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引用和文献 (16)
Invitrogen™
TetraSpeck™ 微球，1.0 μm，蓝/绿/橙/深红色荧光
使用四种不同的荧光染料对1.0 μm TetraSpeck™ 微球进行染色，得到的每个微珠的激发/发射峰完全分开 - 360/430 nm（蓝色）、505/515了解更多信息
| 货号 | 数量 |
|---|---|
| T7282 | 0.5 mL |
货号 T7282
价格（CNY)
4,586.00
0.5 mL
数量:
0.5 mL
价格（CNY)
4,586.00
0.5 mL
使用四种不同的荧光染料对1.0 μm TetraSpeck™ 微球进行染色，得到的每个微珠的激发/发射峰完全分开 - 360/430 nm（蓝色）、505/515 nm（绿色）、560/580 nm（橙色）和660/680 nm（深红色）。这些微球可以极大地方便常规荧光显微镜，共聚焦激光扫描显微镜以及相关的图像处理设备的校准，以进行科学和商业成像（特别是多色应用）。
查看我们的全套显微镜校准试剂 ›
查看我们的全套显微镜校准试剂 ›
仅供科研使用。不可用于诊断程序。
规格
校准类型共聚焦显微镜校准、荧光显微镜校准
产品规格悬浮微珠
产品线TetraSpeck
数量0.5 mL
运输条件室温
颜色橙色、深红色、蓝色、绿色, Dark Red, Blue, Green
直径（公制）1 μm
产品类型微球
Unit Size0.5 mL
内容与储存
在冰箱（2°C 至 8°C）中避光储存。
引用和文献 (16)
引用和文献
Abstract
The cohesion protein ORD is required for homologue bias during meiotic recombination.
Journal:J Cell Biol
PubMed ID:15007062
'During meiosis, sister chromatid cohesion is required for normal levels of homologous recombination, although how cohesion regulates exchange is not understood. Null mutations in orientation disruptor (ord) ablate arm and centromeric cohesion during Drosophila meiosis and severely reduce homologous crossovers in mutant oocytes. We show that ORD protein localizes along
Exocytosis of IgG as mediated by the receptor, FcRn: an analysis at the single-molecule level.
Journal:Proc Natl Acad Sci U S A
PubMed ID:15258288
'IgG transport within and across cells is essential for effective humoral immunity. Through a combination of biochemical and in vivo analyses, the MHC class I-related neonatal Fc receptor (FcRn) is known to play a central role in delivering IgGs within and across cells. However, little is known about the molecular
Quality assessment of confocal microscopy slide based systems: performance.
Journal:Cytometry A
PubMed ID:16807897
'BACKGROUND: All fluorescence slide-based cytometry detections systems basically include the following components: (1) an excitation light source, (2) intermediate optics, and (3) a detection device consisting of a CCD camera or a PMT. The optical principles employed is slide-based systems are similar to those of confocal microscopes (CLSM). METHODS: The
Practical confocal microscopy and the evaluation of system performance.
Journal:Methods
PubMed ID:10491274
'The laser scanning confocal microscope has enormous potential in many fields of biology. Currently there is a subjective nature in the assessment of a confocal microscope''s performance by primarily evaluating the system with a specific test slide provided by the user''s laboratory. To achieve better performance from the equipment, it
Mast cell degranulation requires N-ethylmaleimide-sensitive factor-mediated SNARE disassembly.
Journal:J Immunol
PubMed ID:14607937
'Mast cells possess specialized granules that, upon stimulation of surface FcR with IgE, fuse with the plasma membrane, thereby releasing inflammatory mediators. A family of membrane fusion proteins called SNAREs, which are present on both the granule and the plasma membrane, plays a role in the fusion of these granules