Amplex™ Acetylcholine/Acetlycholinesterase Assay Kit
Amplex™ Acetylcholine/Acetlycholinesterase Assay Kit
Invitrogen™

Amplex™ Acetylcholine/Acetlycholinesterase Assay Kit

The Amplex™ Red Acetylcholine/Acetylcholinesterase Assay Kit provides an ultrasensitive method for detecting acetylcholinesterase (AChE) activity in a fluorescence microplate readerRead more
Have Questions?
Catalog NumberQuantity
A12217500 Assays
Catalog number A12217
Price (CLP)
524.617
Each
Add to cart
Quantity:
500 Assays
Price (CLP)
524.617
Each
Add to cart
The Amplex™ Red Acetylcholine/Acetylcholinesterase Assay Kit provides an ultrasensitive method for detecting acetylcholinesterase (AChE) activity in a fluorescence microplate reader or fluorometer.

See our complete line of Fluorescence Microplate assays.

• Detect AChE activity levels as low as 0.002 U/mL in one hour
• Detect acetylcholine levels as low as 0.3 μM using excess AChE
• Achieve detection ranges of 0.3 μM to 100 μM acetylcholine
• Format allows for multiple time point measurements
• Designed for minimal autofluorescence interference

AChE activity is monitored indirectly using 10-acetyl-3,7-dihydroxyphenoxazine (Amplex™ Red reagent), a sensitive fluorogenic probe for hydrogen peroxide. AChE converts the acetylcholine substrate to choline, which is then oxidized by choline oxidase to betaine and hydrogen peroxide. In the presence of horseradish peroxidase, hydrogen peroxide reacts with the Amplex™ Red reagent in a 1:1 stoichiometric ratio to generate the highly fluorescent product resorufin.

Because resorufin has absorption and fluorescence emission maxima of approximately 571 nm and 585 nm, respectively, there is little interference from autofluorescence in most biological samples. Experiments with purified AChE from electric eel indicate that the Amplex™ Red Acetylcholine/Acetylcholinesterase Assay Kit can detect AChE levels as low as 0.002 U/mL using a reaction time of one hour. By providing an excess of AChE in the assay, the kit can also be used to detect acetylcholine levels as low as 0.3 μM, with a range of detection from 0.3 μM to 100 μM acetylcholine.

Use Amplex™ Red Assays for a Broad Range of Investigations
A wide variety of validated Amplex™ Red assays are available for studying cell signaling and lipids, neurobiology, inflammation and immune function, and metabolism. We also offer Amplex™ UltraRed Reagent (Cat. No. A36006), a second-generation reagent providing greater sensitivity and brighter fluorescence, and the Amplex™ Red/UltraRed Stop Reagent (Cat. No. A33855). The 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 three hours. Custom assay design and packaging are also available.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Detection MethodFluorescence Intensity
Quantity500 Assays
Shipping ConditionRoom Temperature
Substrate PropertiesMolecular Substrate
Substrate TypeHRP (Horseradish Peroxidase) Substrate, Acetylcholinesterase Substrate
Target EnzymeAcetylcholinesterase
For Use With (Application)Acetylcholine/Acetlycholinesterase Assay
For Use With (Equipment)Fluorescence Microplate Reader
Product LineAmplex
Product TypeAmplex Red Assay Kit
Unit SizeEach
Contents & Storage
Store in freezer -5°C to -30°C and protect from light.

Frequently asked questions (FAQs)

I'm using an Amplex Red kit, the reagent changes color to pink almost immediately in my own Krebs-Ringer buffer but not in HBSS. Why is this?

The components of Krebs-Ringer buffer (salts) should not cause oxidation of the Amplex reagent (which, in the presence of peroxidase and H2O2 oxidizes to resorufin, which is pink in color and fluorescent). Try water alone (the water used to make the Krebs-Ringer buffer). Since Hank's Buffered Saline Solution is typically purchased rather than made in the lab, it likely would not have the same contaminant. Another option is to degas the buffer prior to use to removed dissolved oxygen radicals.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

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.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

Citations & References (8)

Citations & References
Abstract
G-CSF rescues the memory impairment of animal models of Alzheimer's disease.
Authors:Tsai KJ, Tsai YC, Shen CK,
Journal:J Exp Med
PubMed ID:17517969
'Most of the current clinical treatments for Alzheimer''s disease (AD) are largely symptomatic and can have serious side effects. We have tested the feasibility of using the granulocyte colony-stimulating factor (G-CSF), which is known to mobilize hematopoietic stem cells (HSCs) from the bone marrow into the peripheral blood, as a ... More
The effects of anticholinergic insecticides on human mesenchymal stem cells.
Authors:Hoogduijn MJ, Rakonczay Z, Genever PG
Journal:Toxicol Sci
PubMed ID:16960032
'Mesenchymal stem cells (MSCs) are located primarily in the bone marrow and are characterized by their capacity to differentiate into mesenchymal lineages such as bone, fat, and cartilage in response to appropriate signals. Several signaling mechanisms act to control MSC survival, proliferation, and differentiation, and failure or disruption of these ... More
Enhanced purinergic contractile responses and P2X1 receptor expression in detrusor muscle during cycles of hypoxia-glucopenia and reoxygenation.
Authors:Elliott RA, Tonnu A, Ghaffar N, Taylor AH, Tincello DG, Norman RI,
Journal:
PubMed ID:23975903
'Bladders from patients with detrusor overactivity have an increased atropine-resistant contractile response to nerve stimulation. The bladder has also been shown to be very susceptible to hypoxia-glucopenia and reperfusion injury, leading to the hypothesis that episodes of hypoxia-glucopenia and reoxygenation result in increased atropine-resistant responses to nerve stimulation in the ... More
Role of pancreatic cancer-derived exosomes in salivary biomarker development.
Authors:Lau C, Kim Y, Chia D, Spielmann N, Eibl G, Elashoff D, Wei F, Lin YL, Moro A, Grogan T, Chiang S, Feinstein E, Schafer C, Farrell J, Wong DT,
Journal:
PubMed ID:23880764
'Recent studies have demonstrated that discriminatory salivary biomarkers can be readily detected upon the development of systemic diseases such as pancreatic cancer, breast cancer, lung cancer, and ovarian cancer. However, the utility of salivary biomarkers for the detection of systemic diseases has been undermined due to the absence of the ... More
Butyrate enemas enhance both cholinergic and nitrergic phenotype of myenteric neurons and neuromuscular transmission in newborn rat colon.
Authors:Suply E, de Vries P, Soret R, Cossais F, Neunlist M,
Journal:Am J Physiol Gastrointest Liver Physiol
PubMed ID:22492692
'Postnatal changes in the enteric nervous system (ENS) are involved in the establishment of colonic motility. In adult rats, butyrate induced neuroplastic changes in the ENS, leading to enhanced colonic motility. Whether butyrate can induce similar changes during the postnatal period remains unknown. Enemas (Na-butyrate) were performed daily in rat ... More