Technical Data

P4275-05-ML650
Clone Type
Monoclonal
Host
Mouse
Source
Human
Conjugate
MaxLight™650
Isotype
IgG1,k, IgG2b,k
Clone Number
PL6/PL2 (3G251)
Grade
Affinity Purified
Applications
FLISA IF IP WB
Crossreactivity
Hu Mo Rt Xe
Shipping Temp
Blue Ice
Storage Temp
4°C Do Not Freeze
Notes
Preservative Free
BSA Free
Mouse Anti-Plk (Polo-like Kinase) mixed clones (MaxLight 650)

MaxLight™ 650 is a new Far-IR stable dye conjugate comparable to Alexa Fluor™647, DyLight™649, Cy5™ and offers better labeling efficiency, brighter imaging and increased immunodetection. Absorbance (655nm); Emission (676nm); Extinction Coefficient 250,000.

Storage and Stability
Plk is a serine/threonine kinase which is highly homologous to the Drosophila serine/threonine kinase encoded by the mutant polo. Plk and polo encode proteins of similar size and possess a similar overall structure, with their catalytic domains located near the N-terminal region. In Drosophila, the polo kinase appears to be involved in cell cycle regulation and chromosome segregation, and homozygous mutations in polo results in the appearance of aberrant chromosome segregation and frequently lethal mitosis. Studies on mammalian cells indicate that Plk expression is restricted to proliferating cells. Consistent with this finding, Plk mRNA can be detected in most tissues during mammalian development; however, in adult tissues, its expression is restricted to the thymus and ovaries. Plk is related to several other serine/threonine kinases which include: Saccharomyces cerevisiae CDC5, murine Snk (serum-inducible kinase), murine Fnk (FGF-inducible kinase), and murine Sak (Snk/Plk-akin kinase. Plk protein levels are cell-cycle regulated with low levels of detected in G1 phase and higher levels detected in S and G2-M. Plk kinase activity is also cell-cycle regulated and is modulated, at least in part, by phosphorylation of Plk on one or more serine residues by an as yet unidentified kinase. Phosphorylation on serine serves to stimulate Plk kinase activity and results in slower migration of the Plk protein when analyzed by SDS-PAGE. Interestingly, activation of the Plk kinase activity parallels that of Cdc2; however, Cdc2 kinase is not thought to be directly responsible for Plk phosphorylation. Suitable for use in Immunofluorescence, FLISA, Western Blot and Immunoprecipitation. Other applications not tested. Immunofluorescence: 2-5ug/ml FLISA: 0.1-1ug/ml Western Blot: 1-2ug/ml Immunoprecipitation: 5ug Optimal dilutions to be determined by the researcher. HeLa, A431 and NIH 3T3 cells. Store product at 4°C in the dark. DO NOT FREEZE! Stable at 4°C for 12 months after receipt as an undiluted liquid. Dilute required amount only prior to immediate use. Further dilutions can be made in assay buffer. Caution: MaxLight™650 conjugates are sensitive to light. For maximum recovery of product, centrifuge the original vial prior to removing the cap.
Note: Applications are based on unconjugated antibody.
Immunogen
A His-tagged Plk fusion protein (C-term Plk1) corresponding to aa402-603 of the human Plk1 protein.
Form
Supplied as a liquid in PBS, pH 7.2. No preservatives added. Labeled with MaxLight™650.
Purity
Purified by Protein A affinity chromatography.
Specificity
Recognizes the human Plk1 protein at ~68kD. Species Crossreactivity: mouse, rat and Xenopus.

Intended for research use only. Not for use in human, therapeutic, or diagnostic applications.

References
1. Clay, F.J., et al. (1993) Proc. Natl. Acad. Sci. USA 90:4882-4886 2. Donohue, P.J., et al (1995) J. Biol Chem. 270:10351-10357. 3. Fode, C., etal (1994) Proc. Natl. Acad. Sci. USA 91:6388-6392. 4. Hamanaka, R., et al. (1994) Cell Growth and Differentiation 5:249-257. 5. Hamanaka, R., et al. (1995) J. Biol Chem. 270:21086-21091. 6. Holtrich, U., et al. (1994) Proc. Natl. Acad. Sci. USA 91:1736-1740. 7. Golsteyn, R.M et al. (1994) J. Cell Sci. 107:1509-1517. 8. Lake R.J., and Jelinek, W.R. (1993) Mol. Cell. Biol. 13:7793-7801. 9. Llamarazres, S., et al. (1991) Genes and Dev., 5:2153-2165. 10. Sunkel, C., and Glover, D.M. (1988) J. Cell. Sci. 89:25-38. 11. Zhou, B., et al., Proc. Natl. Acad. Sci. 95::6785-6790 (1998). 12. Ouyang, B., et al., J. Biol. Chem 272(45):28646-28651 (1997).
USBio References
No references available
United States Biological | 4 Technology Way | Salem, MA 01970
Phone 800-520-3011 | Fax 978-594-8052 | Website www.usbio.net