Figure 1: Nonphospho and phospho-Smad2 proteins from untreated and TGF-β treated Mv1Lu cells detected by PathScan® Total Smad2 Sandwich ELISA kit #7244 showing similar optical density readings. OD 450 readings are shown in the top figure, while the corresponding Western blots using Smad2 Mouse mAb #3103 (left panel) or Phospho-Smad2 (Ser465/467) Antibody #3101 (right panel), are shown in the bottom figure.Learn more about how we get our images
Figure 2: The relationship between protein concentration of lysates from untreated and TGF-β-treated Mv1Lu cells and kit assay optical density readings. After starvation, Mv1Lu cells (85% confluence) were treated with TGF-β (100 ng/ml) for 15-30 min at 37°C, and then lysed.Learn more about how we get our images
Figure 3: Kit specificity demonstrated by Western blot analysis of the ELISA well captured protein is shown. Lysates were prepared from mink Mv1Lu cells and incubated in wells coated with capture antibody #3109. Wells were then washed, and captured protein was solubilized in SDS gel loading buffer. Mv1Lu lysate (lane 1) and captured protein (lane 2) were analyzed by Western blot using Smad2 Mouse mAb #3119. A single band corresponding to the Smad2 protein is detected in the captured material (lane 2).Learn more about how we get our images
|Product Includes||Volume||Solution Color|
|Smad2 Rabbit mAb Coated Microwells||96 tests|
|Smad2/3 Mouse Detection mAb||1 ea||Green (Lyophilized)|
|Anti-mouse IgG, HRP-linked Antibody (ELISA Formulated)||1 ea||Red (Lyophilized)|
|Detection Antibody Diluent||11 ml||Green|
|HRP Diluent||11 ml||Red|
|TMB Substrate 7004||11 ml|
|STOP Solution 7002||11 ml|
|ELISA Wash Buffer (20X)||25 ml|
|ELISA Sample Diluent||25 ml||Blue|
|Sealing Tape||2 ea|
|Cell Lysis Buffer (10X) 9803||15 ml|
NOTE: Prepare solutions with purified water.
*NOTE: Some PathScan® ELISA Kits may include HRP-Linked Streptavidin in place of HRP-Linked Antibody.
NOTE: Initial color of positive reaction is blue, which changes to yellow upon addition of STOP Solution.
posted November 2013
CST's PathScan® Total Smad2 Sandwich ELISA Kit is a solid phase sandwich enzyme-linked immunosorbent assay (ELISA) that detects endogenous levels of total Smad2 protein. A Smad2 Rabbit mAb has been coated onto the microwells. After incubation with cell lysates, both phospho- and nonphospho-Smad2 proteins are captured by the coated antibody. Following extensive washing, Smad2/3 Mouse mAb is added to detect both the captured phospho- and nonphospho-Smad2 protein. Anti-mouse IgG, HRP-linked Antibody is then used to recognize the bound detection antibody. HRP substrate, TMB, is added to develop color. The magnitude of optical density for this developed color is proportional to the quantity of total Smad2 protein.
Antibodies in kit are custom formulations specific to kit.
CST's PathScan® Total Smad2 Sandwich ELISA Kit #7244 detects endogenous levels of total Smad2 protein. As shown in Figure 1, both phospho- and nonphospho-Smad2 proteins from untreated and TGFβ treated MV1LU cell lysates are detected by this kit. In Figure 3, Western blot analysis of protein captured in the Smad2 Rabbit mAb #3109 coated microwell shows a single band corresponding to the Smad2 protein. Smad2 in Hela cells also can be detected by this kit (data not shown). This kit detects proteins from the indicated species, as determined through in-house testing, but may also detect homologous proteins from other species.
Human, Mouse, Mink
Members of the Smad family of signal transduction molecules are components of a critical intracellular pathway that transmit TGF-β signals from the cell surface into the nucleus. Three distinct classes of Smads have been defined: the receptor-regulated Smads (R-Smads), which include Smad1, 2, 3, 5, and 8; the common-mediator Smad (co-Smad), Smad4; and the antagonistic or inhibitory Smads (I-Smads), Smad6 and 7 (1-5). Activated type I receptors associate with specific R-Smads and phosphorylate them on a conserved carboxy terminal SSXS motif. The phosphorylated R-Smad dissociates from the receptor and forms a heteromeric complex with the co-Smad (Smad4), allowing translocation of the complex to the nucleus. Once in the nucleus, Smads can target a variety of DNA binding proteins to regulate transcriptional responses (6-8).
Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc. PathScan is a trademark of Cell Signaling Technology, Inc. U.S. Patent No. 7,429,487, foreign equivalents, and child patents deriving therefrom.
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|7244C||1 Kit (96 assays)||$ 489.0|