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Checkpoint Signaling and DNA Repair Interactive Pathway

Kit Resource
  PCNA ELISA Kit
Cat. No. QIA59  
All Categories » Calbiochem » Kits and Tools » Cell Cycle and Cell Proliferation Assays

Format: 96-well strip plate
Form: 96 Tests
Detection Method: Colorimetric
Species Reactivity: human, mouse, rat
Specificity: Human PCNA protein
Sensitivity: 0.5 U/ml of PCNA
Assay Range: 1.875 - 30 U/ml
Unit Definition: One unit (U) is defined as the amount of PCNA measured from ~ 2.6 x 103 SW620 cells.
Assay Time: 3.5 h
Sample Type: Cell lysates, tissue culture media , serum, or plasma
Kit Contents: 96-Well Removable Strip Plate, 2 vials of PCNA Standard, Detector Antibody, 400X Conjugate, Conjugate Diluent, Substrate, Sample Diluent, 20X Plate Wash Concentrate, Antigen Extraction Agent, Stop Solution, Plate Sealers, and a user protocol.
Comments: Fast, sensitive assay for the in vitro quantitation of PCNA protein. The kit has broad reactivity, and is suitable to detect PCNA in autoimmune sera samples. The assay was validated using the BrdU Cell Proliferation Assay (Cat. No. QIA58).
Proliferating cell nuclear antigen (PCNA) has no known enzymatic activity; however, it can interact with a variety of proteins and regulate their activities. These varied interactions with DNA metabolic proteins imply that PCNA is a central factor for the coordination of DNA replication, DNA repair, epigenetic inheritance, and cell-cycle control.
Ref.: Kelman, Z. and J. Hurwitz, 1998. Trends Biochem. Sci. 23, 236. Montecucco, A., et al. 1998. The EMBO Journal 17, 3786. Oku, T., et al. 1998. Genes Cells 3, 357. Waga, S. and B. Stillman, 1998. Annu. Rev. Biochem. 67, 721. Jonsson ZO and H. U, 1997. Bioessays 19, 967. Prosperi, E., 1997. Prog. Cell Cycle Res. 3, 19. Gulbis, J., et al. 1996. Cell, 87, 297. Brott, D.A., et al. 1993. J. Cell. Biochem. 52, 362.
R: 23/24/25-35-36/37/38-40-43; S: 26-36/37/39-45

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Graph 1. Detection of changes in PCNA levels after phorbol ester (PMA) induced growth arrest by Cat. No. QIA59. Macrophage-like differentiation can be induced in HL-60 cells by PMA. HL-60 cells were plated at 2 x 104 cells per well and various concentrations of PMA were added for a dose-response study. Cells were incubated for 96 hours, then assayed as described.


Standard Curve. The mean signal of each standard run in replicates of four in eight assays using two different lots of plates and two different lots of detector antibody.

Related Literature:

DNA Repair Pathway Poster

Cell Proliferation Assay Flyer

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QIA59: PCNA ELISA Kit - English
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