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To Purchase # 8020S

8020S 1 Kit (96 assays)

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ELISA Protocol

A. Reagent Preparation

  1. Bring all microwell strips to room temperature before use.
  2. Prepare 1X Wash Buffer by diluting 20X Wash Buffer (included in each kit) in Milli-Q or equivalently purified water.
  3. Dilute the 10X Cell Lysis Buffer #9803 to 1X in Milli-Q or equivalently purified water. 1 mM phenylmethylsulfonyl fluoride (PMSF) should be added fresh each time. This buffer can be stored at 4°C for short-term use (1–2 weeks).

B. Preparing Cell Lysates

  1. Plate cells of interest in 96-well plate (typically between 6-100 X 103 cells/well) and incubate overnight under appropriate cell culture conditions.
  2. Rinse cells with 200 µl warm PBS, then add test compounds in serum free mediums and incubate cells for the desired time period.
  3. Rinse cells twice with 200 µl ice cold PBS, and then add 100 µl/well 1X lysis buffer, keep cells on ice for 5 to 10 minutes.

NOTE: If cell debris is observed it can be removed by brief centrifugation of the plate and transfer of the clear lysates to a new 96 well plate.

C. Assay

  1. Bring all kit components to room temperature.
  2. Make cGMP standard in the 1X Cell Lysis buffer: Take 50 µl of the cGMP standard (5 µM) and add it to 450 µl diluent to get 500 nM cGMP. Perform a 1:3 serial dilution of this standard to get 160.7 nM, 55.6 nM, 18.5 nM, 6.2 nM, 2.1 nM, 0.7 nM,and 0 nM. The diluent without cGMP will serve as the 0 nM cGMP.

    NOTE: The standard curve is used to calculate the absolute amount of cGMP in the sample and is necessary for each assay.

  3. Add 25 µl of the HRP-linked cGMP solution and 25 µl sample to the cGMP assay plate. Cover the plate and incubate at room temperature for 3 hours on a horizontal orbital plate shaker.
  4. Discard plate contents and wash wells 4 times with 200 µl /well of 1X Wash Buffer. Make sure to discard all liquid after each wash but do not allow wells to completely dry.
  5. Prepare working solution by mixing equal parts Luminol/Enhancer Solution and Stable Peroxide Buffer.
  6. Add 50 µl of the Working Solution to each well.

Use a plate-based luminometer to measure Relative Light Units (RLU) at 425 nM within 1-10 minutes following addition of the substrate. Optimal signal intensity is achieved when read within 10 minutes.

protocol id: 507

Product Includes Quantity (with Count) Solution Color
cGMP Ab Coated Microwells 96 tests
cGMP-HRP Conjugate 5.5 ml Red
cGMP Standard 0.5 ml Colorless
Luminol/Enhancer Solution 3 ml Colorless
Stable Peroxide Buffer 3 ml Colorless
Sealing Tape 2 sheets
ELISA Wash Buffer (20X) 10 ml Colorless
Cell Lysis Buffer (10X) 9803 15 ml Yellowish

Product Description

The Cyclic GMP XP® Chemiluminescent Assay Kit is a competition enzyme-linked immunoassay used to determine cGMP levels in cells or tissues of interest. In this assay, cGMP found in the test sample competes with a fixed amount of HRP-linked cGMP for binding to an anti-cGMP XP® Rabbit mAb immobilized onto a 96-well plate. Following washing to remove excess sample cGMP and HRP-linked cGMP, chemiluminescent reagent is added for signal development. Because of the competitive nature of this assay, the magnitude of light emission, measured in relative light units (RLU), is inversely proportional to the quantity of sample cGMP. Measurement of light emmision using the cGMP Standard allows calculating the absolute amount of cGMP in a sample of interest.


Specificity / Sensitivity

The immunoreactivity of this kit was tested against the following: ADP, AMP, ATP, cAMP, cGMP, cIMP, cTMP, CTP, GDP, GMP, and GTP. Minor cross-reactivity was observed with cIMP, with over 100-fold higher sensitivity for cGMP compared to cIMP. No cross-reactivity was observed with any of the other factors tested. Kit sensitivity, as shown in Figure 1, demonstrates a dynamic range of 2 to 200 nM of cGMP. Changes in cellular cGMP levels following specific treatments are shown in Figure 2 (low passage RFL-6 cells).


Cyclic guanosine 3’,5’-monophosphate (cGMP) is a critical and multifunctional second messenger molecule involved in many signal transduction pathways in different cell types of almost all species (1). Intracellular cGMP is generated from GTP by guanylyl cyclase (GC) and degraded through phosphodiesterase (PDE) hydrolysis (1,2). Two distinctive families of GC have been identified: soluble guanylyl cyclases (sGC) that are nitric oxide-responsive and cell membrane-bound; and particulate guanylyl cyclases (pGC) that respond to diverse extracellular agonists including peptide hormones, bacterial toxins, and free radicals (2,3). Phosphodiesterases form a superfamily of 11 isoforms with different specificity to both cyclic adenosine 3’,5’-monophosphate (cAMP) and cGMP (4). Cyclic GMP regulates cellular physiology by activating cGMP-dependent kinase, modulating cGMP-dependent ion channels or transporters, and altering its own hydrolytic degradation by PDE (1,4). Because of the diversity of its effectors, cGMP plays an important role in regulating various pathological and physiological processes, such as vascular smooth muscle motility, intestinal fluid and electrolyte homeostasis, and retinal phototransduction (1,5).


1.  Domek-Łopacińska, K. and Strosznajder, J.B. (2005) J Physiol Pharmacol 56 Suppl 2, 15-34.

2.  Lucas, K.A. et al. (2000) Pharmacol Rev 52, 375-414.

3.  Potter, L.R. et al. (2006) Endocr Rev 27, 47-72.

4.  Matsumoto, T. et al. (2003) J Smooth Muscle Res 39, 67-86.

5.  Rybalkin, S.D. et al. (2003) Circ Res 93, 280-91.



For Research Use Only. Not For Use In Diagnostic Procedures.
Cell Signaling Technology® is a trademark of Cell Signaling Technology, Inc.
XP® is a trademark of Cell Signaling Technology, Inc.