Amplex™ Red/UltraRed Stop Reagent is designed for use with the Amplex™ Red and Amplex™ UltraRed fluorogenic substrates and assay kits.Read more
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Catalog Number
Quantity
A33855
1 set
Catalog number A33855
Price (MXN)
-
Quantity:
1 set
Amplex™ Red/UltraRed Stop Reagent is designed for use with the Amplex™ Red and Amplex™ UltraRed fluorogenic substrates and assay kits. Amplex™ Red/UltraRed Stop Reagent provides convenience and control by allowing the fluorescence signal-generating reaction to be terminated at a user-determined time point. After addition of the stop reagent, the fluorescence signal remains stable for at least 3 hours.
Amplex™ UltraRed and Amplex™ Red assay kits are sensitive biomolecular assays based on hydrogen peroxide–generating enzyme systems linked to peroxidase–mediated oxidation of the fluorogenic Amplex™ UltraRed or Amplex™ Red substrates. Typically, detection reactions are performed in microplate wells and are initiated by adding the fluorogenic Amplex™ UltraRed or Amplex™ Red substrate, resulting in a continuous fluorescence increase that proceeds for 30 minutes or more. Ultimately, unknown analyte concentrations are determined by comparing fluorescence intensities measured at a certain time point during the reaction to parallel measurements at the same time point on standard samples of known concentration. Clearly, it is critical to ensure that the timing of the standard and unknown sample measurements is the same.
Amplex™ Red/UltraRed Stop Reagent is designed for use with both the Amplex™ Red and Amplex™ UltraRed fluorogenic substrates and assay kits. It is designed to terminate reactions containing up to 0.1 units/mL of horseradish peroxidase (HRP) and 5 μM hyrogen peroxide. The fluorescent signal then remains stable for at least 3 hours.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
FormLyophilized
Quantity1 set
Shipping ConditionRoom Temperature
For Use With (Application)Protein Assays
Product LineAmplex
Product TypeStop Solutions
Unit SizeEach
Contents & Storage
Store in refrigerator at 2°C to 8°C
Frequently asked questions (FAQs)
Can Amplex Red Assays be performed using cell lysates?
This is not recommended. The presence of endogenous proteases can complicate the assay by degrading the horseradish peroxidase (HRP). Endogenous peroxidases and antioxidants can modify the H2O2 required for the reaction, competing with HRP (and catalase) for the substrate.
The Amplex Red Assays are best performed with either purified enzymes or extracted H2O2 in a defined buffer system, extracellular solutions or body fluids (media, serum, etc.) that do not exhibit high levels of endogenous protease or oxidase activity and do not contain antioxidants.
Discovery of acetyl-coenzyme A carboxylase 2 inhibitors: comparison of a fluorescence intensity-based phosphate assay and a fluorescence polarization-based ADP Assay for high-throughput screening.
Authors:Liu Y, Zalameda L, Kim KW, Wang M, McCarter JD,
Journal:Assay Drug Dev Technol
PubMed ID:17477831
'Acetyl-coenzyme A carboxylase (ACC) enzymes exist as two isoforms, ACC1 and ACC2, which play critical roles in fatty acid biosynthesis and oxidation. Though each isoform differs in tissue and subcellular localization, both catalyze the biotin- and ATP-dependent carboxylation of acetyl-coenzyme A to generate malonyl-coenzyme A, a key metabolite in the ... More
Facile SNP detection using bifunctional, cross-linking oligonucleotide probes.
Authors:Peng X, Greenberg MM,
Journal:Nucleic Acids Res
PubMed ID:18281702
A facile, sensitive method for detecting specific sequences of oligonucleotides was developed. Detection of DNA sequences with single nucleotide discrimination is achieved by combining the selectivity of hybridization with an efficient cross-linking reaction. Readily synthesized bifunctional oligonucleotide probes containing a modified pyrimidine that is capable of forming interstrand cross-links under ... More
Enzymatic measurement of phosphatidic acid in cultured cells.
Authors:Morita SY, Ueda K, Kitagawa S,
Journal:J Lipid Res
PubMed ID:19369695
In this work, we developed a novel enzymatic method for measuring phosphatidic acid (PA) in cultured cells. The enzymatic reaction sequence of the method involves hydrolysis of PA to produce glycerol-3-phosphate (G3P), which is then oxidized by G3P oxidase to generate hydrogen peroxide. In the presence of peroxidase, hydrogen peroxide ... More
pLG72 modulates intracellular D-serine levels through its interaction with D-amino acid oxidase: effect on schizophrenia susceptibility.
Authors:Sacchi S, Bernasconi M, Martineau M, Mothet JP, Ruzzene M, Pilone MS, Pollegioni L, Molla G,
Journal:J Biol Chem
PubMed ID:18544534
Human genes coding for pLG72 and d-amino acid oxidase have recently been linked to the onset of schizophrenia. pLG72 was proposed as an activator of the human FAD-containing flavoprotein d-amino acid oxidase (hDAAO). In the brain this oxidizes d-serine, a potent activator of N-methyl-d-aspartate receptor. We have investigated the mechanistic ... More