| 货号 | 7333C |
| 描述 | The PathScan® Phospho-Met (panTyr) Sandwich ELISA Kit is a solid phase sandwich enzyme-linked immunosorbent assay (ELISA) that detects endogenous levels of Met when tyrosine phosphorylated. A Met Rabbit Antibody has been coated onto the microwells. After incubation with cell lysates, Met (phospho and nonphospho) is captured by the coated antibody. Following extensive washing, a Phospho-Tyrosine Mouse Detection Antibody is added to detect tyrosine phosphorylation of the captured Met 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 the absorbance for this developed color is proportional to the quantity of Met phosphorylated on tyrosine. Antibodies in kit are custom formulations specific to kit. |
| 反应种属 | Human |
| 应用 | ELISA |
| 目标/特异性 | CSTs PathScan® Phospho-Met (panTyr) Sandwich ELISA Kit #7333 detects Met when tyrosine phosphorylated. High levels of phospho-Met protein are detected in HCC827 cells where Met is constitutively phosphorylated (Figure 1). These high levels are abolished in HCC827 cells lysed without addition of phosphatase inhibitors* to the lysis buffer. The levels of total Met protein (phospho and nonphospho) as detected by PathScan® Total Met Sandwich ELISA Kit #7242 remain unchanged (Figure 1). This kit detects proteins from the indicated species, as determined through in-house testing, but may also detect homologous proteins from other species. * Phosphatase inhibitors include sodium pyrophosphate, β-glycerophosphate and Na3VO4. |
| 供应商 | CST |
| 背景 | Met, a high affinity tyrosine kinase receptor for hepatocyte growth factor (HGF, also known as scatter factor) is a disulfide-linked heterodimer made of 45 kDa α- and 145 kDa β-subunits (1,2). The α-subunit and the amino-terminal region of the β-subunit form the extracellular domain. The remainder of the β-chain spans the plasma membrane and contains a cytoplasmic region with tyrosine kinase activity. Interaction of Met with HGF results in autophosphorylation at multiple tyrosines, which recruit several downstream signaling components, including Gab1, c-Cbl, and PI3 kinase (3). These fundamental events are important for all of the biological functions involving Met kinase activity. The addition of a phosphate at cytoplasmic Tyr1003 is essential for Met protein ubiquitination and degradation (4). Phosphorylation at Tyr1234/1235 in the Met kinase domain is critical for kinase activation. Phosphorylation at Tyr1349 in the Met cytoplasmic domain provides a direct binding site for Gab1 (5). Altered Met levels and/or tyrosine kinase activities are found in several types of tumors, including renal, colon, and breast. Thus, Met is an attractive cancer therapeutic and diagnostic target (6,7). |
| 存放说明 | 4C |
| 参考文献 | Cooper, C.S. et al. (1984) Nature 311, 29-33. Bottaro, D.P. et al. (1991) Science 251, 802-4. Bardelli, A. et al. (1997) Oncogene 15, 3103-11. Taher, T.E. et al. (2002) J Immunol 169, 3793-800. Schaeper, U. et al. (2000) J Cell Biol 149, 1419-32. Eder, J.P. et al. (2009) Clin Cancer Res 15, 2207-14. Sattler, M. and Salgia, R. (2009) Update Cancer Ther 3, 109-118. |
Figure 1: Constitutive phosphorylation of Met in HCC827 cells lysed in the presence of phosphatase inhibitors (phospho lysate) is detected by PathScan® Phospho-Met (panTyr) Sandwich ELISA Kit #7333 (top, right). In contrast, a low level of phospho-Met protein is detected in HCC827 cells lysed without addition of phosphatase inhibitors to the lysis buffer (nonphospho lysate). Similar levels of total Met protein from either nonphospho or phospho lysates are detected by PathScan® Total Met Sandwich ELISA Kit #7242 (top, left). Absorbance at 450 nm is shown in the top figure, while the corresponding western blots using Phospho-Met (Tyr1234/1235) Antibody #3126 (right) or a total Met Antibody #4560 (left) are shown in the bottom figure.图1：用PathScan® Phospho-Met (panTyr) Sandwich ELISA Kit #7333能够在磷酸酶抑制剂处理后的HCC827细胞的裂解液中（磷酸化的裂解液）中检测到磷酸化的Met （上，右）。相比之下，没有磷酸酶抑制剂*存在时（非磷酸化的裂解液），仅能检测到低水平的phospho-HER2/ErbB2的表达。用PathScan® Total Met Sandwich ELISA Kit #7242则能在磷酸化和非磷酸化的裂解液中检测到近似水平的总Met的表达（上，左）。上图显示450nm处的吸光值，下图显示用Phospho-Met (Tyr1234/1235) Antibody #3126（右）或total Met Antibody #4560（左）进行免疫印迹检测的结果。 | |
Figure 2: The relationship between protein concentration of phospho or nonphospho lysates and the absorbance at 450 nm is shown. Unstarved HCC827 cells were cultured (85% confluence) and lysed with or without addition of phosphatase inhibitor to the lysis buffer (phospho or nonphospho lysate).图2：磷酸化或非磷酸化的裂解中蛋白含量和450nm吸光值之间的关系。未饥饿的HCC827细胞在85%满时收样，并用加入或未加磷酸酶抑制剂的裂解液进行处理（磷酸化或非磷酸化）。 |
