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Invitrogen™
Alpha-Bungarotoxin Conjugates
Thermo Fisher Scientific ofrece una amplia selección de conjugados de alfa-bungarotoxina de Invitrogen, incluidos conjugados Alexa Flour y Alexa Flour Plus.
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| Número de catálogo | Etiqueta o tinte |
|---|---|
| B35451 | Alexa Fluor™ 555 |
| B56130 | Alexa Fluor™ Plus 405 |
| B13422 | Alexa Fluor™ 488 |
| B13423 | Alexa Fluor™ 594 |
| B35450 | Alexa Fluor™ 647 |
| B1196 | Biotin-XX |
| T1175 | Tetrametilrodamina |
| B1601 | Sin marcar |
Número de catálogo B35451
Precio (EUR)
954,00
Each
-
Etiqueta o tinte:
Alexa Fluor™ 555
Precio (EUR)
954,00
Each
Thermo Fisher Scientific ofrece una amplia selección de conjugados de alfa-bungarotoxina de Invitrogen, incluidos conjugados Alexa Flour y Alexa Flour Plus. El alfa-bungarotoxina, un aminoácido péptido de 74 aminoácidos extraído del veneno de Bungarus multicinctus, se une con alta afinidad a la subunidad A del receptor nicotínico de acetilcolina (AChR) de las uniones neuromusculares.
Thermo Fisher Scientific ofrece una amplia selección de conjugados de alfa-bungarotoxina de Invitrogen, incluidos conjugados Alexa Flour y Alexa Flour Plus. El alfa-bungarotoxina, un aminoácido péptido de 74 aminoácidos extraído del veneno de Bungarus multicinctus, se une con alta afinidad a la subunidad A del receptor nicotínico de acetilcolina (AChR) de las uniones neuromusculares. Nuestra brillante y fotoestable Alexa Fluor 555 alfa-bungarotoxina es una opción superior de sonda para visualizar este receptor.
Los conjugados fluorescentes de alfa-bungarotoxina se pueden utilizar para facilitar la identificación de AChRs nicotínicos y la localización de uniones neuromusculares. La alfa-bungarotoxina conjugada se ha utilizado en diversas aplicaciones, como la inmunofluorescencia (IF), la inmunohistoquímica (IHC) y la citometría de flujo (FC).
Los conjugados fluorescentes de alfa-bungarotoxina se pueden utilizar para facilitar la identificación de AChRs nicotínicos y la localización de uniones neuromusculares. La alfa-bungarotoxina conjugada se ha utilizado en diversas aplicaciones, como la inmunofluorescencia (IF), la inmunohistoquímica (IHC) y la citometría de flujo (FC).
For Research Use Only. Not for use in diagnostic procedures.
Especificaciones
Etiqueta o tinteAlexa Fluor™ 555
Tipo de productoConjugado
Subtipo de proteínaOtras proteínas
Cantidad500 μg
Condiciones de envíoTemperatura ambiente
Excitation/Emission555/565 nm
Línea de productosAlexa Fluor™
Unit SizeEach
Contenido y almacenamiento
Almacenar en el congelador (de –5 °C a –30 °C) y proteger de la luz.
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Certificados
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N.º de loteCertificate TypeDateCatalog Number(s)
3153014Certificate of Analysis29 jun 2025B13422
3213307Certificate of Analysis21 may 2025B56130
3147103Certificate of Analysis18 may 2025B1601
3110666Certificate of Analysis04 abr 2025B13423
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SDSCitations & References (353)
Search citations by name, author, journal title or abstract text
Citations & References
Abstract
Acetylcholine receptor aggregation at nerve-muscle contacts in mammalian cultures: induction by ventral spinal cord neurons is specific to axons.
Journal:J Neurosci
PubMed ID:7472493
We used a novel mammalian coculture system to study ACh receptor (AChR) redistribution and synaptic structure at nerve-muscle contacts. Ventral spinal cord (VSC) neurons were plated on cultures containing extensive myotubes but few fibroblasts. Neurite-induced redistribution of AChRs occurred within 6 hr after plating neurons and was maximal between 36-48
Signaling by insulin-like growth factors in paralyzed skeletal muscle: rapid induction of IGF1 expression in muscle fibers and prevention of interstitial cell proliferation by IGF-BP5 and IGF-BP4.
Journal:J Neurosci
PubMed ID:7514217
'In the absence of muscle activity, muscle fibers, muscle interstitial cells, and intramuscular nerves display characteristic reactions presumably aimed at restoring a functioning neuromuscular system and avoiding degenerative events. In partially denervated muscle these include proliferation of interstitial cells, followed by nerve sprouting. The same reactions can be induced in
Identification of nicotinic acetylcholine receptor recycling and its role in maintaining receptor density at the neuromuscular junction in vivo.
Journal:J Neurosci
PubMed ID:16251443
'In the CNS, receptor recycling is critical for synaptic plasticity; however, the recycling of receptors has never been observed at peripheral synapses. Using a novel imaging technique, we show here that nicotinic acetylcholine receptors (AChRs) recycle into the postsynaptic membrane of the neuromuscular junction. By sequentially labeling AChRs with biotin-bungarotoxin
Genetic evidence that relative synaptic efficacy biases the outcome of synaptic competition.
Journal:Nature
PubMed ID:12879071
'Synaptic activity drives synaptic rearrangement in the vertebrate nervous system; indeed, this appears to be a main way in which experience shapes neural connectivity. One rearrangement that occurs in many parts of the nervous system during early postnatal life is a competitive process called ''synapse elimination''. At the neuromuscular junction,
Precise localization of alpha7 nicotinic acetylcholine receptors on glutamatergic axon terminals in the rat ventral tegmental area.
Journal:J Neurosci
PubMed ID:15601930
'Alpha7 neuronal nicotinic acetylcholine receptors (nAChRs) constitute one of the predominant nAChR subtypes in the mammalian brain. Within the ventral tegmental area (VTA), nicotine application, paired with postsynaptic stimulation, contributes to a form of long-term potentiation, an effect attributed to presynaptic alpha7 nAChRs on glutamatergic afferents (Mansvelder and McGehee, 2000).
353 total citations