Revision 1
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 Mol. Wt Isotype/Source
E-Cadherin (24E10) Rabbit mAb 3195 20 µl 135 kDa Rabbit IgG
p53 (7F5) Rabbit mAb 2527 20 µl 53 kDa Rabbit IgG
Stathmin Antibody 3352 20 µl 19 kDa Rabbit 
BRCA1 Antibody 9010 20 µl 220 kDa Rabbit 
Phospho-Akt (Ser473) (D9E) XP® Rabbit mAb 4060 20 µl 60 kDa Rabbit IgG
PTEN (138G6) Rabbit mAb 9559 20 µl 54 kDa Rabbit IgG
Phospho-Estrogen Receptor α (Ser167) (D1A3) Rabbit mAb 5587 20 µl 66 kDa Rabbit IgG
HER2/ErbB2 (D8F12) XP® Rabbit mAb 4290 20 µl 185 kDa Rabbit IgG
Anti-rabbit IgG, HRP-linked Antibody 7074 100 µl Goat 

Please visit cellsignal.com for individual component applications, species cross-reactivity, dilutions, protocols, and additional product information.

Description

The Oncogenes and Tumor Suppressor Antibody Sampler Kit offers an economical means of investigating proteins commonly involved in the biological pathways behind oncogenesis, tumor metastasis, and cancer pathology. The kit contains enough primary and secondary antibody to perform four western blot experiments with each antibody.

Storage

Supplied in 10 mM sodium HEPES (pH 7.5), 150 mM NaCl, 100 µg/ml BSA, 50% glycerol and less than 0.02% sodium azide. Store at –20°C. Do not aliquot the antibody.

Background

Oncogenesis is a multistep process leading to sequential alterations in several oncogenes, tumor-suppressor genes, and microRNA genes (1,2). These alterations often disrupt the expression, function, and/or activity of proteins regulating cell growth and programmed cell death. Many of the molecular mechanisms and biological pathways driving oncogenesis and cancer pathology have been identified. The signal transduction pathways regulating apoptosis, cell-cycle progression, cell adhesion, cell migration, and DNA damage responses are often disrupted. HER2/ErbB2 (3), E-Cadherin (4), p53 (5,6), Stathmin (7), BRCA1 (8,9), Akt (10), PTEN (11), and Estrogen Receptor α (12) function in many of these pathways.

  1. Berger, A.H. et al. (2011) Nature 476, 163-9.
  2. Peltomäki, P. (2012) Exp Cell Res 318, 299-310.
  3. Dittadi, R. and Gion, M. (2000) J Natl Cancer Inst 92, 1443-4.
  4. Hazan, R.B. et al. (2004) Ann N Y Acad Sci 1014, 155-63.
  5. Rahman, N. and Stratton, M.R. (1998) Annu Rev Genet 32, 95-121.
  6. Freed-Pastor, W.A. and Prives, C. (2012) Genes Dev 26, 1268-86.
  7. Belletti, B. and Baldassarre, G. (2011) Expert Opin Ther Targets 15, 1249-66.
  8. Gayther, S.A. et al. (1999) Am J Hum Genet 65, 1021-9.
  9. Scully, R. and Livingston, D.M. (2000) Nature 408, 429-32.
  10. Jazirehi, A.R. et al. (2012) Am J Cancer Res 2, 178-91.
  11. Saal, L.H. et al. (2008) Nat Genet 40, 102-7.
  12. Pópulo, H. et al. (2012) Int J Mol Sci 13, 1886-918.

Background References

    Trademarks and Patents

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

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