카테고리 보관물: 260611_repair

PE-300ultra

 

CoolLED pE-300ultra

 

NOW DOUBLE THE INTENSITY AT THE SAMPLE PLANE

CoolLED’s pE-300ultra is a fluorescence microscopy light source which offers intense, broad-spectrum LED illumination for imaging most common fluorescent stains.  Users have access to both microsecond switching via multiple TTL inputs and the ability to mount inline excitation filters.  This, when paired with today’s high performance multi band filter sets, facilitates imaging traditionally done via a white light source and a filter wheel, with all the benefits of LED.

 

The pE-300ultra is the most controllable member of the pE-300 Series.  In addition to the many features of the pE-300lite and the pE-300white, the system offers precise control over wavelength intensity and shuttering.  Until now these benefits have only been accessible to users of high end, highly flexible illuminators such as the CoolLED pE-4000.

Throughout 2017 we will be releasing exciting new products and product updates.  The first member of the CoolLED product range to receive the star treatment is the pE-300 Series.

As part of the award winning pE-300 Series, the NEW Enhanced pE-300ultra  now delivers DOUBLE the intensity at the microscope sample plane.  It allows adjustment of output in 1% steps, giving precise control.  The broad spectrum covers everyday fluorophores: DAPI, CFP, Aqua, FITC, TRITC, TxRed, Cy5 and many more.

It is now possible to view and image your samples brighter than ever.

Convaleria taken with Photometrics Prime camera with 10ms exposure.

 

LED illumination means no mercury to dispose of and lower energy costs due to low power consumption and the precise control offered. With the new enhanced pE-300ultra, all 3 channels at full power use just 46 Watts. That is almost a quadruple efficiency increase!

This compares to other LED technology that uses 120 to 350 Watts. This leap forward in technology makes LEDs more attractive when compared to old Mercury or Metal Halide technology.  Where “green” funding is available, the reduction in institutional energy usage improves the return on investment.

CoolLED’s pE-300 Series  was the 2017 winner of the “Go Beyond Award” in the “Products” category for “Excellence in sustainability in laboratory and other high technology facilities”  The International Institute for Sustainable Laboratories (I2SL) runs a unique awards program honouring organisations, individuals, products,and projects that are advancing sustainable, high-performance facilities.

The pE-300ultra  offers triggering from multiple TTL inputs which, coupled with the ability to mount inline excitation filters, provides microsecond switching of pre-filtered excitation light.  This, when paired with today’s high performance multi-band filter sets, facilitates imaging traditionally done using a white light source and a filter wheel, with all the benefits of LED, and most excitingly at speeds not previously so affordable.

The system comprises a pE-300ultra Light Source, Control Pod, set of three Excitation Filter Holders and Power Supply.  It can be specified with a microscope adaptor for direct fit configuration or with a 3mm diameter liquid light guide if there is a need to keep the source of illumination remote from the microscope.  An optional pE-Universal Collimator and microscope adaptor can be selected for use with a liquid light guide.

A benefit of the pE-300ultra is that  stains can be viewed either individually or in combination, without filter cube changes.  This makes it ideal for use with multi-band filter sets as the screening process can be simplified when fewer filter cubes are used.  Independent control of the three LED channels means that the user can control the level of excitation of each fluorescent stain independently on a multi-stained sample, potentially removing the need for single band filter sets altogether. For further information on improved multi-stain testing, go to the Downloads tab.

An important additional feature of the pE-300ultra is that it includes CoolLED’s “Sequence Runner” multiple channel excitation mode.  Users can define the order of their fluorophore capture using their pE-300ultra Control Pod, then the pE-300ultra light source can accept a single TTL output from the experiment set-up’s camera to initiate the step-through of a sequence of excitation channels.  This feature is independent of the individual channel TTL inputs on the light source.  This offers users the facility to run through a sequence of excitation channels using a camera which has only a single TTL-out.

With an expected lifetime in excess of 25,000 on hours and a comprehensive range of microscope adaptors, the pE-300ultra can be fitted to most current and older microscopes and operate for many years without aligning or replacing bulbs. The result is a safe, convenient illumination system without any additional operating costs.

 

 

There are two pE-300ultra configuration options:

Direct-fit for connecting to a microscopes – by selecting from a range of microscope adaptors  which covers all current and most older models.  A simple once only adjustment will allow optimisation to the optical path of the microscope.

