InSpeck™ Green (505/515) Microscope Image Intensity Calibration Kit, 6 μm
Product Image
Invitrogen™

InSpeck™ Green (505/515) Microscope Image Intensity Calibration Kit, 6 μm

The 6.0 μm InSpeck microspheres in this kit have diameters close to those of many stained cells, providing fluorescence microscopists자세히 알아보기
Have Questions?
카탈로그 번호수량
I14785
I-14785으로도 사용됨
1 kit
카탈로그 번호 I14785
I-14785으로도 사용됨
제품 가격(KRW)
533,000
キャンペーン価格
Ends: 31-Dec-2025
626,000
할인액 93,000 (15%)
Each
카트에 추가하기
수량:
1 kit
제품 가격(KRW)
533,000
キャンペーン価格
Ends: 31-Dec-2025
626,000
할인액 93,000 (15%)
Each
카트에 추가하기
The 6.0 μm InSpeck microspheres in this kit have diameters close to those of many stained cells, providing fluorescence microscopists with intensity references for generating calibration curves and evaluating instrument performance. The aqueous suspension of microspheres can be directly applied to the sample for calibrating fluorescence intensities, or they can be mounted separately in an adjacent well or on another slide.
For Research Use Only. Not for use in diagnostic procedures.
사양
보정 유형Microscope Image Intensity Calibration
색상Green
직경(미터법)6 μm
형식Suspension Beads
수량1 kit
배송 조건Room Temperature
제품라인InSpeck
유형Microscope Image Intensity Calibration Kit
Unit SizeEach
구성 및 보관
Store in refrigerator 2°C to 8°C and protect from light.

인용 및 참조 문헌 (7)

인용 및 참조 문헌
Abstract
Immunohistochemical localization of inhibin/activin alpha, betaA and betaB subunits and follistatin in bovine oocytes during in vitro maturation and fertilization.
Authors:Silva CC, Groome NP, Knight PG
Journal:Reproduction
PubMed ID:12622694
'The aim of this study was to evaluate the distribution of inhibin/activin alpha, beta(A) and beta(B) subunits and follistatin in immature oocytes and in matured oocytes before and after IVF. Denuded oocytes were submitted to a whole-mount immunofluorescence procedure. Specimens were imaged and fluorescent intensities quantified by scanning laser confocal ... More
Quantitative fluorescence imaging analysis for cancer biomarker discovery: application to beta-catenin in archived prostate specimens.
Authors:Huang D, Casale GP, Tian J, Wehbi NK, Abrahams NA, Kaleem Z, Smith LM, Johansson SL, Elkahwaji JE, Hemstreet GP,
Journal:Cancer Epidemiol Biomarkers Prev
PubMed ID:17623804
The surprising disparity between the number of protein-encoding genes ( approximately 30,000) in the human genome and the number of proteins ( approximately 300,000) in the human proteome has inspired the development of translational proteomics aimed at protein expression profiling of disease states. Translational proteomics, which offers the promise of ... More
Quantization of widefield fluorescence images using structured illumination and image analysis software.
Authors:Barlow AL, Guerin CJ
Journal:Microsc Res Tech
PubMed ID:17131356
It is difficult to obtain precise quantitative measurements from fluorescent images captured from widefield microscopes. We wished to ascertain if reliable quantitative measurements of both biological and nonbiological specimens were possible using a widefield microscope equipped with a structured illumination system and image analysis software. In a nonbiological specimen, images ... More
Macaque trophoblast migration is regulated by RANTES.
Authors:Thirkill TL, Lowe K, Vedagiri H, Blankenship TN, Barakat AI, Douglas GC
Journal:Exp Cell Res
PubMed ID:15817160
In human and non-human primates, migratory trophoblasts penetrate the uterine epithelium, invade the endometrium, enter the uterine vasculature, and migrate within the arteries. The mechanisms that regulate this directional migration are unknown. We have used early gestation macaque trophoblasts to test the hypothesis that trophoblast migration is regulated by the ... More
Highly Sensitive Shack-Hartmann Wavefront Sensor: Application to Non-Transparent Tissue Mimic Imaging with Adaptive Light-Sheet Fluorescence Microscopy.
Authors:Morgado Brajones J, Clouvel G, Dovillaire G, Levecq X, Lorenzo C
Journal:Methods Protoc
PubMed ID:31336779
'High-quality in-depth imaging of three-dimensional samples remains a major challenge in modern microscopy. Selective plane illumination microscopy (SPIM) is a widely used technique that enables imaging of living tissues with subcellular resolution. However, scattering, absorption, and optical aberrations limit the depth at which useful imaging can be done. Adaptive optics ... More