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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
169 Results for "
quenched
" in MedChemExpress (MCE) Product Catalog:
Products (169)
169 Results for "quenched" in MCE Product Catalog:
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18 Cited Publications
Synonyms: PGSK diacetate (5/6-mixture)
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Phen green SK (PGSK) diacetate (PGSK diacetate (5/6-mixture)) is a metal ion-sensitive fluorescent probe that can penetrate cell membranes. Phen green SK (PGSK) diacetate can react with a variety of metal ions, including Fe 2+, Cd 2+, Co 2+, Ni 2+, Zn 2+, etc. Phen green SK (PGSK) diacetate chelates Fe 2+, resulting in fluorescence quenching, which can be restored when a membrane-permeable chelator is added, thereby reflecting the changes in the intracellular chelatable iron pool. The excitation/emission maxima of Phen green SK diacetate are 507/532 nm, respectively .
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3 Cited Publications
Cat. No.: HY-P4931
CAS No.: 720710-69-0
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9-Amino-6-chloro-2-methoxyacridine (ACMA) is an acridine derivative and Fluorescent probe. 9-Amino-6-chloro-2-methoxyacridine inhibits viral replication, inhibits DNA synthesis and protein metabolism through cell cycle arrest, and induces lipid metabolism regulation, genotoxicity, mutagenicity, and cytotoxicity through DNA strand breaks. 9-Amino-6-chloro-2-methoxyacridine partially intercalates into DNA, forming three distinct complexes, stabilizes the DNA helix, and quenches fluorescence upon intercalation through electron transfer with guanine. 9-Amino-6-chloro-2-methoxyacridine monitors the generation and collapse of the proton motive force, H + pumping by F1F0-ATP synthase, and the collapse of pH gradients in inverted membrane vesicles. 9-Amino-6-chloro-2-methoxyacridine shows potent anti-BVDV activity. 9-Amino-6-chloro-2-methoxyacridine can be used for research on bovine viral diarrhea virus infection, leishmaniasis, and MRSA infection .
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2 Cited Publications
Cat. No.: HY-P2536
CAS No.: 305336-82-7
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2 Cited Publications
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BHQ-1 NHS is a quencher and fluorescent dye. The NHS group activates the carboxyl group on the BHQ-1 molecule, enabling it to react with amino groups (primarily primary amines) on target biomolecules to form stable amide bonds, thereby labeling the biomacromolecules with BHQ-1 .
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2 Cited Publications
Cat. No.: HY-KD1006
MCE offers a variety of multiplex fluorescence detection kits, featuring high quenching resistance, low cross-contamination, and strong stability. The five-color multiplex fluorescence staining kit can stain four indicators. (MCE offers six VF series dyes: VF 480, VF 520, VF 570, VF 620, VF 690, and VF 780; you can flexibly select according to your actual needs.)
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6-TAMRA (6-Carboxytetramethylrhodamine) is a fluorescent dye. 6-TAMRA is often used in combination with 6-FAM (HY-66021) as an acceptor or fluorescence quencher for fluorescence resonance energy transfer (FRET) in biochemical studies such as potassium ion detection and ribonuclease activity assays .
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1 Cited Publications
Cat. No.: HY-W127703
CAS No.: 65603-19-2
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3-Aminophenylboronic acid (m-Aminophenylboronic acid) is a phenylboronic acid derivative. 3-Aminophenylboronic acid reacts covalently with cis-diol groups of glycoproteins, enabling selective capture and detection of glycoproteins through fluorescence quenching of APBA-functionalized copper nanoclusters .
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1 Cited Publications
Cat. No.: HY-Y0395
CAS No.: 25487-66-5
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CY7-N3 (Sulfo-Cyanine7-N3) is a cyanine7 azide fluorescent dye and clickable quencher. CY7-N3 quenches the fluorescence of unreacted Cy5-DBCO, serves as a click chemistry quencher in the organelle-selective click labeling combined with flow cytometry (O-ClickFC) procedure for alkyne-labeled Palmitic acid (HY-N0830) in hematopoietic stem and progenitor cells, and can serve as a prodrug model loaded into DNAzyme-gated mesoporous Silicon dioxide (HY-W019831) nanoparticles. CY7-N3 can be used for click chemistry labeling and fluorescence imaging studies .
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1 Cited Publications
Cat. No.: HY-W000897
CAS No.: 206658-89-1
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3-Aminophenylboronic acid monohydrate is a phenylboronic acid derivative. 3-Aminophenylboronic acid monohydrate reacts covalently with cis-diol groups of glycoproteins, enabling selective capture and detection of glycoproteins through fluorescence quenching of APBA-functionalized copper nanoclusters .
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1 Cited Publications
Cat. No.: HY-D1050
CAS No.: 82321-04-8
Synonyms: 6-(2,4-Dinitrophenyl)aminohexanoic acid, succinimidyl ester
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1 Cited Publications
Cat. No.: HY-W127832
CAS No.: 123148-15-2
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