Liquid Light Guidewith a fixed 3mm diameter, liquid light guide.  An optional pE-Universal Collimator can be specified in conjunction with a microscope adaptor if required.

 

The pE-300ultra offers:

  • Clean bright illumination across the spectrum – excites common fluorescent stains
  • Specify for  existing single and multi-band filter sets – no need to buy new filters
  • Instant on/off – No shutters required, no warm up or cool down
  • Simple to fit, simple to use – no alignment, a once only adjustment
  • Stable & repeatable – reliable and consistent results
  • Wide range of microscope adaptors – fits most microscopes
  • Precise intensity control in 1% steps (0-100%) – no ND filters required
  • Excellent uniformity over field of view – fixed and stable, no alignment necessary
  • Long lifetime – expected to exceed 25,000 hours of operating time
  • Removable inline excitation filter holders – no moving parts
  • Individual channel triggering via TTL in microseconds
  • Sequence Runner – sequenced excitation from a single TTL-out

 

 

 

pE-100wht

The pE-100wht offers:

CoolLED pE-100wht

  • Spectral performance matched to 100W halogen – familiar images
  • No variation in colour across intensity range – no need to colour balance
  • Replaces 100W halogen lamp housing on most current and older microscopes – quick & easy exchange
  • No unwanted UV – reduced risk of eye damage
  • Instant on/off  – no shutters required, no warm up or cool down
  • Simple to fit, simple to use – no need to align
  • Stable & repeatable – reliable and consistent results
  • Wide range of microscope adaptors – fits most microscopes
  • Precise intensity control in 1% steps (0-100%) – no ND filters required
  • Excellent uniformity over field of view – fixed and stable, no alignment necessary
  • Long lifetime – expected to exceed 50,000 hours of operating time

 

 

JNO-WICD-02

JNO-WICD-02

Filter Holder for BX50 WI

(OLYMPUS  – 32BP775)

45㎜ holder for 32㎜ filter

 

  •  45㎜ 필터용 위치에 32㎜ 필터를 사용할 수 있도록 만든  홀더
  • 여러개의 필터를 중첩하여 사용 가능함.
  • BX50-WI (Olympus)  광학 유닛 업그레이드시에 JNO-DICD-01과 같이 사용되어 지며,  32BP775 설치시에 필요한 홀더임.
45㎜ holder for 32㎜  filter
Filter holder for transmitted light (OLYMPUS BX)

 

DIC microscopy (검경법)

미분 간섭 관찰 관찰법 ( DIC )

Differential Interference Contrast Microscopy(DIC)


  • 미분간섭관찰법 발명자

Georges (Jerzy) Nomarski (January 6, 1919 – 1997)

프랑스 귀화 물리학자 (폴란드 태생)


  • 발명 배경

이 관찰법은 샘플이 두꺼운 경우에 후광에 의한 광학 노이즈가 발현되는 위상차 현미경과 다르게 후광 효과가 발현되지 않으며, 샘플에 입체감을 부여하여 투명한 샘플에 대하여 보다 세밀한 관찰을 가능하게 합니다.

이 관찰법은 살아있는 생물학적 시료 및 염색을 하지 않은 조직의 관찰에 폭넓게 사용되고 있습니다.


  • DIC Microscopy 원리 설명

본 관찰법은 편광필터 2개(편광자, 검광자)와 DIC 프리즘 2개의 추가 유닛으로 구성되어 진다.

가장 바깥쪽에 위치하는 편광 필터 2개(편광자,검광자)는 Cross Nichole 상태로 설치 되어 있어야 하며, 이는 두개의 유닛 사이에 광학적 특성의 변화가 있는 빛만을 통과시키겠다는 목적으로 이해하면 된다.

 편광자를 통과한 빛이 처음 프리즘에 통과하면 빛은 2개의 경로를 가지게 된다. 이 두 빛은 광학진동 방향이 직교하며, 매우 미소한 거리 차를 가지고 진행한다.

샘플을 통과하고 다음 프리즘을 통과하면서 빛은 다시 동일한 경로를 갖는 빛으로 합성되며, 이때 다른 경로를 통과하였기 때문에 동일한 위상을 갖지 못하는 경우가 발생한다.

  동일한 위상일 경우에는 보강간섭 그렇지 않는 경우에는 소멸간섭이 발생한다.

