- PC10 (See other available formats)
- Regulatory Status
- Other Names
- Proliferating Cell Nuclear Antigen, DNA Polymerase δ Auxiliary Protein
- Mouse IgG2a, κ
- Ave. Rating
- Submit a Review
- Product Citations
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The PC10 monoclonal antibody reacts with proliferating cell nuclear antigen also known as PCNA or the DNA polymerase δ auxiliary protein. PCNA is a 36 kD trimeric ring that acts as a DNA-polymerase sliding clamp expressed in the nucleus of all proliferating cells. A prime function of PCNA appears to be increasing DNA polymerase δ processibility during elongation of the leading strand. PCNA is a useful marker for DNA synthesis and is highly conserved among most species, thus highlighting the very broad reactivity of this antibody.Product Details
- Human, Mouse, Rat, Cross-Reactivity: Other species
- Antibody Type
- Host Species
- Recombinant rat PCNA
- Phosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
- The antibody was purified by affinity chromatography, and conjugated with biotin under optimal conditions.
- 0.5 mg/mL
- Storage & Handling
- The antibody solution should be stored undiluted between 2°C and 8°C. Do not freeze.
ICFC - Quality tested
- Recommended Usage
Each lot of this antibody is quality control tested by immunofluorescent intracellular staining with flow cytometric analysis. Please follow the Cell Fixation and Permeabilization Protocol Using 70% Ethanol. For flow cytometric staining, the suggested use of this reagent is ≤ 0.125 µg per million cells in 100 µL volume. It is recommended that the reagent be titrated for optimal performance for each application.
- Application Notes
Additional reported applications (for the relevant formats) include: immunohistochemical staining2,5,6 of acetone-fixed frozen sections and formalin-fixed paraffin-embedded tissue sections, immunoprecipitation, intracellular flow cytometry3, immunofluorescence microscopy9, and Western blotting10.
(PubMed link indicates BioLegend citation)
- Ogata K, et al. 1985. J. Immunol. 135:2623.
- Garcia R, et al. 1989. Am. J. Pathol. 134:733.
- Landberg G, et al. 1990. Exp. Cell. Res. 187:111.
- Waseem N, et al. 1990. J. Cell Sci. 96:121.
- Yu C, et al. 1991. Histopathology 19:29.
- Wilkins B, et al. 1992. J. Pathol. 166:45.
- Yang W, et al. 1996. Human Pathol. 27:70.
- Galkowska H, et al. 1996. Vet. Immunol. Immunopathol. 53:329.
- Chou HYE, et al. 2006. J. Biol. Chem. 10:1074.
- Fulvio MD, et al. 2006. Oncogene 25:3932.
- Eswarakumar VP and Schlessinger J. 2007. Proc. Natl. Acad. Sci. USA 104:3937.
- Spector I, et al. 2012. PLoS One. 7:e41833. PubMed.
- Kim JH, et al. 2012. Immunol Lett. 147:18. PubMed.
- Satchi-Fainaro R, et al. 2012.PLoS One. 7:e44395. PubMed.
- Product Citations
AB_314694 (BioLegend Cat. No. 307904)
- DNA-polymerase sliding clamp, trimeric ring; 36 kD
Nuclear, all proliferating cells
- RAD6-dependent DNA repair pathway; increases DNA polymerase δ processibility during elongation of the leading strand
- PCNA, DNA polymerase δ, Rad6, Rad18, UBC9, MMS2, UBC13, RAD5
- Ubiquitination, Sumoylation
- Cell Type
- Neural Stem Cells
- Biology Area
- Cell Biology, Cell Cycle/DNA Replication, Immunology, Neuroscience, Neuroscience Cell Markers, Stem Cells
- Molecular Family
- Nuclear Markers
- Antigen References
1. Travali S, et al. 1989. J. Biol. Chem. 264:7466.
2. Waseem N, et al. 1990. J. Cell Sci. 96:121.
3. Hall P, et al. 1990. J. Pathol. 162:285.
4. Landberg G, et al. 1991. Cancer Res. 51:4570.
5. Woods A, et al. 1991. Histopathol. 19:21.
6. Hoege C, et al. 2002. Nature 419:135.
7. Yue H, et al. 2003. World J. Gastroenterol. 9:377.
8. Shan B, et al. 2003. J. Biol. Chem. 278:44009.
- Gene ID
- 5111 View all products for this Gene ID
- View information about PCNA on UniProt.org
- How many biotin molecules are per antibody structure?
- We don't routinely measure the number of biotins with our antibody products but the number of biotin molecules range from 3-6 molecules per antibody.
Compare Data Across All Formats
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Your actual data may vary due to variations in samples, target cells, instruments and their settings, staining conditions, and other factors.
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