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Sona sCMOS

Sona は、Andor 最新の高性能 sCMOS カメラプラットホームで、蛍光顕微鏡用に特化して設計されました。この度発売を開始した Sona 4.2B-11、Sona 2.0B-11 の両モデルは、いずれも背面照射型で量子効率 (QE) 95%、真空冷却による冷却温度は業界トップの -45 °C を実現しました。

  • QE 95%、冷却温度 -45 °C: 超高感度背面照射 sCMOS を採用

  • 4.2 メガピクセル (Sona 4.2B) : 細胞や全胚を広視野で捕捉

  • 70 fps フルフレーム: ダイナミックプロセスにもスメアなく追随可能

  • リニアリティ 99.7% 以上 : ダイナミックレンジ全域にわたり最高の定量精度

  • 長期の真空度保持および品質確保: センサ表面の湿気ゼロ、QE劣化なし


お問い合わせ

Sonaは、Andor社最新の高性能sCMOSカメラプラットホームで、特に蛍光顕微鏡用に設計されました。この度発売を開始したSona 4.2B-11、Sona 2.0B-11の両モデルは、いずれも背面照射型で量子効率 (QE) 95%、真空冷却による冷却温度は業界トップの -45 °Cを実現しました。

sCMOS感度を究極化するというAndor独自の技術によって、例え励起出力が低下した場合においても蛍光顕微鏡のSN比を最適化させることを可能としました。その結果、測定時間が延長した場合も生細胞が保存されます。またSonaの感度が極めて高いことも蛍光色素分子濃度の低下に対して有利に作用し、細胞の生理機能の混乱が最小限に抑えられます。感度が上がるということはすなわち露光時間を短くできるということであり、細胞内の信号伝達メカニズムや細胞運動性のようなダイナミックプロセスに対してより高いフレームレートでの測定を可能としました。ダイナミックレンジを拡げる「デュアルオペレーショナルアンプリファイア」法は、神経細胞のような難易度の高いサンプルの高精度のイメージングおよび定量化に最適な手法です。さらには、このクラス最高の定量精度を達成するため、Andorは搭載ソフトウェアの強化にも取り組みました。その結果、ダイナミックレンジ全域にわたり 99.7% を超え、市場をリードするリニアリティを実現しました。

フラッグシップモデルである 4.2 メガピクセル Sona 4.2B-11 は、2048 x 2048 ピクセル全域に有効なアクセスを可能とする独自の技術を駆使して、画期的な 32 mm 対角センサを導入しました。その結果、顕微鏡サイドが利用可能な視野全域がシステム全体の視野となりました。これは情報量の最大化が求められるアプリケーションに最適な特性であり、細胞、全胚、細胞組織のサンプルを完ぺきな明瞭さで、かつ大きな視野で取得することができます。

Sona 4.2B-11の視野に関する優位性: 2048 x 2048 ピクセル Sona 4.2B-11 は、1608 x 1608 ピクセル背面照射 sCMOS カメラよりも視野が 62% 広くなります。画像は、60x 対物レンズと組込み型 1.5x チューブレンズを装着した Nikon Ti2 顕微鏡を使って取得したもので、Nyquist 解像鮮明度を維持しながら 2048 x 2048 のピクセル全域にアクセスができています。 各種の顕微鏡ポートに Andor マグニファイングカプラユニット(MCU)を装着することによって増倍効果を付加するという選択肢にもご注目ください。

  • Sona 4.2B-11 (4.2メガピクセル) には標準品としてFマウントアタッチメントが付属していますが、当社は、柔軟性を最大にするためCマウントカップリングも提供しています(オプション)。カップリングの交換は簡単で、1400 x 1400(2メガピクセル)までのROIサイズに対応可能です。
  • Sona 2.0B-11 (2 メガピクセル) はCマウント専用で、各種顕微鏡の最大22 mmまでのCマウントポートに対応可能です。このモデルの 1400 x 1400 フルピクセルは、22 mm新型Cマウントポートを前提に設計されており、この共通マウントポートを介して利用可能な視野を最大化するものです。ただしセンターを合わせたROIを予め準備しておき、より小さな顕微鏡ポートに直接装着することも可能です。

Sona は、真空背面照射sCMOSプラットホームとしては唯一のものです。ノイズレベルの超最小化の実現もさることながら、性能の長寿命化という成果をもたらしたセンサ真空筐体に関するAndorの技術力も見逃さないでください。もし筐体による保護が不完全であれば、背面照射型のシリコンセンサは、湿気、炭化水素およびその他のガス汚染物質からの腐食作用の影響を受けやすく、QEの低下を含む性能の経年劣化が起こります。 Andorの知的財産 UltraVacTM プロセスの要素技術である密閉真空シールは、外気からのいかなる気体および湿気の侵入も阻止します。それによってセンサ表面の結露が防止されます。修理のために工場に持ち帰る必要もありません。

95% QE & lowest noise - Prolonged live cell observations / measure accurate physiology

4.2 Megapixel & 32 mm F-mount (Sona 4.2B-11) - Capture maximum field of cells and large tissue samples

2.0 Megapixel and 22 mm C-mount (Sona 2.0B-11) - Ideal for modern microscopes that have C-mount ports up to 22 mm

Easily adaptable to 60x and 40x objectives - Combine with Magnifying Coupler Unit (MCU) - preserve optical clarity over a range of sample types.

