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Citations & References (16)
Invitrogen™
TetraSpeck™ Fluorescent Microspheres Size Kit (mounted on slide)
このTetraSpeck蛍光ミクロスフェアサイズキットには、6つの視野領域を備えた1つの顕微鏡スライドが含まれています。5つの各視野領域に、1つのサイズのミクロスフェアが含まれています–（0.1、0.2、0.5、1.0、または4.0 µm詳細を見る
| 製品番号（カタログ番号） | 数量 |
|---|---|
| T14792 | 1 Kit |
製品番号（カタログ番号） T14792
価格（JPY）お問い合わせください ›
92,600
1 kit
数量:
1 Kit
このTetraSpeck蛍光ミクロスフェアサイズキットには、6つの視野領域を備えた1つの顕微鏡スライドが含まれています。5つの各視野領域に、1つのサイズのミクロスフェアが含まれています–（0.1、0.2、0.5、1.0、または4.0 µm）。残りの領域には、5種類のビーズサイズすべての混合物が含まれます。すべてのミクロスフェアは、励起ピークと発光ピークが適切に分離された4種類の蛍光色素（365⁄430 nm（青）、505⁄515 nm（緑）、560⁄580 nm（オレンジ）、660⁄680 nm（ダークレッド）で染色されます。InvitrogenのTetraSpeck™蛍光ミクロスフェアは、特にデコンボリューションに重要な点拡がり関数の導出や共局在化分析などのマルチカラーでの使用について、広視野、TIRF、および共焦点蛍光顕微鏡の校正に役立ちます。
当社の顕微鏡校正試薬の全コレクションを見る›
当社の顕微鏡校正試薬の全コレクションを見る›
研究用途にのみご使用ください。診断目的には使用できません。
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
フォーマットスライドに封入済み
製品ラインTetraSpeck
数量1 Kit
出荷条件室温
色オレンジ、暗赤色、青、緑, Dark Red, Blue, Green
直径（メートル法）0.5 μm、0.2 μm、0.1 μm、4 μm、1 μm
製品タイプFluorescent Microspheres Size Kit
Unit Size1 kit
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）
What are the excitation/emission peaks for TetraSpeck Microspheres?
The TetraSpeck Microspheres (Cat. Nos. T7279, T7280, T7281, T7283, T7284, T14792) are stained throughout with four different fluorescent dyes, yielding beads that each display four well-separated excitation/emission peaks at 360/430 nm (blue), 505/515 nm (green), 560/580 nm (orange) and 660/680 nm (dark red).
TetraSpeck Blue Dye Spectra
Fluorescence excitation and emission spectra of bead encapsulated TetraSpeck blue dye.
TetraSpeck Orange Dye Spectra
TetraSpeck Green Dye Spectra
TetraSpeck Dark Red Dye Spectra
Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.
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.
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
Colocalization of fluorescent markers in confocal microscope images of plant cells.
Journal:Nat Protoc
PubMed ID:18388944
'This protocol describes the steps needed to perform quantitative statistical colocalization on two-color confocal images, specifically of plant cells. The procedure includes a calibration test to check the chromatic alignment of the confocal microscope. A software tool is provided to calculate the Pearson and Spearman correlation coefficients (''Pearson-Spearman correlation colocalization''
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
Three-dimensional random access multiphoton microscopy for functional imaging of neuronal activity.
Journal:Nat Neurosci
PubMed ID:18432198
The dynamic ability of neuronal dendrites to shape and integrate synaptic responses is the hallmark of information processing in the brain. Effectively studying this phenomenon requires concurrent measurements at multiple sites on live neurons. Substantial progress has been made by optical imaging systems that combine confocal and multiphoton microscopy with