Fascin-1 Protein: wild-type (Human recombinant)


Product Uses

• Study actin-bundling activity.
• Identification of compounds that inhibit actin and fascin 1 actin-bundling activity.
• Biochemical characterization of fascin 1 protein interactions
• Western blot standard


The wild-type human fascin 1 protein has been produced in a bacterial expression system. The recombinant protein contains no tag. The molecular weight of fascin is approximately 54 kDa and it is supplied as a white lyophilized powder.

Storage and Reconstitution

Before reconstitution, briefly centrifuge to collect the product at the bottom of the tube. The protein should be reconstituted to 5 mg/ml with the addition of 20 µl of Milli-Q water (100 µg size).  When reconstituted, the protein will be in the following buffer: 20 mM Tris pH 8.0, 150 mM NaCl, 2 mM CaCl2, 5% (w/v) sucrose, and 1% (w/v) dextran. In order to maintain high biological activity of the protein, it is strongly recommended that the protein solution be supplemented with DTT to 1 mM final concentration, aliquoted into "experiment-sized" amounts, snap frozen in liquid nitrogen, and stored at -70°C. The protein is stable for six months if stored at -70°C. The protein should not be exposed to repeated freeze-thaw cycles. The lyophilized protein is stable at 4°C desiccated (<10% humidity) for one year.


Protein purity is determined by scanning densitometry of Coomassie Blue-stained protein on a 4-20% polyacrylamide gradient gel. Fascin 1 protein was determined to be >95% pure. (see Figure 1 Below).

Figure 1.  Fascin 1 Protein Purity Determination.  A 10 µg sample of recombinant fascin 1 protein (molecular weight approx. 54 kDa) was separated by electrophoresis in a 4-20% SDS-PAGE system and stained with Coomassie Blue. Protein quantitation was determined using the Precision Red Protein Assay Reagent (Cat. # ADV02).  Mark12 molecular weight markers are from Life Technologies Inc.


Fluorescence Microscopy Images of Actin-Bundling Assay with Fascin 1.


Figure Legend: Actin filaments alone and with fascin 1 stained with Acti-stainTM 488 Phalloidin as described in the method. Actin filaments were observed under a fluorescent microscope with a 480Ex/535Em filter set, a digital CCD camera, and 63x objective.

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AuthorTitleJournalYearArticle Link
Sakamoto, Ryota et al.F-actin architecture determines the conversion of chemical energy into mechanical workNature Communications 2024ISSN 2041--1723

If you have any questions concerning this product, please contact our Technical Service department at tservice@cytoskeleton.com