Vacuum Cooled to -45 °C - Very weak signals require lowest noise floor: Don’t be limited by camera thermal noise!

The ONLY vacuum back-illuminated sCMOS - Andor's proprietary UltraVac™ technology protects the sensor from (a) QE degradation, and (b) moisture condensation.

Anti-Glow Technology - Allows access to full 4.2 Megapixel array with long exposures – maximize field of view and sensitivity advantages.

48 fps (4.2 Megapixel); 70 fps (2.0 Megapixel) - Image highly dynamic samples without signal smear - e.g. cell motility, membrane dynamics, ion flux, blood flow.

Extended Dynamic Range mode - 'One snap quantification' across a 53,000:1 signal range - measure challenging samples such as neurons

> 99.7% linearity - Market leading quantitative accuracy over the whole signal range – confidence of measurement in any application where signal intensity indicates local concentration.

User configurable ROI - Adapt to a range of microscope port sizes. Push frame rates and save data storage space.

Fan and Water cooling as standard - Water cooling for maximum sensitivity and highly vibration sensitive set-ups, e.g. super-resolution and electrophysiology

USB 3.0 (USB 3.1 Gen 1) - A convenient high speed interface

Most Sensitive Back-illuminated sCMOS

Sona 4.2B-11 and Sona 2.0B-11 back-illuminated sCMOS models each feature 95% Quantum Efficiency (QE) and market-leading vacuum cooling to -45°C.

The darkcurrent of GPixel sCMOS sensors is relatively high, compared to that of BAE/Fairchild Imaging sCMOS sensors that are utilized in Zyla and Neo sCMOS cameras. This places additional emphasis on the need to deep cool the sensor in order to suppress the noise floor, i.e. minimizing the camera detection limit. Due to the unique vacuum design, Sona thermoelectrically cools to -25°C using only the internal fan for heat dissipation. Furthermore, Sona can utilize liquid assisted cooling to push down to a hugely competitive -45°C!

"Back-illuminated sensors are valued specifically for their enhanced sensitivity – it makes sense to choose the most sensitive adaption of this high-end technology."

Having the most sensitive Back-illuminated sCMOS camera carries a host of practical advantages within fluorescence microscopy:

  • Reduced laser illumination intensity - keep cells alive throughout study (i.e. suppressing phototoxic effects) and also limit dye photobleaching
  • Reduced fluorophore concentrations - maintaining accurate physiology in living specimens
  • Lower exposure times - follow faster processes
  • Better SNR with TIRF and confocal low light modalities - better image clarity with techniques that reject out of focus photons.

Anti-Glow: Accessing the Entire Sensor Array

The GSense400 back-illuminated sensor from GPixel is widely recognised to suffer from glow at the edges of the sensor. This glow manifests as false signal and is exposure dependent. To date, the effect has forced camera manufacturers to either limit the usable region of the sensor to an array size notably smaller than the native 2048 x 2048 full resolution, or alternatively to impose a severe 30 millisecond restriction on the maximum exposure length that is permitted by the camera. Either way this fundamentally restricts performance and usefulness across a range of applications, either through field of view limitation or through sensitivity limitation.

Andor have studied and characterised this sensor issue in detail and have developed and implemented a unique anti-glow technology to tackle this problem. The figure below shows a dark image of the GSense 400 back-illuminated sensor with and without anti-glow technology – the difference it makes is stark and has enabled Andor to open up the full 2048 x2048 array, while also allowing exposure times up to 20 seconds.

Magnifying Coupler Unit (MCU)

Andor provide an optional Magnifying Coupler Unit (MCU) accessory which can be used alongside the Sona 4.2B-11 in order to utilize the full field of view of this large sensor with several common types of modern research fluorescence microscopes.  It can be used to adapt both Sona 4.2B-11 or Sona 2.0B-11 for use with 60x and 40x objectives, thus increasing the on-sample field of view while also maintain Nyquist resolving clarity. Since the image is being 2x magnified onto a 32 mm diameter sensor area, then the MCU can be attached to any port that offers an image output of 16 mm or greater. This describes the vast majority of available ports. 