DIC Microscopy 용어 설명(보강)

  • Phase Shift 
    1. 조정 방법: 1/4람다 필터 또는 DIC 프리즘에 있는 회전 레버을 이용하여 조정한다.
    2. 발생 효과: 보여 지는 샘플의 음영을 바꿀수 있다.
  • 쾰러 조명
    1. 최근에 사용되는 대부분의 관찰법은 쾰러 조명 세팅을 기본으로 하고 있음.
    2. 쾰러 조명을 기반으로 다양한 관찰법이 설계되어 있음.
Bright Field Microscopy와 DIC Microscopy의 이미지 비교

별칭 : Normaski Interference Contrast Microscopy ( NIC )

JNO-ARM

Advance Realtime Monitor. Easy-to-Use, Image Enhancement, etc

1. Information

ARM is image analysis software for JNOPTIC AcquCAM cameras. This S/W is interchangeable with all WDM cameras regardless of camera brand and model and even more the most strength point is simple and easy use of length, area, angle, etc.ARM01

2. Simple measurement tools

toolbar

  • Measurement Tools: Count, Distance, Angle, Area, etc.
  • Guide Lines: Cross Line, Rectangular Lattice, Circular Grid
  • Scale Panel on Live/Image Screen
  • Available measurement on LIVE image and saved image mode

3-1. Specialization for observation of fluorescence images

Improvement Function about Fluorescence Microscopy Image. (Used function: Auto Level, Low level, Pseudo Color, Merge Image)
ARM02
 Bottom on the left is merged image without improvement of image. And the bottom on the right is merged image after improvement of image. These images are shot by JNOPTIC AcquCAM Pro/G3 camera

3-2-1 Effect of high-contrast image with simple operation (Monochrome)

Improvement Function about Microscopy Image Monochrome. (Used function: Auto Level)arm04Effective improvement of image with simple operation. This image is shot by JNOPTIC Pro/S3 camera

3-2-2 Effect of high-contrast image with simple operation (Color)

Improvement Function about Microscopy Image. (Used function: Auto Level)arm05Effective improvement of image with simple operation. These images are shot by JNOPTIC AcquCAM Pro/G3 camera

3-3-1 Live Pseudo Color (for color camera)

When you get fluorescence images using color camera, if the unwanted channel was shown because of cross talk, you could remove this channel to take advantage of function of Live Pseudo.
Improvement Function about Fluorescence Microscopy Live Camera Image. (Used function: Live Pseudo Color)
arm06
 The extraction of wanted color information from color image (Remove BR on RGB source) These images are shot by JNOPTIC AcquCAM Pro/G3 camera

3-3-2 Live Pseudo Color (for Monochrome camera)

When you get fluorescence images using monochrome camera, you can raise efficiency of acquisition for fluorescence images to add similar false color to the color to be shown on the eyepiece in real time.
Improvement Function about Fluorescence Microscopy Live Monochrome Camera Image. (Used function: Live Pseudo Color)
arm08
 Improvement of usage environment for monochrome camera to add false color on the image. These images are shot by JNOPTIC AcquCAM Pro/S3 camera

4. JNO-MHU(Option Unit)

Available measuring height with additional unit, JNO-MHU
※ JNO-MHU is sold separately as optional unit.
jno-mhu1
  jno-mhu2
 Left: Focus on top of sample (Z-axis reset), Right: Focus on bottom of sample (Z-axis height measurement)
jno-mhu3
 < Measuring condition : over 20x objective, temp 20°C >
Responding Model Measurement value unit Measurable height Error of measuring 1000㎛ Recommended measuring height
CX 41 0.2 ㎛ -9.9 ~ 29.9㎜ Below ±20㎛ Below ± 2000㎛
CKX 41 0.2 ㎛ -9.9 ~ 29.9㎜ Below ±20㎛ Below ± 2000㎛
BX – FM 0.2 ㎛ -9.9 ~ 29.9㎜ Below ±20㎛ Below ± 2000㎛
BX 51/53 0.1 ㎛ -9.9 ~ 29.9㎜ Below ±10㎛ Below ± 1000㎛
MX 51 0.1 ㎛ -9.9 ~ 29.9㎜ Below ±10㎛ Below ± 1000㎛
MX 61L/61 0.1 ㎛ -9.9 ~ 29.9㎜ Below ±10㎛ Below ± 1000㎛

5. Reporting to Excel

excel