Alexa Fluor 488 Tubulin
|048805||5 ul||0.1 mg|
Made in the USA
Store at -80°C and protect from light
For research use only.
Molecular Weight: ~110 kDa
Maximum Excitation/Emission: 494/517 nm
Labeling Stoichiometry: ~1.0 (check product label)
Form: green aqueous solution
Concentration: 20 mg/ml
Buffer Conditions: 50 mM K-Glutamate and 0.5 mM MgCl2 (pH 7.0)
Shipping: shipped on dry ice
Storage Conditions: store at -80˚C immediately
Shelf Life: check product label for expiration date
The microtubule network is a dynamic, force-generating cytoskeletal system essential for a number of basic cellular processes. Microtubules also serve as a track for kinesin and dynein motor proteins. As such, visualization of microtubules in real time, both in cells and in vitro, is critical in understanding cellular function and human disease. Tubulin protein, the basic component of microtubules, can be functionalized for visualization by covalent linkage with a fluorescent dye. Such modification must be performed in a way that maintains tubulin polymerization competency and functionality. The resulting labeled tubulin protein is useful in a number of applications ranging from live cell injection/imaging to in vitro nanoscale devices.
Labeled Tubulin-Alexa Fluor® 488 is generated by reacting Alexa Fluor® 488 succinimidyl ester with >99% pure tubulin protein, thereby covalently linking the dye to random tubulin protein surface lysines. Polymerization competency is maintained during the labeling process by reacting the dye with polymerized microtubules and subjecting the tubulin protein to a final polymerization/depolymerization cycle. The final labeled tubulin protein displays maximum absorption at 280 nm and 494 nm and a labeling stoichiometry ([dye]/[tubulin]) of ~1.0 as determined by spectroscopic analysis (Figure 1). Specific labeling stoichiometries are indicated on the product label. Labeled Tubulin-Alexa Fluor® 488 is commonly visualized with a FITC filter set with maximum excitation/emission wavelengths of 494/517 nm (Figure 2). The product is cryopreserved at 20 mg/ml in 50 mM K-Glutamate and 0.5 mM MgCl2 (pH=7.0).
Storage and Handling
Immediately transfer Labeled Tubulin-Alexa Fluor® 488 to -80°C upon receipt. Thaw only when ready to use by placing briefly in a 37°C water bath followed by immediate placement on ice. Clarify the labeled tubulin after thawing to remove any protein aggregates by centrifugation at 90k rpm (350k x g) for 5 minutes at 4°C. If desired, Labeled Tubulin-Alexa Fluor® 488 can be aliquoted into smaller experimental batches, frozen in liquid Nitrogen, and stored at -80°C with minor loss of polymerization competency. Avoid repeated freeze-thaw cycles and protect from light. View detailed storage and handling instructions.
Activity and Applications
Labeled Tubulin-Alexa Fluor® 488 will polymerize into microtubules when supplemented with guanosine-5’-triphosphate (GTP), warmed to 37˚C, and kept above its critical concentration. Polymerization activity is detectable in a variety of experimental systems including fluorescence microscopy assays, turbidity assays, and GTPase assays. Labeled tubulin protein is suitable for use in a variety of fluorescent experimental applications including live cell injection, and can be combined with unlabeled tubulin protein (Cycled Tubulin™ highly recommended; Cat. No. 032005) in generating fluorescent microtubules in vitro. Visit our protocols page for common microtubule polymerization protocols, including the generation of short, rigid microtubules stabilized by GMPCPP or long, flexible microtubules stabilized by taxol.
Labeled Tubulin-Alexa Fluor® 488 displays maximum absorption at 280 nm and 494 nm. Spectroscopic analysis reveals a peak at 280 nm and 494 nm, indicating absorption by the tubulin protein and Alexa Fluor® 488 dye, respectively.
Labeled Tubulin-Alexa Fluor® 488 is commonly visualized with a FITC filter set.
Taxol-stabilized microtubules at 5 mg/ml total tubulin protein with Labeled Tubulin-Alexa Fluor® 488 (Cat. No. 048805) and Cycled Tubulin™ (Cat. No. 032005) at a 1:5 ratio. Image acquired on a widefield fluorescence microscope.
- Keith, C.H., Feramiscoa, J.R., Shelanski, M. Direct visualization of fluorescein labeled microtubules in vitro and in microinjected fibroblasts. J. Cell Biol. 88, 234–240 (1981).
- Panchuk-Voloshina, N., Haugland, R.P., Bishop-Stewart, J., Bhalgat, M.K., Millard, P.J., Mao, F., Leung, W.Y. Alexa dyes, a series of new fluorescent dyes that yield exceptionally bright, photostable conjugates. J. Histochem. Cytochem. 47, 1179–1188 (1999).
- Malcos, J.L. and Hancock, W.O. Engineering tubulin: microtubule functionalization approaches for nanoscale device applications. Appl. Microbiol. Biotechnol. 90(1), 1-10 (2011).