For further details, please refer to the specification sheet for the Andor Magnifying Coupler Unit

Extended Dynamic Range and Superb Linearity

The innovative Dual Amplifier architecture of sCMOS sensors uniquely circumvents the need to choose between high or low gain amplifiers, in that signal can be sampled simultaneously by both high gain (low noise) and low gain (high capacity) amplifiers. As such, the lowest noise of the sensor can be harnessed alongside the maximum well depth, affording widest possible dynamic range. Uniquely for such a relatively small pixel design, this allows for dynamic range performance of 53,000:1 in Sona.

Furthermore, on-camera intelligence delivers a significant linearity advantage, providing unparalleled quantitative measurement accuracy of > 99.7% across the full dynamic range. This provides measurement confidence in any application where signal intensity indicates local concentration, e.g. ion flux, FRET and expression analysis.

Fast Frame Rates

The Sona models are capable of delivering up to 70 fps, the data streaming to PC through a high-bandwidth USB 3.0 interface. This is ideal for fast applications such as cell motility, ion flux and blood flow imaging etc.

Faster speeds still are available through Region of Interest (ROI) selection, scaling only with ROI height, i.e. a full width ROI provides the same frame rate as a reduced with ROI, as long as they share the same number of rows. This can be useful for imaging elongated samples at fast frame rates, such as measuring calcium flux in smooth muscle cells.

The sCMOS sensors in Sona 4.2B-11 and Sona 2.0B-11-11 have highly parallel readout architecture, facilitating high data readout rates and therefore fast frame rates. All columns possess their own Amplifier and Analogue to Digital Converter (ADC), meaning that all columns are read out in parallel.

Rolling Shutter

The Sona 4.2B-11 and Sona 2.0B-11 cameras each utilize a Rolling Shutter exposure mechanism. Rolling shutter essentially means that different lines of the array are exposed at different times as the read out ‘wave’ sweeps through the sensor, a row at the bottom starting the exposure approximately 21 ms before rows at the sensor’s distal edge. The lowest readout noise and fastest frame rates are available from this mode. Rolling shutter only presents an issue when imaging relatively large, fast moving objects within the field. Then, aside from the risk of motion blur that can affect any imaging condition in which rate of motion is being temporally under-sampled, there is an additional possibility of rolling shutter spatial distortion. However, distortion is less likely when relatively small objects are moving at a rate that is being temporally oversampled by the frame rate, which in fact describes the vast majority of use cases.

A further potential downside of rolling shutter is that different regions of the exposed image will not be precisely correlated in time to other regions, which can be essential for some applications. For example, if a cell is electrically stimulated and it is important to measure the onset of calcium sparks relative to the stimulation event, then rolling shutter should not be used. In this case, a true global shutter mode is required, available in Zyla 5.5 and Neo 5.5 sCMOS cameras.

GPU Express

The Andor GPU Express library has been created to simplify and optimize data transfers from camera to a CUDA-enabled NVidia Graphical Processing Unit (GPU) card to facilitate accelerated GPU processing as part of the acquisition pipeline. GPU Express integrates easily with SDK3 for Andor sCMOS cameras, providing a user-friendly but powerful solution for management of high bandwidth data flow challenges; ideal for data intensive applications such as Light Sheet Microscopy, Super-Resolution Microscopy and Adaptive Optics.

  • Enhanced convenience, afforded by simple, optimized GPU data managemen
  • Guaranteed optimal data throughout
  • Superb, easily accessible documentation and examples.

Spurious Noise Filter

Andor’s Sona sCMOS camera comes equipped with an in-built FPGA filter that operates in real time to reduce the frequency of occurrence of high noise pixels. This real time filter corrects for pixels that would otherwise appear as spurious ‘salt and pepper’ noise spikes in the image.

The appearance of such noisy pixels is analogous to the situation of Clock Induced Charge (CIC) noise spikes in EMCCD cameras, in that it is due to the fact that we have significantly reduced the noise in the bulk of the sensor that the remaining small percentage of spuriously high noise pixels can become an aesthetic issue. The filter employed dynamically identifies such high noise pixels and replaces them with the mean value of the neighbouring pixels.

Hardware Timestamp

The Sona platform can generate a timestamp for each image that is accurate to 25 ns. Accurate timestamps can be important where precise knowledge of frame time impacts temporal dynamic analysis. This is especially important for fast events, where computer and interface latencies need to be considered. Areas include signalling cascades, vesicle trafficking, lipid dynamics, synaptic re-modelling, action potential studies using opto-genetics and opto-physiology. Timestamps can also be useful for FRAP Analysis, facilitating the estimation of diffusion rates

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