1. Others Metabolic Enzyme/Protease
  2. Fluorescent Dye γ-Glutamyl Transferase (GGT)
  3. C-HBrO-GGT

C-HBrO-GGT is a sequence-activated two-photon fluorescent probe. C-HBrO-GGT exhibits sequential fluorescence activation properties: it generates fluorescence in response to hypobromous acid only after being hydrolytically activated by γ-glutamyl transpeptidase. C-HBrO-GGT enables verification of the voltage-gated chloride channel (CLC-1)-HBrO-catalase (CAT)-GGT signaling pathway at the cellular level. C-HBrO-GGT can serve as a tool to indicate the precise location of mature atherosclerotic plaques and provide early warning of plaque formation. C-HBrO-GGT is applicable to relevant research on atherosclerosis.

For research use only. We do not sell to patients.

C-HBrO-GGT

C-HBrO-GGT Chemical Structure

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Description

C-HBrO-GGT is a sequence-activated two-photon fluorescent probe. C-HBrO-GGT exhibits sequential fluorescence activation properties: it generates fluorescence in response to hypobromous acid only after being hydrolytically activated by γ-glutamyl transpeptidase. C-HBrO-GGT enables verification of the voltage-gated chloride channel (CLC-1)-HBrO-catalase (CAT)-GGT signaling pathway at the cellular level. C-HBrO-GGT can serve as a tool to indicate the precise location of mature atherosclerotic plaques and provide early warning of plaque formation. C-HBrO-GGT is applicable to relevant research on atherosclerosis[1].

In Vitro

C-HBrO-GGT reacts sequentially with GGT and HBrO in order, as confirmed by HPLC peak shifts corresponding to the formation of intermediate and final reaction products[1].
C-HBrO-GGT (10 μM; 30 min) exhibits high sensitivity and good affinity for GGT in vitro, enabling quantitative detection of GGT activity with a detection limit of 0.076 U/L[1].
GGT-activated C-HBrO-GGT (10 μM; overnight GGT activation) exhibits high sensitivity for HBrO in vitro, enabling quantitative detection of HBrO concentrations with a linear response across 0-12 μM[1].
C-HBrO-GGT shows high selectivity for GGT and HBrO under physiological conditions, with optimal response to GGT at pH 7-9[1].
C-HBrO-GGT (10 μM; 30 min) detects significantly elevated GGT activity and HBrO concentrations in ox-LDL-induced RAW 264.7 foam cells compared to untreated RAW 264.7 cells[1].
C-HBrO-GGT uses TP fluorescence to detect elevated GGT activity and HBrO concentrations in NaBr-induced RAW 264.7 and SMMC-7721 cells, and confirms that increased HBrO indirectly elevates GGT activity[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

C-HBrO-GGT (i.v.) enables in situ, selective two-channel fluorescence detection of elevated GGT activity and HBrO levels at atherosclerotic plaques in ApoE-/-/HF mice, with fluorescence intensities significantly higher than those in control C57BL/6 J mice[1].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Molecular Weight

480.46

Formula

C22H19F3N2O5S

SMILES

CSC1=CC=CC=C1C2=C3OC(C=C(C3=CC=C2NC(CCC(C(O)=O)N)=O)C(F)(F)F)=O

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Room temperature in continental US; may vary elsewhere.

Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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Help & FAQs
  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
C-HBrO-GGT
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HY-D3170
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