67769-47-5
Chemical Structure
Luc Yellow CH dilithium
- CAS No.: 67769-47-5
- Formula:C13H9Li2N5O9S2
- Molecular Weight:457.25
IUPAC Name: lithium 6-amino-2-(hydrazinecarboxamido)-1,3-dioxo-2,3-dihydro-1H-benzo[de]isoquinoline-5,8-disulfonate
InChIKey: RPKCZJYDUKVMGF-UHFFFAOYSA-L
SMILES: O=S(C1=C(N)C2=CC(S(=O)(O[Li])=O)=CC(C(N(NC(NN)=O)C3=O)=O)=C2C3=C1)(O[Li])=O
Biological Activity: Luc Yellow CH dilithium is a high-intensity fluorescent probe containing free hydrazyl groups. Luc Yellow CH can react with fatty aldehydes at room temperature. Luc Yellow CH serves as a biological tracer to monitor neuronal branching, regeneration, gap junction detection and characterization, and selective ablation of cells after aldehyde fixation. Luc Yellow CH displays the maximum excitation/emission of 430 nm/540 nm, respectively[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Luc Yellow CH dilithium | 99.67% | Luc Yellow CH dilithium is a high-intensity fluorescent probe containing free hydrazyl groups. Luc Yellow CH can react with fatty aldehydes at room temperature. Luc Yellow CH serves as a biological tracer to monitor neuronal branching, regeneration, gap junction detection and characterization, and selective ablation of cells after aldehyde fixation. Luc Yellow CH displays the maximum excitation/emission of 430 nm/540 nm, respectively. | ||||||||||||||||||||
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References
- [1]. Stewart WW. Functional connections between cells as revealed by dye-coupling with a highly fluorescent naphthalimide tracer. Cell. 1978 Jul;14(3):741-59. [Content Brief]
- [2]. Klein M, et al. Transport of lucifer yellow CH into plant vacuoles--evidence for direct energization of a sulphonatedsubstance and implications for the design of new molecular probes. FEBS Lett. 1997 Dec 22;420(1):86-92. [Content Brief]
