Der zellpermeable, fixierbare und polare Tracer Cascade Blue™ Hydrazid kann zur Untersuchung der Zell-Zell- und Zell-Liposomen-Fusion sowie der Membrandurchlässigkeit undWeitere Informationen
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Katalognummer
Menge
C687
10 mg
Katalognummer C687
Preis (EUR)
486,00
Each
Zum Warenkorb hinzufügen
Menge:
10 mg
Preis (EUR)
486,00
Each
Zum Warenkorb hinzufügen
Der zellpermeable, fixierbare und polare Tracer Cascade Blue™ Hydrazid kann zur Untersuchung der Zell-Zell- und Zell-Liposomen-Fusion sowie der Membrandurchlässigkeit und zum Transport durch Lückenverbindungen oder die Zellaufnahme während der Pinocytose verwendet werden. Dieser wasserlösliche Tracer kann mittels der Whole-Cell-Patch-Clamp-Technik, Iontophorese, osmotischer Lyse von pinozytischen Vesikeln oder vergleichbare Methoden in die Zellen eingebracht werden. Darüber hinaus können Carbonsäuren von Proteinen und anderen wasserlöslichen Biopolymeren in wässriger Lösung mit wasserlöslichen Carbodiimiden wie EDAC (E2247) an dieses Molekül gekoppelt werden.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
Chemische ReaktivitätCarbonsäure, Keton, Aldehyd
Emission412 nm
Anregung399 nm
Marker oder FarbstoffCascade Blue™
Molekulargewicht596.44 G/MOL
ProdukttypHydrazid
Menge10 mg
Reaktiver TeilAmin, Hydrazid
VersandbedingungRaumtemperatur
MarkertypKlassische Farbstoffe
ProduktlinieCASCADE BLUE
Unit SizeEach
Inhalt und Lagerung
Lagerung bei Raumtemperatur und vor Licht geschützt
Häufig gestellte Fragen (FAQ)
What is the recommended concentration for preparation of Cascade Blue hydrazide, Trisodium Salt (Cat. No. C687) stock solution?
We recommend preparing a 1% w/v stock solution in sterile water. Please note that the dye can aggregate in solution over time.
Zitierungen und Referenzen (24)
Zitierungen und Referenzen
Abstract
Parathyroid hormone controls the size of the intracellular Ca(2+) stores available to receptors linked to inositol trisphosphate formation.
Authors:Short AD, Taylor CW
Journal:J Biol Chem
PubMed ID:10636879
'In HEK 293 cells stably expressing type 1 parathyroid (PTH) receptors, PTH stimulated release of intracellular Ca(2+) stores in only 27% of cells, whereas 96% of cells responded to carbachol. However, in almost all cells PTH potentiated the response to carbachol by about 3-fold. Responses to carbachol did not desensitize, ... More
Neuropeptides exert direct effects on rat thymic epithelial cells in culture.
Authors:Head GM, Mentlein R, von Patay B, Downing JE, Kendall MD
Journal:Dev Immunol
PubMed ID:9716910
'To determine if major thymic neuropeptides and neurotransmitters can directly influence the functional activity of cultured rat thymic epithelium, neuropeptides and neurotransmitters were applied, and intercellular communication, proliferation, and thymulin secretion assessed. After injections of a mixture of lucifer yellow dextran (too large to pass gap junctions) and cascade blue ... More
Oligosaccharide organization of the beta-subunits of pig kidney Na+/K+-ATPase.
Authors:Amler E, Staffolani R, Baranska J, Obsil T, Urbanová P, Bertoli E, Mazzanti L
Journal:Physiol Res
PubMed ID:9730046
'The distance between the beta-subunits of Na+/K+-ATPase isolated from pig dark red kidney medulla was determined by Förster energy transfer. First, oligosaccharides of the beta-subunit were shown to be labelled with three fluorophores: Lucifer yellow (LY), Lissamine rhodamine B sulfonyl hydrazine (LRSH) and Cascade blue (CB). Further, LY and LRSH ... More
Site-directed conjugation of nonpeptide groups to peptides and proteins via periodate oxidation of a 2-amino alcohol. Application to modification at N-terminal serine.
Authors:Geoghegan KF, Stroh JG
Journal:Bioconjug Chem
PubMed ID:1325188
'The 2-amino alcohol structure -CH(NH2)CH(OH)- exists in proteins and peptides in N-terminal Ser or Thr and in hydroxylysine. Its very rapid oxidation by periodate at pH 7 generates an aldehyde in the peptide and is the first step in a method for site-directed labeling with biotin or a fluorescent reporter. ... More
Functional analysis of amino acid sequences in connexin43 involved in intercellular communication through gap junctions.
Authors:Becker DL, Evans WH, Green CR, Warner A
Journal:J Cell Sci
PubMed ID:7615666
'Gap junctions allow direct communication between cells without recourse to the extracellular space and have been widely implicated as important mediators of cell-cell signalling. They are constructed from the connexin proteins, which form a large family, and individual connexins show complex spatial and temporal variations in their expression patterns. Understanding ... More