Revision 1

#7105Store at +4C

 

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Species Cross Reactivity

H Mk

UniProt ID:

#P04637, #Q92934, #P42574, #P09874

Entrez-Gene Id:

#7157, #572, #836, #142

Cell Signaling Technology

Orders: 877-616-CELL (2355) [email protected]

Support: 877-678-TECH (8324)

Web: [email protected] cellsignal.com

3 Trask LaneDanversMassachusetts01923USA
For Research Use Only. Not for Use in Diagnostic Procedures.
Product Includes Product # Quantity Color Storage Temp
Apoptosis Multi-Target 43136 96 tests +4C
TMB Substrate 7004 11 ml Colorless +4C
STOP Solution 7002 11 ml Colorless +4C
Sealing Tape 54503 2 ea +4C
ELISA Wash Buffer (20X) 9801 25 ml Colorless +4C
ELISA Sample Diluent 11083 25 ml Blue +4C
Cell Lysis Buffer (10X) 9803 15 ml Yellowish -20C

*The microwell plate is supplied as 12 8-well modules - Each module is designed to break apart for 8 tests.

Description

CST’s PathScan® Apoptosis Multi-Target Sandwich ELISA Kit is a solid phase sandwich enzyme-linked immunosorbent assay (ELISA) that combines the reagents necessary to detect endogenous levels of p53 protein, phospho-p53 protein (Ser15), Bad, phospho-Bad (Ser112), Cleaved Caspase-3 (Asp175) and Cleaved PARP (Asp214). These molecules represent key signaling proteins in pathways controlling survival and apoptosis. Sixteen assays are provided for each target protein. Specific assay formulations for the indicated target proteins can be found in the datasheets associated with the individual sandwich ELISA kits*. Briefly, a capture antibody** has been coated onto the microwells. After incubation with cell lysates, the target protein is captured by the coated antibody. Following extensive washing, a detection antibody** is added to detect the captured target protein. An HRP-linked secondary antibody is then used to recognize the bound detection antibody. HRP substrate, TMB, is added to develop color. The magnitude of absorbance for this developed color is proportional to the quantity of bound target protein.
*See companion products.
**Antibodies in kit are custom formulations specific to kit.

Specificity/Sensitivity

CST's PathScan® Apoptosis Multi-Target Sandwich ELISA Kit #7105 detects endogenous levels of six proteins: total p53, phospho-p53 (Ser15), total Bad, phospho-Bad (Ser112), cleaved caspase-3 (Asp175) and cleaved PARP (Asp214). Activation of these proteins can be observed over time in response to toxic chemical compounds. As shown in Figures 1 and 2, both doxorubicin and staurosporine can induce apoptosis in HeLa cells, evidenced by increased levels of cleaved PARP and caspase-3. However, treatment with doxorubicin, which damages cellular DNA, induces p53 phosphorylation at Ser15 and stabilizes p53, while treatment with staurosporine, a kinase inhibitor, has no effect on p53 phosphorylation. While total Bad and phospho-Bad (Ser112) levels are relatively consistent after doxorubicin treatment, a gradual decline of both targets was observed after staurosporine treatment. COS cells are resistant to apoptosis due to high constitutive levels of p53. Therefore, the same dose of doxorubicin applied to HeLa cells only induces low amounts of apoptosis in these cells as evidenced by cleaved caspase-3 and cleaved PARP protein levels (Figure 3). The relationship between the protein concentration of the lysate and the absorbance at 450 nm can be found in the datasheets associated with the individual PathScan® Sandwich ELISA Kits*.
*See companion products.
This kit detects proteins from the indicated species, as determined through in-house testing, but may also detect homologous proteins from other species.

Background

Apoptosis is a regulated physiological process leading to cell death. Caspases, a family of cysteine acid proteases, are central regulators of apoptosis. Initiator caspases (including 8, 9, 10, and 12) are closely coupled to proapoptotic signals. Once activated, these caspases cleave and activate downstream effector caspases (including 3, 6, and 7), which in turn cleave cytoskeletal and nuclear proteins like PARP, α-fodrin, DFF, and lamin A and induce apoptosis. Cytochrome c released from mitochondria is coupled to the activation of caspase-9, a key initiator caspase (1). Proapoptotic stimuli include FasL, TNF-α, DNA damage and ER stress. Fas and TNFR activate caspase-8 and -10 (2), DNA damage leads to the activation of caspase-9 and ER stress leads to the calcium-mediated activation of caspase-12 (3). The inhibitor of apoptosis protein (IAP) family includes XIAP and survivin and functions by binding and inhibiting several caspases (4,5). Smac/Diablo, a mitochondrial protein, is released into the cytosol upon mitochondrial stress and competes with caspases for binding of IAPs. The interaction of Smac/Diablo with IAPs relieves the inhibitory effects of IAPs on caspases (6).

  1. Baker, S.J. and Reddy, E.P. (1998) Oncogene 17, 3261-3270.
  2. Budihardjo, I. et al. (1999) Annu. Rev. Cell Dev. Biol. 15, 269-290.
  3. Nakagawa, T. et al. (2000) Nature 403, 98-103.
  4. Deveraux, Q. L. et al. (1998) EMBO J. 17, 2215-2223.
  5. Li, F. et al. (1998) Nature 396, 580-584.
  6. Du, C. et al. (2000) Cell 102, 33-42.

