Cell Signaling Technology

Product Pathways - PathScan ELISA

PathScan® Signaling Nodes II 4-Plex Array Kit #7139

Kit Includes Volume
Microtiter well plate having four capture antibodies spotted at the bottom of each well 1 96 well plate
Sample diluent buffer 10 milliliters
20X Wash buffer 50 milliliters
Detection antibody mix 5.5 milliliters
Streptavidin-HRP solution 5.5 milliliters
Sealing tape 2 sheets
Chemiluminescent substrate 5.5 milliliters each
10X Cell Lysis Buffer #9803 10 milliliters

Note: 12 8-well modules –Each module is designed to break apart for 8 tests.
Note: Kit should be stored at 4°C with the exception of Cell Lysis Buffer (10X), which is stored at –20°C (packaged separately).

Species Cross-Reactivity

H M

Reactivity Key:  H=Human  M=Mouse

Description

CST’s PathScan® Signaling Nodes II 4-Plex Array Kit is based upon the sandwich ELISA principle. Rather than one immobilized antibody, these PathScan® 4-Plex Array Kits contain four different antibodies in each well of a 96-well plate. This allows the researcher to measure four different target proteins from a single well simultaneously. In addition, the incorporation of multiple phospho-specific antibody pairs allows the researcher to measure the activation state of important signaling nodes. The PathScan® Signaling Nodes II 4-Plex Array Kit allows the detection of: Phospho-Akt1 (Ser473); Phospho-MEK1 (Ser217/221); Phospho-p44 MAPK (Thr202/Tyr204); and Total Akt1.Briefly, 4 capture antibodies with distinct target specificity have been spotted onto the bottom of each well of a microwell plate. After incubation with cell lysates, the spotted antibodies capture the target proteins. Following extensive washing, a mixture of detection antibodies is added to detect the captured target proteins. An HRP-linked secondary solution is then used to recognize the bound detection antibodies. Chemiluminescent HRP substrate is used to produce luminescent signal.

Specificity / Sensitivity

PathScan® Signaling Nodes II 4-Plex Array Kit detects endogenous levels of all target proteins. As shown in Figure 2, stimulation of NIH/3T3 cells with PDGF promotes phosphorylation of Akt at Ser473, p44 MAP kinase at Thr202/Tyr204 and MEK1 on Ser217/221. Levels of total Akt1 remain unchanged.

Necessary Equipment

Quansys Biosciences logo

Quansys imager (Cat # 104450GR) and Q-View Plus™ software (Quansys Biosciences, UT; www.quansysbio.com) are recommended for this assay kit for acquisition of the luminescent signal and quantification of spot intensity, respectively. Alternative imagers compatible with this array product are: Alpha Innotech Fluorchem SP; Bio-Rad Versa Doc 4000; Fujifilm LAS-3000; Kodak 4000 MM; UVP EC3 Biochemi.

Figure 1: Schematic representation of the position of targets in a single well.

Figure 2: NIH/3T3 cells were starved and stimulated with PDGF (100 ng/ml) for 5 minutes at 37°C. Lysates were analyzed using the PathScan® Signaling Nodes II 4-Plex Array Kit. Luminescent signals were acquired using a Quansys Biosciences imager. Spot intensity was quantified using Q-View™ software. The bar graph shows measurements of four different target proteins. Corresponding Western blots obtained with the same cell lysates are shown at the bottom.

Figure 3: Cell extracts from unstimulated or stimulated NIH/3T3 cells were applied to wells at increasing total protein concentrations and analyzed. Luminescent signals were acquired and spot intensity quantified. The graphs show the relationship between the total protein concentration and the resulting strength of the luminescent signal for each target.


Background

Cells must respond in an appropriate fashion to many complex signaling events. Extracellular signaling cues are organized into well defined signal transduction modules that control fundamental cellular behavior. Two prominent signaling modules that are among the best characterized are the p44/42 MAP kinase (ERK MAPK) and Akt signal transduction pathways. These signaling modules control cellular growth, proliferation, movement, survival, and death. The p44/42 MAPK is activated by a wide variety of extracellular signals including growth and neurotrophic factors, cytokiones, hormones, and neurotransmitters. p44/42 MAPK activation occurs through phosphorylation of theronine and tyrosine at the sequence T*EY* by a dual specificity kinase called MAP kinase kinase (MEK). The Akt protein kinase is generally activated in response to growth factor stimulation and phosphorylated on Ser473. Growth factor stimulation results in phosphorylation of S6 Ribosomal protein on Ser235/236, leading to an increase in protein synthesis and cell cycle progression. Phosphorylation levels of critical molecular switches such as MAPKs and Akt therefore serve as a reliable indicator of the activation state of the entire signaling module. The profiling of phosphorlation events using phospho-specific antibodies is now widely used to investigate diagnostic pathology (1,2). The PathScan® Signaling Nodes II 4-Plex Array Kit provides the researcher with means to profile numerous chemical compounds and obtain in-cell relative potency (3).

  1. Sheehan, K.M. et al. (2008) Oncogene 27, 323-31.
  2. Kreisberg, J.I. et al. (2004) Cancer Res 64, 5232-6.
  3. Gechtman Z. (2006) American Drug Discovery 1:1, 44-52

Application References

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Companion Products

Rabbit Monoclonals are produced under license (granting certain rights, including those under U.S. Patent No. 5,675,063) from Epitomics, Inc.

This product is for in vitro research use only and is not intended for use in humans or animals. This product is not intended for use as therapeutic or in diagnostic procedures.

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