210236-90-1
Chemical Structure
Fluorescein tyramide
- CAS No.: 210236-90-1
- Formula:C29H21NO7
- Molecular Weight:495.49
IUPAC Name: N-(4-hydroxyphenethyl)acetamide compound with 3',6'-dihydroxy-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one (1:1)
InChIKey: RIHCPYWHAYBEHO-UHFFFAOYSA-N
SMILES: O=C1OC2(C3=C(OC4=C2C=CC(O)=C4)C=C(O)C=C3)C5=C1C=CC=C5.O=C(C)NCCC6=CC=C(O)C=C6
Biological Activity: Fluorescein tyramide is a green fluorescent reagent (λabs: 494 nm; λem: 517 nm). Fluorescein tyramide is widely used for tyramide signal amplification (TSA) with a low-abundance in IHC, ICC, in situ hybridization (FISH) and flow cytometry (FCM) applications[1][2].
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Fluorescein tyramide | 95.98% | Fluorescein tyramide is a green fluorescent reagent (λabs: 494 nm; λem: 517 nm). Fluorescein tyramide is widely used for tyramide signal amplification (TSA) with a low-abundance in IHC, ICC, in situ hybridization (FISH) and flow cytometry (FCM) applications. | ||||||||||||||||||||
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- [1]. A H Hopman, et al. Rapid synthesis of biotin-, digoxigenin-, trinitrophenyl-, and fluorochrome-labeled tyramides and their application for In situ hybridization using CARD amplification. J Histochem Cytochem. 1998 Jun;46(6):771-7. [Content Brief]
- [2]. R P van Gijlswijk, et al. Fluorochrome-labeled tyramides: use in immunocytochemistry and fluorescence in situ hybridization. J Histochem Cytochem. 1997 Mar;45(3):375-82. [Content Brief]
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