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Citations & References (26)
Invitrogen™
Alpha-Bungarotoxin Conjugates
Thermo Fisher Scientific offers a broad selection of Invitrogen alpha-bungarotoxin conjugates, including Alexa Fluor and Alexa Fluor Plus conjugates.
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| Catalog Number | Label or Dye |
|---|---|
| B13423 | Alexa Fluor™ 594 |
| B56130 | Alexa Fluor™ Plus 405 |
| B13422 | Alexa Fluor™ 488 |
| B35451 | Alexa Fluor™ 555 |
| B35450 | Alexa Fluor™ 647 |
| B1196 | Biotin-XX |
| T1175 | Tetramethylrhodamine |
| B1601 | Unlabeled |
Catalog number B13423
Price (EUR)
747,40
Special offer
Online exclusive
Ends: 15-Mar-2026
1.010,00Save 262,60 (26%)
Each
Label or Dye:
Alexa Fluor™ 594
Price (EUR)
747,40
Special offer
Online exclusive
Ends: 15-Mar-2026
1.010,00Save 262,60 (26%)
Each
Thermo Fisher Scientific offers a broad selection of Invitrogen alpha-bungarotoxin conjugates, including Alexa Fluor and Alexa Fluor Plus conjugates. Alpha-bungarotoxin, a 74-amino acid peptide extracted from Bungarus multicinctus venom, binds with high affinity to the alpha subunit of the nicotinic acetylcholine receptor (AChR) of neuromuscular junctions.
Our bright and photostable Alexa Fluor 555 alpha-bungarotoxin is a superior choice of probe for visualizing this receptor. Fluorescent alpha-bungarotoxin conjugates can be used to facilitate identification of nicotinic AChRs and localization of neuromuscular junctions. Conjugated alpha-bungarotoxin has been used in variety of applications, including immunofluorescence (IF), immunohistochemistry (IHC), and flow cytometry (FC).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Label or DyeAlexa Fluor™ 594
Product TypeConjugate
Protein SubtypeOther Proteins
Quantity500 μg
Shipping ConditionRoom Temperature
Excitation/Emission590/617 nm
Product LineAlexa Fluor
Unit SizeEach
Contents & Storage
Store in freezer (–5° to –30°C) and protect from light.
Citations & References (26)
Citations & References
Abstract
Specification of motoneurons from human embryonic stem cells.
Journal:Nat Biotechnol
PubMed ID:15685164
'An understanding of how mammalian stem cells produce specific neuronal subtypes remains elusive. Here we show that human embryonic stem cells generated early neuroectodermal cells, which organized into rosettes and expressed Pax6 but not Sox1, and then late neuroectodermal cells, which formed neural tube-like structures and expressed both Pax6 and
Local induction of acetylcholine receptor clustering in myotube cultures using microfluidic application of agrin.
Journal:Biophys J
PubMed ID:16387765
'During neuromuscular synaptogenesis, the exchange of spatially localized signals between nerve and muscle initiates the coordinated focal accumulation of the acetylcholine (ACh) release machinery and the ACh receptors (AChRs). One of the key first steps is the release of the proteoglycan agrin focalized at the axon tip, which induces the
Absence of acetylcholinesterase at the neuromuscular junctions of perlecan-null mice.
Journal:Nat Neurosci
PubMed ID:11802174
'The collagen-tailed form of acetylcholinesterase (AChE) is concentrated at the vertebrate neuromuscular junction (NMJ), where it is responsible for rapidly terminating neurotransmission. This unique oligomeric form of AChE, consisting of three tetramers covalently attached to a collagen-like tail, is more highly expressed in innervated regions of skeletal muscle fibers, where
Ex vivo imaging of motor axon dynamics in murine triangularis sterni explants.
Journal:Nat Protoc
PubMed ID:18833201
'We provide a protocol that describes an explant system that allows the dynamics of motor axons to be imaged. This method is based on nerve-muscle explants prepared from the triangularis sterni muscle of mice, a thin muscle that covers the inside of the thorax. These explants, which can be maintained
alpha-Actinin interacts with rapsyn in agrin-stimulated AChR clustering.
Journal:Mol Brain
PubMed ID:19055765
: AChR is concentrated at the postjunctional membrane at the neuromuscular junction. However, the underlying mechanism is unclear. We show that alpha-actinin, a protein known to cross-link F-actin, interacts with rapsyn, a scaffold protein essential for neuromuscular junction formation. alpha-Actinin, rapsyn, and surface AChR form a ternary complex. Moreover, the