Search
Zitierungen und Referenzen (130)
Invitrogen™
BODIPY™ FL C5-Ceramid zu BSA komplexiert
BODIPY™ FL C5 Ceramid, das zu BSA komplexiert wurde, kann in Sphingolipid-Transport- und Stoffwechselmechanismen verwendet werden. Die Komplexierung fluoreszierender LipideWeitere Informationen
| Katalognummer | Menge |
|---|---|
| B22650 | 5 mg |
Katalognummer B22650
Preis (EUR)
678,00
Each
Menge:
5 mg
Preis (EUR)
678,00
Each
BODIPY™ FL C5 Ceramid, das zu BSA komplexiert wurde, kann in Sphingolipid-Transport- und Stoffwechselmechanismen verwendet werden. Die Komplexierung fluoreszierender Lipide mit Rinderserumalbuin (BSA) erleichtert die Zellmarkierung, da organische Lösungsmittel zur Auflösung der lipophilen Sonde nicht mehr benötigt werden. Die BSA-komplexierte Sonde kann direkt in Wasser aufgelöst werden.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
Chemischer Name oder MaterialSphingolipide
Empfohlene LagerungBei -5 bis -30 °C lagern und vor Licht schützen.
Physikalische FormFest
ProduktlinieBODIPY
Menge5 mg
Unit SizeEach
Zitierungen und Referenzen (130)
Zitierungen und Referenzen
Abstract
Centrosome localization determines neuronal polarity.
Journal:Nature
PubMed ID:16079847
'Neuronal polarization occurs shortly after mitosis. In neurons differentiating in vitro, axon formation follows the segregation of growth-promoting activities to only one of the multiple neurites that form after mitosis. It is unresolved whether such spatial restriction makes use of an intrinsic program, like during C. elegans embryo polarization, or
Time-lapse analysis and mathematical characterization elucidate novel mechanisms underlying muscle morphogenesis.
Journal:PLoS Genet
PubMed ID:18833302
'Skeletal muscle morphogenesis transforms short muscle precursor cells into long, multinucleate myotubes that anchor to tendons via the myotendinous junction (MTJ). In vertebrates, a great deal is known about muscle specification as well as how somitic cells, as a cohort, generate the early myotome. However, the cellular mechanisms that generate
Two-photon fluorescence absorption and emission spectra of dyes relevant for cell imaging.
Journal:J Microsc
PubMed ID:12423261
'Two-photon absorption and emission spectra for fluorophores relevant in cell imaging were measured using a 45 fs Ti:sapphire laser, a continuously tuneable optical parametric amplifier for the excitation range 580-1150 nm and an optical multichannel analyser. The measurements included DNA stains, fluorescent dyes coupled to antibodies as well as organelle
Use of fluorescent dyes for measurement and localization of organelles associated with Ca2+ store release in human neutrophils.
Journal:Cell Biol Int
PubMed ID:9693835
'Fura-2 and its lipid analogue, FFP-18, were used to measure changes in cytosolic free Ca2+ concentration within human neutrophils. Whereas fura-2 was employed to monitor cytosolic Ca2+ increases throughout the cytosol, FFP-18 was used to monitor Ca2+ changes only near the membrane. This latter probe was incorporated into the plasma
Changes in architecture of the Golgi complex and other subcellular organelles during myogenesis.
Journal:J Cell Biol
PubMed ID:7678420
'Myogenesis involves changes in both gene expression and cellular architecture. Little is known of the organization, in muscle in vivo, of the subcellular organelles involved in protein synthesis despite the potential importance of targeted protein synthesis for formation and maintenance of functional domains such as the neuromuscular junction. A panel