Background References

    Cross-Reactivity Key

    H: human M: mouse R: rat Hm: hamster Mk: monkey Vir: virus Mi: mink C: chicken Dm: D. melanogaster X: Xenopus Z: zebrafish B: bovine Dg: dog Pg: pig Sc: S. cerevisiae Ce: C. elegans Hr: horse GP: Guinea Pig Rab: rabbit All: all species expected

    Trademarks and Patents

    Cell Signaling Technology is a trademark of Cell Signaling Technology, Inc.
    PathScan is a registered trademark of Cell Signaling Technology, Inc.
    All other trademarks are the property of their respective owners. Visit cellsignal.com/trademarks for more information.

    Limited Uses

    Except as otherwise expressly agreed in a writing signed by a legally authorized representative of CST, the following terms apply to Products provided by CST, its affiliates or its distributors. Any Customer's terms and conditions that are in addition to, or different from, those contained herein, unless separately accepted in writing by a legally authorized representative of CST, are rejected and are of no force or effect.

    Products are labeled with For Research Use Only or a similar labeling statement and have not been approved, cleared, or licensed by the FDA or other regulatory foreign or domestic entity, for any purpose. Customer shall not use any Product for any diagnostic or therapeutic purpose, or otherwise in any manner that conflicts with its labeling statement. Products sold or licensed by CST are provided for Customer as the end-user and solely for research and development uses. Any use of Product for diagnostic, prophylactic or therapeutic purposes, or any purchase of Product for resale (alone or as a component) or other commercial purpose, requires a separate license from CST. Customer shall (a) not sell, license, loan, donate or otherwise transfer or make available any Product to any third party, whether alone or in combination with other materials, or use the Products to manufacture any commercial products, (b) not copy, modify, reverse engineer, decompile, disassemble or otherwise attempt to discover the underlying structure or technology of the Products, or use the Products for the purpose of developing any products or services that would compete with CST products or services, (c) not alter or remove from the Products any trademarks, trade names, logos, patent or copyright notices or markings, (d) use the Products solely in accordance with CST Product Terms of Sale and any applicable documentation, and (e) comply with any license, terms of service or similar agreement with respect to any third party products or services used by Customer in connection with the Products.

    Revision 1
    #7105

    PathScan® Apoptosis Multi-Target Sandwich ELISA Kit

    PathScan® Apoptosis Multi-Target Sandwich ELISA Kit: Image 1 Expand Image
    Figure 1. Treatment of HeLa cells with doxorubicin induces phosphorylation of p53 at Ser15, as well as cleavage of PARP and caspase-3 as detected by PathScan® Apoptosis Multi-Target Sandwich ELISA Kit #7105 and Western analysis. HeLa cells (80-90% confluent) were starved overnight and stimulated with doxorubicin (5 μM at 37ºC for indicated times). Lysates were assayed at a protein concentration of 1 mg/ml. The absorbance readings at 450 nm are shown as a 3-dimensional representation in the left panel, while the corresponding Western blots are shown in the right panel. Antibodies used for Western analysis include Phospho-p53 (Ser15) Antibody #9284, p53 Antibody #9282, Cleaved Caspase-3 (Asp175) Antibody #9661 and PARP Antibody #9542. Total Bad and phospho-Bad (Ser112) proteins were not detected by Western due to low endogenous levels in HeLa cells.
    PathScan® Apoptosis Multi-Target Sandwich ELISA Kit: Image 2 Expand Image
    Figure 2. Treatment of HeLa cells with staurosporine induces cleavage of PARP and caspase-3 but not phosphorylation of p53 at Ser15 as detected by PathScan® Apoptosis Multi-Target Sandwich ELISA Kit #7105 and Western analysis. HeLa cells (80-90% confluent) were starved overnight and stimulated with staurosporine (2 μM at 37ºC for indicated times). Lysates were assayed at a protein concentration of 1 mg/ml. The absorbance readings at 450 nm are shown as a 3-dimensional representation in the left panel, while the corresponding Western blots are shown in the right panel. The antibodies used for the Western analyses include Phospho-p53 (Ser15) Antibody #9284, p53 Antibody #9282, Cleaved Caspase-3 (Asp175) Antibody #9661 and PARP Antibody #9542. Total Bad and Phospho-Bad (Ser112) proteins were not detected by Western due to low endogenous levels in HeLa cells.
    PathScan® Apoptosis Multi-Target Sandwich ELISA Kit: Image 3 Expand Image
    Figure 3. Treatment of COS cells with doxorubicin induces low levels apoptosis as detected by PathScan® Apoptosis Multi-Target Sandwich ELISA Kit #7105 and Western analysis. COS cells (80-90% confluent) were starved overnight and stimulated with doxorubicin (5 μM for at 37ºC for indicated times). Lysates were assayed at a protein concentration of 1 mg/ml. The absorbance readings at 450 nm are shown as a 3-dimensional representation in the left panel, while the corresponding Western blots are shown in the right panel. The antibodies used for the Western analyses include Phospho-p53 (Ser15) Antibody #9284, p53 Antibody #9282, Cleaved Caspase-3 (Asp175) Antibody #9661, PARP Antibody #9542, Phospho-Bad (Ser112) (7E11) Mouse mAb #9296 and Bad Antibody #9292.
    PathScan® Apoptosis Multi-Target Sandwich ELISA Kit: Image 4 Expand Image
    Figure 4. Schematic representation of a 96-well plate depicting the color-code of the reagents used to detect endogenous levels of Phospho-p53 (Ser15) (orange; 1 & 2), p53 (yellow; 3 & 4), Cleaved Caspase 3 (Asp175) (purple; 5 & 6), Cleaved PARP (Asp214) (green; 7 & 8), Phospho-Bad (Ser112) (pink; 9 & 10) and Bad protein (grey; 11 & 12).