Flow Cytometry Size Calibration Kit (nonfluorescent microspheres)
Flow Cytometry Size Calibration Kit (nonfluorescent microspheres)
Invitrogen™

Flow Cytometry Size Calibration Kit (nonfluorescent microspheres)

当社のフローサイトメトリーサイズキャリブレーションキットには非蛍光の粒子サイズキャリブレーション標準が含まれており、フローサイトメトリーによる細胞サイズの測定を簡単かつ正確に行うことができます。このキットには、次の直径の、非常に均一なポリスチレンミクロスフェアの6つの懸濁液が含まれています。1.0 μm, 2.0 μm, 4.0詳細を見る
製品番号(カタログ番号)数量
F138381キット
製品番号(カタログ番号) F13838
価格(JPY)
96,800
Each
お問い合わせください ›
数量:
1キット
当社のフローサイトメトリーサイズキャリブレーションキットには非蛍光の粒子サイズキャリブレーション標準が含まれており、フローサイトメトリーによる細胞サイズの測定を簡単かつ正確に行うことができます。このキットには、次の直径の、非常に均一なポリスチレンミクロスフェアの6つの懸濁液が含まれています。1.0 μm, 2.0 μm, 4.0 μm, 6.0 μm, 10.0 μm, 15.0 μm。

フローサイトメトリーキャリブレーションおよびサイズ参照ビーズに関する追加情報を見る。
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
検出法散乱
直径(メートル法)1、2、4、6、10、15
励起波長域非蛍光
使用対象 (装置)フローサイトメーター
フォーマット懸濁
数量1キット
出荷条件室温
使用対象(アプリケーション)フローサイトメトリー
製品タイプフローサイトメトリーサイズキャリブレーションキット
Unit SizeEach
組成および保存条件
高均一性ポリスチレンミクロスフェアのバイアル 6 本入り:直径1.0 μm、2.0 μm、4.0 μm、6.0 μm、10 μm、15 μmのミクロスフェア。
  • 冷蔵庫に2~8℃で保存
  • よくあるご質問(FAQ)

    What is the Flow Cytometry Size Calibration Kit (Cat. No. F13838) used for?

    Our Flow Cytometry Size Calibration Kit has non-fluorescent particle-size calibration standards that provide a simple, accurate way to determine cell sizes by flow cytometry. The kit contains six suspensions of highly uniform polystyrene microspheres with the following diameters: 1.0 µm, 2.0 µm, 4.0 µm, 6.0 µm, 10.0 µm and 15.0 µm. All of the microsphere suspensions are provided in convenient dropper vials. This kit looks at the scatter properties of non-fluorescent microspheres of known sizes to determine approximate cell sizes.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    What is the smallest size that I can detect with the Attune NxT Acoustic Focusing Cytometer?

    The smallest size that you can detect with the Attune NxT Acoustic Focusing Cytometer is 0.5 µm.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    What is the Attune NxT Autosampler?

    The Attune NxT Autosampler, an optional accessory for the Attune NxT Acoustic Focusing Cytometer, enables rapid processing of up to 384 samples. It has broad compatibility with different plate formats, both 96- and 384-well plates. It has an intelligent probe designed to minimize clogging and carryover (<0.5%) and to prevent damage to the instrument. It mixes by aspiration rather than shaking to ensure homogeneity of the sample and maintain cell viability. Is performs automated cleaning as part of the shutdown process of the Attune NxT Cytometer. It provides consistent data regardless of sampling method (tube vs. plate) and collection rate.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    What are the advantages of acoustic-assisted hydrodynamic focusing in flow cytometry?

    -Modular design - Multiple configurations available - field upgradable.
    -Save time - 10X faster speeds with no loss in data quality.
    -Simplified sample prep - No wash, no lyse options, non-clogging fluidics.
    -Enables unique applications - Complex protocols on a broad range of cell types and samples.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    How is the Attune NxT Acoustic Focusing Cytometer different from traditional flow cytometers?

    With the option to be configured with up to 4 lasers and 14 colors for multi-parameter analysis the Attune NxT Acoustic Focusing Cytometer was designed as a modular system to fit most experimental needs and lab budgets. The novel design of the optical path helps ensure precise fixed alignment of four spatially separated lasers onto the sample stream enabling consistency in data over time, superior performance, and superior reliability. The instrument can be configured with up to 4 solid-state lasers (405 nm, 488 nm, 561 nm, and 637 nm) with flat top beam profiles.

    The Attune NxT Flow Cytometer's acoustic focusing uses ultrasonic radiation pressure (> 2 MHz) to transport particles into the center of the sample stream. This pre-focused stream is then injected into the sheath stream, which supplies an additional hydrodynamic pressure to the sample. The combination of these two forces- termed acoustic-assisted hydrodynamic focusing-results in a narrow core stream and uniform laser illumination, regardless of the sample input rate. In traditional cytometers that rely solely on hydrodynamic focusing, the sample core widens to accommodate the increases in flow rate, which results in less uniform laser light illumination.

    Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

    引用および参考文献 (2)

    引用および参考文献
    Abstract
    Preparation of genomic DNA from a single species of uncultured magnetotactic bacterium by multiple-displacement amplification.
    Authors:Arakaki A, Shibusawa M, Hosokawa M, Matsunaga T,
    Journal:Appl Environ Microbiol
    PubMed ID:20081000
    Magnetotactic bacteria comprise a phylogenetically diverse group that is capable of synthesizing intracellular magnetic particles. Although various morphotypes of magnetotactic bacteria have been observed in the environment, bacterial strains available in pure culture are currently limited to a few genera due to difficulties in their enrichment and cultivation. In order ... More
    Diabetic cardiomyopathy-associated dysfunction in spatially distinct mitochondrial subpopulations.
    Authors:Dabkowski ER, Williamson CL, Bukowski VC, Chapman RS, Leonard SS, Peer CJ, Callery PS, Hollander JM,
    Journal:Am J Physiol Heart Circ Physiol
    PubMed ID:19060128
    Diabetic cardiomyopathy is the leading cause of heart failure among diabetic patients, and mitochondrial dysfunction has been implicated as an underlying cause in the pathogenesis. Cardiac mitochondria consist of two spatially, functionally, and morphologically distinct subpopulations, termed subsarcolemmal mitochondria (SSM) and interfibrillar mitochondria (IFM). SSM are situated beneath the plasma ... More