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Zitierungen und Referenzen (22)
Invitrogen™
DQ™ Green BSA - Special Packaging
DQ Green BSA ist ein fluorogenes Substrat für Proteasen. Ein starker Fluoreszenz-Löscheffekt wird beobachtet, wenn Proteine stark mit BODIPY-Farbstoffen markiertWeitere Informationen
| Katalognummer | Menge |
|---|---|
| D12050 | 5 × 1 mg |
Katalognummer D12050
Preis (EUR)
597,92
Sonderangebot
Exklusiv online
Endet: 15-Mar-2026
808,00Ersparnis 210,08 (26%)
Each
Menge:
5 × 1 mg
Preis (EUR)
597,92
Sonderangebot
Exklusiv online
Endet: 15-Mar-2026
808,00Ersparnis 210,08 (26%)
Each
DQ Green BSA ist ein fluorogenes Substrat für Proteasen. Ein starker Fluoreszenz-Löscheffekt wird beobachtet, wenn Proteine stark mit BODIPY-Farbstoffen markiert sind. Nach der Hydrolyse von DQ Green BSA zu einzelnen, farbstoffmarkierten Peptiden durch Proteasen wird diese Abschreckung erleichtert und produziert hell fluoreszierende Produkte.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
ProduktlinieDQ
Menge5 × 1 mg
VersandbedingungRaumtemperatur
SubstratProtease-Substrat
NachweisverfahrenFluoreszent
FormFest
Substrate PropertiesProtein-basiertes Substrat
Unit SizeEach
Inhalt und Lagerung
Bei -5 bis -30 °C lagern und vor Licht schützen.
Zitierungen und Referenzen (22)
Zitierungen und Referenzen
Abstract
Beclin1-binding UVRAG targets the class C Vps complex to coordinate autophagosome maturation and endocytic trafficking.
Journal:Nat Cell Biol
PubMed ID:18552835
'Autophagic and endocytic pathways are tightly regulated membrane rearrangement processes that are crucial for homeostasis, development and disease. Autophagic cargo is delivered from autophagosomes to lysosomes for degradation through a complex process that topologically resembles endosomal maturation. Here, we report that a Beclin1-binding autophagic tumour suppressor, UVRAG, interacts with the
A cytosolic calcium transient is not necessary for degranulation or oxidative burst in immune complex-stimulated neutrophils.
Journal:J Leukoc Biol
PubMed ID:9307071
'Receptor-mediated activation of neutrophils (PMN) initiates possibly interdependent events, including a rapid transient increase in [Ca2+]i, implicated as a second messenger. To investigate whether this transient is required for eventual degranulation, PMN were incubated with an intracellular Ca2+ chelator (BAPTA), then exposed to chemotactic peptide [N-formyl-methionyl-leucyl-phenylalanine (fMLP)l with or without
Maturation and trafficking of monocyte-derived dendritic cells in monkeys: implications for dendritic cell-based vaccines.
Journal:J Immunol
PubMed ID:10679086
'Human dendritic cells (DC) have polarized responses to chemokines as a function of maturation state, but the effect of maturation on DC trafficking in vivo is not known. We have addressed this question in a highly relevant rhesus macaque model. We demonstrate that immature and CD40 ligand-matured monocyte-derived DC have
A novel methodology for the investigation of intracellular proteolytic processing in intact cells.
Journal:Eur J Cell Biol
PubMed ID:9548376
'Taking advantage of the unique spectral properties of the fluorescent probe FL-Bodipy, we have developed a new methodology to study processing of exogenous proteins in intact cells. FL-Bodipy was conjugated to bovine serum albumin (BSA) at a molar ratio of 29 probe molecules to 1 albumin equivalent. The resulting conjugate
Assays to assess autophagy induction and fusion of autophagic vacuoles with a degradative compartment, using monodansylcadaverine (MDC) and DQ-BSA.
Journal:Methods Enzymol
PubMed ID:19200877
In this chapter we describe the use of monodasylcadaverine (MDC) and DQ-BSA, two practical and convenient tools to study the autophagic pathway. MDC is a lysosomotropic compound useful for the identification of autophagic vesicles by fluorescence microscopy and, in addition, to assess autophagy induction via the accumulation of MDC-labeled vacuoles.