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Zitierungen und Referenzen (7)
Invitrogen™
InSpeck™ Green (505/515) Microscope Image Intensity Calibration Kit, 6 μm
6,0 µm InSpeck Mikrokugeln in diesem Kit haben einen ähnlichen Durchmesser wie viele gefärbte Zellen und bieten Intensitätsreferenzen für dieWeitere Informationen
| Katalognummer | Menge |
|---|---|
| I14785 auch als I-14785 bezeichnet | 1 kit |
Katalognummer I14785
auch als I-14785 bezeichnet
Preis (EUR)
406,00
Each
-
Menge:
1 kit
Preis (EUR)
406,00
Each
6,0 µm InSpeck Mikrokugeln in diesem Kit haben einen ähnlichen Durchmesser wie viele gefärbte Zellen und bieten Intensitätsreferenzen für die Fluoreszenzmikroskopie zur Erstellung von Kalibrierungskennlinien und Bewertung der Geräteleistung. Wässrige Suspensionen von Mikrokugeln lassen sich zur Kalibrierung von Fluoreszenzintensitäten direkt auf die Probe oder gesondert im angrenzenden Well oder auf einem anderen Objektträger aufbringen.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
KalibrierungsartMikroskop-Bildintensitätskalibrierung
FarbeGrün
Durchmesser (metrisch)6 μm
FormatSuspensions-Beads
Menge1 kit
VersandbedingungRaumtemperatur
ProduktlinieInSpeck™
TypMikroskop-Bildintensitätskalibrierungskit
Unit SizeEach
Inhalt und Lagerung
Im Kühlschrank (2–8 °C) aufbewahren und vor Licht schützen.
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Abbildungen
Flow cytometric analysis of the beads in the 6 µm InSpeck™ Green Microscope Image Intensity Calibration Kit.
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Zertifikate
Nach Chargennummer oder Teil-Chargennummer suchen
Chargen-Nr.Certificate TypeDateCatalog Number(s)
3038111Certificate of Analysis17. Dez. 2024I14785
2644202Certificate of Analysis20. Juni 2023I14785
2407893Certificate of Analysis09. Okt. 2021I14785
2407893Certificate of Analysis21. Sept. 2021I14785
108017Certificate of Analysis27. Juli 2017I14785
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SDBProduct Information
Handbuch Molecular Probes®
Zitierungen und Referenzen (7)
Search citations by name, author, journal title or abstract text
Zitierungen und Referenzen
Abstract
Immunohistochemical localization of inhibin/activin alpha, betaA and betaB subunits and follistatin in bovine oocytes during in vitro maturation and fertilization.
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
Quantitative fluorescence imaging analysis for cancer biomarker discovery: application to beta-catenin in archived prostate specimens.
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
Quantization of widefield fluorescence images using structured illumination and image analysis software.
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
Macaque trophoblast migration is regulated by RANTES.
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
Highly Sensitive Shack-Hartmann Wavefront Sensor: Application to Non-Transparent Tissue Mimic Imaging with Adaptive Light-Sheet Fluorescence Microscopy.
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
7 total citations