also known as Alexa Fluor® 546 tyramide
For research use only!
Shipping: shipped on gel packs
Storage Conditions: store at -20 °C
Shelf Life: 12 months after date of delivery
Molecular Formula: C60H83Cl3N6O12S3
Molecular Weight: 1282.88 g/mol
Exact Mass: 1280.43 g/mol
Purity: ≥ 95 % (HPLC)
Spectroscopic Properties: λexc 561 nm, λem 572 nm, ε 112.0 L mmol-1 cm-1 (Tris-HCl pH 7.5)
Tyramide Signal Amplification (TSA) is a peroxidase-based signal amplification system that is compatible with all in situ hybridization (ISH), immunocytochemical (ICC) and immunohistochemistry (IHC) detection schemes involving horseradish peroxidase (HRP)-coupled detection reagents. An up to 100-fold increased assay sensitivity compared to conventional ISH, ICC and IHC methods allows the detection of low-abundance targets (e.g mRNA) while reducing primary & secondary detection reagents as well as hybridization probe concentration. The usage of poly-HRP-coupled detection reagents further increases assay sensitivity.
Principle of TSA labeling :
Hybridization probes are detected by (poly)-HRP-coupled detection reagents. TSA labeling is based on the ability of (poly)-HRP to activate multiple labeled tyramide substrates in the presence of low concentrations of hydrogen peroxide. The resulting highly reactive radicals subsequently bind to tyrosine residues at or near the HRP thereby generating high density tyramide labeling. AF546 (also known as Alexa Fluor® 546) tyramide can be detected with the standard TRITC filter set.
Preparation of 200x AF546 tyramide stock solution:
Add 100 μl DMSO, vortex and spin-down briefly. Store at 2-8°C (dark) for up to 6 months (sealed vial, desiccated).
Preparation of 1x AF546 tyramide working solution:
Working solution can not be stored and should immediately be prepared before usage. Dilute 1:200 in a buffer compatible with your downstream protocol (e.g. Tris-HCl buffer, pH 7.4) containing 0.003% H2O2, vortex and spin-down briefly. 100 μl working solution is sufficient for one 18-mm × 18-mm slide.
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