Biotin-X, SE (6-((Biotinoyl)Amino)Hexanoic Acid, Succinimidyl Ester (Biotinamidocaproate, N-Hydroxysuccinimidyl Ester))
Biotin-X, SE (6-((Biotinoyl)Amino)Hexanoic Acid, Succinimidyl Ester (Biotinamidocaproate, <i>N</i>-Hydroxysuccinimidyl Ester))
Invitrogen™

Biotin-X, SE (6-((Biotinoyl)Amino)Hexanoic Acid, Succinimidyl Ester (Biotinamidocaproate, N-Hydroxysuccinimidyl Ester))

Das aminreaktive Biotin-X, SE kann verwendet werden, um dieses wichtige Hapten an bestimmte Biomoleküle zum nachfolgenden Nachweis mit Streptavidin, AvidinWeitere Informationen
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KatalognummerMenge
B1582
auch als B-1582 bezeichnet
100 mg
Katalognummer B1582
auch als B-1582 bezeichnet
Preis (EUR)
418,00
Each
Zum Warenkorb hinzufügen
Menge:
100 mg
Preis (EUR)
418,00
Each
Zum Warenkorb hinzufügen
Das aminreaktive Biotin-X, SE kann verwendet werden, um dieses wichtige Hapten an bestimmte Biomoleküle zum nachfolgenden Nachweis mit Streptavidin, Avidin oder NeutrAvidin™ Biotin-bindenden Proteinen anzuhängen.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
Chemische ReaktivitätAmin
Marker oder FarbstoffBiotin-X
ProdukttypBiotin-XX, SE
Menge100 mg
Reaktiver TeilAktiv-Ester, Succinimidylester
VersandbedingungRaumtemperatur
MarkertypBiotin und andere Haptene
Unit SizeEach
Inhalt und Lagerung
Im Gefrierschrank lagern (-5 bis -30 °C).

Zitierungen und Referenzen (87)

Zitierungen und Referenzen
Abstract
Peptide biotinylation with amine-reactive esters: differential side chain reactivity.
Authors:Miller BT, Collins TJ, Rogers ME, Kurosky A
Journal:Peptides
PubMed ID:9437720
N-hydroxysuccinimide (NHS) esters of biotin are reported to react specifically with amino groups of peptides and proteins. However, we have found that these reagents can readily acylate other functional groups in specific peptide sequences under relatively mild conditions. We have extended our inquiry of sequence-dependent acylation by evaluating the reactivity ... More
Enumeration of antigen-specific IgE responses at the single-cell level by an ELISA plaque assay.
Authors:Chen SS
Journal:J Immunol Methods
PubMed ID:1703186
In vitro elicitation and enumeration of antigen-specific IgE-secreting cells in antigen-primed murine lymphocyte cultures can be reproducibly and accurately quantitated. Rat anti-mouse IgE monoclonal antibodies (Mab anti-epsilon) were developed. Antigen-specific IgE-secreting cells can be detected on antigen or MAb anti-epsilon coated nitrocellulose discs pasted to 24-well culture plates. This IgE ... More
A novel fluorescent toxin to detect and investigate Kv1.3 channel up-regulation in chronically activated T lymphocytes.
Authors:Beeton C, Wulff H, Singh S, Botsko S, Crossley G, Gutman GA, Cahalan MD, Pennington M, Chandy KG
Journal:J Biol Chem
PubMed ID:12511563
T lymphocytes with unusually high expression of the voltage-gated Kv1.3 channel (Kv1.3(high) cells) have been implicated in the pathogenesis of experimental autoimmune encephalomyelitis, an animal model for multiple sclerosis. We have developed a fluoresceinated analog of ShK (ShK-F6CA), the most potent known inhibitor of Kv1.3, for detection of Kv1.3(high) cells ... More
Biochemical analysis of connexin43 intracellular transport, phosphorylation, and assembly into gap junctional plaques.
Authors:Musil LS, Goodenough DA
Journal:J Cell Biol
PubMed ID:1659577
'We previously demonstrated that the gap junction protein connexin43 is translated as a 42-kD protein (connexin43-NP) that is efficiently phosphorylated to a 46,000-Mr species (connexin43-P2) in gap junctional communication-competent, but not in communication-deficient, cells. In this study, we used a combination of metabolic radiolabeling and immunoprecipitation to investigate the assembly ... More
Localized suppression of RhoA activity by Tyr31/118-phosphorylated paxillin in cell adhesion and migration.
Authors:Tsubouchi A, Sakakura J, Yagi R, Mazaki Y, Schaefer E, Yano H, Sabe H
Journal:J Cell Biol
PubMed ID:12446743
'RhoA activity is transiently inhibited at the initial phase of integrin engagement, when Cdc42- and/or Rac1-mediated membrane spreading and ruffling predominantly occur. Paxillin, an integrin-assembly protein, has four major tyrosine phosphorylation sites, and the phosphorylation of Tyr31 and Tyr118 correlates with cell adhesion and migration. We found that mutation of ... More