考波長為600nm；阿爾瑪藍的熒光變化可通過熒光光度計檢測，激發(fā)波長在530~560nm之間，發(fā)射波長為590nm。

檢測原理：（細胞增殖實驗 Cell proliferation assay））

※ 生長中細胞引起Alamar Blue的化學還原反應；

※ 持續(xù)性細胞生長維持還原環(huán)境，使得Alamar Blue呈紅色，發(fā)強熒光；

※ 生長受抑制維持氧化環(huán)境，使得Alamar Blue呈藍色，無熒光；

※ 使用基于熒光或吸光值檢測的儀器收集數(shù)據(jù)；

※ 熒光檢測的激發(fā)波長為530~560nm之間，發(fā)射波長為590nm；

※ 吸光值檢測的波長為570nm，參考波長為600nm；

保存方法：

室溫12個月穩(wěn)定，2-8°C保存20個月穩(wěn)定；避光保存；

產(chǎn)品優(yōu)勢：

• 簡單：水溶性，只需添加和測量即可；
• 靈活：顯色和熒光檢測，懸浮細胞和貼壁細胞；
• 無毒：對細胞無毒，對使用者和環(huán)境也無毒；
• 可靠：大量引用用于細胞毒性和活力檢測；
• 規(guī)?；汉唵畏糯篌w系用于高通量分析
• 高靈敏：zui低可檢測到50個細胞
• 穩(wěn)定高：*緩沖配方使其能用于長期研究；
• 經(jīng)濟：不需要細胞裂解，使細胞能繼續(xù)培養(yǎng)用于后續(xù)分析；

訂購信息：品牌保證，現(xiàn)貨供應，大量使用文獻，國內(nèi)外上萬實驗室的認可品質(zhì)，咨詢，，：。

【注1】：按照96孔板，每孔100µl終體積來算，5ml alamarBlue^®可做500個孔；25ml可做2500個孔。

【注2】：alamarBlue^® Technical Datasheet

引用文獻（AbdSerotech alamarBlue^®，43篇）：

1. Lewis, C.S. et al. (2010) Local Antibiotic Delivery with Bovine Cancellous Chips.
2. Alsford, S. and Horn, D. (2011) Elongator Protein 3b Negatively Regulates Ribosomal DNA Transcription in African Trypanosomes.
3.  Crilly, A. et al. (2011) Phosphodiesterase 4 (PDE4) regulation of proinflammatory cytokine and chemokine release from rheumatoid synovial membrane.
4. Paget, C. et al. (2011) Potential Role of Invariant NKT Cells in the Control of Pulmonary Inflammation and CD8+ T Cell Response during Acute Influenza A Virus H3N2 Pneumonia.
5. Lakhkar, N. et al. (2011) Titanium and strontium-doped phosphate glasses as vehicles for strontium ion delivery to cells.
6. Wilson, B.A. et al. (2011) High-throughput screen identifies novel inhibitors of cancer biomarker a-methylacyl coenzyme A racemase (AMACR/P504S).
7. Lau, L.I. et al. (2011) The Effect of Photooxidative Stress and Inflammatory Cytokine on Complement Factor H Expression in Retinal Pigment Epithelial Cells.
8. Arlian, B.M. and Tinker, J.K. (2011) Mucosal Immunization with a Staphylococcus aureus IsdA-Cholera Toxin A2/B Chimera Induces Antigen-Specific Th2-Type Responses in Mice.
9. Voloshin, T. et al. (2011) G-CSF supplementation with chemotherapy can promote revascularization and subsequent tumor regrowth: prevention by a CXCR4 antagonist.
10. Rao, T.D. et al. (2011) Dual-Fluorescence Isogenic High-Content Screening for MUC16/CA125 Selective Agents.
11. Uitdehaag, J.C. et al. (2011) Multidimensional Profiling of CSF1R Screening Hits and Inhibitors: Assessing Cellular Activity, Target Residence Time, and Selectivity in a Higher Throughput Way.
12. Rzhepishevska, O. et al (2011) The antibacterial activity of ga3+ is influenced by ligand complexation as well as the bacterial carbon source.
13. Xu, S. et al. (2011) Marek's disease virus type 1 microRNA miR-M3 suppresses cisplatin-induced apoptosis by targeting Smad2 of the transforming growth factor beta signal pathway.
14.  Ardakani, A.G. et al. (2014) Quantifying the correlation between spatially defined oxygen gradients and cell fate in an engineered three-dimensional culture model.
15. Nakayama, G.R. et al. (1997) Assessment of the Alamar Blue assay for cellular growth and viability in vitro.
16. Diril, M.K. et al. (2012) Cyclin-dependent kinase 1 (Cdk1) is essential for cell division and suppression of DNA re-replication but not for liver regeneration.
17.  Warrier, T. et al. (2012) Antigen 85C inhibition restricts Mycobacterium tuberculosis growth through disruption of cord factor biosynthesis.
18. Dreidax, D. et al. (2013) Low p14ARF expression in neuroblastoma cells is associated with repressed histone mark status, and enforced expression induces growth arrest and apoptosis.
19. Wang, H. et al. (2014) Enhanced osteoblast responses to poly ether ether ketone surface modified by water plasma immersion ion implantation.
20. Park, K.H. et al. (2014) Expression of polysialylated neural cell adhesion molecules on adult stem cells after neuronal differentiation of inner ear spiral ganglion neurons.

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 — —Written/Edited by V. Shallan【版權歸MKBio懋康所有】
 

上海懋康生物科技有限公司是一家涉足于生命科學和生物技術領域研究的試劑、儀器和實驗室消耗品與實驗服務工作，主要從事細胞生物學、植物學、分子生物學、免疫學、生物化學、蛋白組學。生物制藥與診斷試劑研發(fā)生產(chǎn)等領域。 本公司秉承“以人為本，以誠為信、合同守信”的經(jīng)營理念。堅持"品質(zhì)保障"的原則為廣大客戶提供優(yōu)質(zhì)產(chǎn)品。