Ferhonox-1荧光染色
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Ferhonox-1荧光染色
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Web德尔塔生物为你提供钾、钙、锌、铁、钠、镁金属离子荧光探针简介。钾、钙、锌、铁、钠、镁金属离子荧光探针简介仅用于科研，不能用于人体治疗、药物开发、和其他商业用途。德尔塔生物一直致力于科研产品的研发以满足国内广大科研院校及其他相关科研单位的需求。 WebNational Center for Biotechnology Information
WebMay 23, 2024 · FeRhoNox-1在37℃，与Fe2+反应1h后，荧光明显增强。. 荧光峰约在575nm。. FeRhoNox-1，也称为RhoNox-1，是一种活跃的荧光探针，特异性检测不稳定的铁 (II)离子（Fe2+）。. 一旦与Fe2+反应后，不可逆的生成一种橙色（红色）荧光产物（Absmax=540nm，FLmax=575nm，图1.FeRhoNox-1的 ... http://www.rx-8.com/customized/113612.html
http://mito-bio.com/show_8433.aspx#:~:text=FeRhoNox%E2%84%A2-1%20%28also%20called%20as%20RhoNox-1%29%20is%20an%20activatable,tends%20to%20localize%20in%20Golgi%20within%20a%20cell.
WebJul 1, 2024 · FeRhoNox-1 stained cells were less suitable for this protocol, as the chemical dye targets undefinable intracellular regions. Thus, we exploited Perls stained cells, intensified with diaminobenzidine (DAB), and then correlated high-resolution bright-field and EM images of the same cells (Fig. 2 b and c).
WebRhoNox-1 is a fluorescent probe for the specific detection of divalent iron ions, and when RhoNox-1 reacts with Fe 2+. RhoNox-1 can generate an irreversible orange (red) … herbs rye happy hourWebFeRhoNox-1，也称为RhoNox-1，是一种活跃的荧光探针，特异性检测不稳定的铁(II)离子（Fe2+）。 一旦与Fe2+反应后，不可逆的生成一种橙色（红色）荧光产物（Absmax=540nm，FLmax=575nm，图1.FeRhoNox-1的 … herbs safe for cats indoorWebMay 16, 2024 · 特异性Fe2+荧光探针 FeRhoNoxTM-1. 该探针能够特异性地与高尔基体的Fe2+反应。. 能检测活细胞高尔基体的Fe2+. enceappears aroResponse of … matter in our surroundings practice questionsWebJul 13, 2024 · Followed by 12 h incubations, both BEAS-2B and alveolar macrophages were washed by PBS and stained by 10 μg/mL Hoechst 33342, 10 μg/mL FeRhoNox-1, and 20 μg/mL WGA in media for 1 h at 37 °C. herbs safe for breastfeedingWeb德尔塔生物为你提供CAS：1241962-11-7，BHQ-2 amine，BHQ-2 氨基可用于溶液相共轭。CAS：1241962-11-7，BHQ-2 amine，BHQ-2 氨基可用于溶液相共轭仅用于科研，不能用于人体治疗、药物开发、和其他商业用途。德尔塔生物一直致力于科研产品的研发以满足国内广大科研院校及其他相关科研单位的需求。 herbs safe during pregnancyWebm.cnreagent.com 扫一扫，直接在手机上打开 herbs rye restaurant las vegas nvWebAug 1, 2024 · Briefly, 1 × 10 6 IMR-32 cells were seeded in a 6-well plate 1 day before the experiment. The next day, cells were collected and centrifuged at 3,000 g for 5 minutes. The cells were washed with HBSS buffer and centrifuged at 3,000 g for 5 minutes. Collected cells were stained with 10 μM FeRhoNox-1 in HBSS for 30 minutes in a CO 2 incubator ... matter inputs of photosynthesis