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Citations & References (13)
Invitrogen™
Biocytin Hydrazide
Biocytin hydrazide an be used as microinjectable anterograde and transneuronal tracers that is fixable with aldehyde-based fixatives. Additionally, the primaryRead more
| Catalog Number | Quantity |
|---|---|
| B1603 also known as B-1603 | 25 mg |
Catalog number B1603
also known as B-1603
Price (MXN)
-
Quantity:
25 mg
Biocytin hydrazide an be used as microinjectable anterograde and transneuronal tracers that is fixable with aldehyde-based fixatives. Additionally, the primary aliphatic amine of this molecule can be reversibly coupled to aldehydes and ketones to form a Schiff base - which can be reduced to a stable amine derivative by sodium borohydride (NaBH4) or sodium cyanoborohydride (NaCNH3) to form new biotinylated probes. Carboxylic acids of proteins and other water-soluble biopolymers can be coupled to this molecule in aqueous solution using water-soluble carbodiimides such as EDAC (E2247).
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Label TypeBiotin & Other Haptens
Product TypeBiocytin Hydrazide
Quantity25 mg
Reagent TypeBiocytins
Shipping ConditionRoom Temperature
Unit SizeEach
Contents & Storage
Store at room temperature.
Citations & References (13)
Citations & References
Abstract
Signal propagation in Drosophila central neurons.
Journal:J Neurosci
PubMed ID:19439602
'Drosophila is an important model organism for investigating neural development, neural morphology, neurophysiology, and neural correlates of behaviors. However, almost nothing is known about how electrical signals propagate in Drosophila neurons. Here, we address these issues in antennal lobe projection neurons, one of the most well studied classes of Drosophila
Enzyme-modulated cleavage of dsDNA for supramolecular design of biosensors.
Journal:Anal Chem
PubMed ID:11721929
'Supramolecular docking and immobilization of biotinylated dsDNA onto a self-assembled monolayer of avidin have been measured using impedance spectroscopy and quartz crystal microbalance technique. The formation of the serial assembly was first achieved by linearizing circular plasmid dsDNA using BamH I endonuclease enzyme. This was followed by a bisulfite-catalyzed transamination
Selective labeling of functional groups on membrane proteins or glycoproteins using reactive biotin derivatives and 125I-streptavidin.
Journal:Biochem Biophys Res Commun
PubMed ID:3085669
'Amino groups, sulfhydryl groups or oxidation-induced aldehydes on erythrocyte membrane proteins and/or glycoproteins, were reacted with biotinyl N-hydroxysuccinimide ester (BNHS), 3-(N-maleimido-propionyl) biocytin (MPB) or biocytin hydrazide (BCHZ), respectively. The detergent-lysed biotinylated samples were subjected to SDS-polyacrylamide gel electrophoresis, and the proteins were transferred onto nitrocellulose membranes. The blot was then
Capture of peptides with N-terminal serine and threonine: a sequence-specific chemical method for Peptide mixture simplification.
Journal:Bioconjug Chem
PubMed ID:12526710
'The objective of this study was to evaluate a sequence-specific chemistry for the ability to specifically capture peptides that contain N-terminal serine or threonine residues from mixtures. The first step is the oxidation of the 1,2-amino alcohol structure -CH(NH(2))CH(OH)- of peptides containing N-terminal serine or threonine with periodate. The newly
Detection of protein carbonyls by means of biotin hydrazide-streptavidin affinity methods.
Journal:Methods Mol Biol
PubMed ID:19378083
'Oxidative posttranslational protein modifications occur as a normal process of cell biology and to a greater extent during pathogenic conditions. The detection and quantitation of protein oxidation has posed a continuing challenge to bioanalytical chemists because the products of oxidative protein damage are chemically diverse, protein oxidation generally occurs at