TetraSpeck™ Microspheres, 1.0 μm, fluorescent blue/green/orange/dark red
TetraSpeck™ Microspheres, 1.0 μm, fluorescent blue/green/orange/dark red
Invitrogen™

TetraSpeck™ Microspheres, 1.0 μm, fluorescent blue/green/orange/dark red

1.0 µm TetraSpeck™ミクロスフェアはすべて、4種類の蛍光色素(360/430nm(青)、505/515nm(緑詳細を見る
製品番号(カタログ番号)数量
T72820.5 mL
製品番号(カタログ番号) T7282
価格(JPY)
45,300
온라인 행사
Ends: 27-Mar-2026
75,500
割引額 30,200 (40%)
0.5 mL
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数量:
0.5 mL
1.0 µm TetraSpeck™ミクロスフェアはすべて、4種類の蛍光色素(360/430nm(青)、505/515nm(緑)、560/580nm(オレンジ)、660/680nm(ダークレッド))で染色され、それぞれが4つの適切に分離された励起ピークと発光ピークを表示するビーズを生じます。これらのミクロスフェアにより、特にマルチカラーでの使用について、科学的イメージングと商業的イメージングの両方に対し、従来の蛍光顕微鏡、共焦点レーザースキャン顕微鏡、関連する画像処理装置の校正を非常に容易に行うことができます。

当社の顕微鏡校正試薬の全コレクションを見る›

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
校正タイプ共焦点顕微鏡キャリブレーション、蛍光顕微鏡キャリブレーション
フォーマット懸濁液ビーズ
製品ラインTetraSpeck
数量0.5 mL
出荷条件室温
オレンジ、暗赤色、青、緑, Dark Red, Blue, Green
直径(メートル法)1 μm
製品タイプミクロスフェア
Unit Size0.5 mL
組成および保存条件
冷蔵庫(2℃~8℃)に保存し、遮光してください。

引用および参考文献 (16)

引用および参考文献
Abstract
The cohesion protein ORD is required for homologue bias during meiotic recombination.
Authors:Webber HA, Howard L, Bickel SE
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 ... More
Exocytosis of IgG as mediated by the receptor, FcRn: an analysis at the single-molecule level.
Authors:Ober RJ, Martinez C, Lai X, Zhou J, Ward ES
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 ... More
Quality assessment of confocal microscopy slide based systems: performance.
Authors:Zucker RM
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 ... More
Practical confocal microscopy and the evaluation of system performance.
Authors:Zucker RM, Price OT
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 ... More
Mast cell degranulation requires N-ethylmaleimide-sensitive factor-mediated SNARE disassembly.
Authors:Puri N, Kruhlak MJ, Whiteheart SW, Roche PA
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 ... More