The category of compounds known as C14orf65 Activators would encompass molecules that engage with and upregulate the activity of the protein coded by the C14orf65 gene, a gene that is identified by its location on chromosome 14 and is characterized as an open reading frame. The protein encoded by C14orf65 is not thoroughly characterized, and its function within cellular processes remains largely unknown. Activators for this protein, therefore, would be designed to facilitate a greater understanding of its role by enhancing protein activity through various mechanisms such as increasing gene expression, stabilizing the protein structure, or promoting its interaction with other proteins or molecules within the cell. Identifying activators typically requires a comprehensive exploration of the protein's function, including its enzymatic activity, binding partners, and cellular localization. High-throughput screening methods would be employed to test large libraries of compounds, identifying those that can augment the activity of C14orf65. These screenings could be followed by secondary assays to verify the activity-boosting effects of the compounds in more detail.
Following the identification of initial hits in screening campaigns, the development of C14orf65 activators would enter a phase of meticulous optimization. Chemists would engage in synthesizing a series of derivatives based on the initial activator structures, aiming to refine their properties to enhance the specificity and potency of the interaction with the C14orf65 protein. This process often involves structure-activity relationship (SAR) studies, which systematically modify compound structures to determine the impact on protein activation. Techniques such as X-ray crystallography could be used to visualize the binding of activators to the C14orf65 protein, providing invaluable information to guide further modifications. Through iterative rounds of design, synthesis, and testing, the most active and selective compounds would be advanced, culminating in a set of precise molecular probes. These probes would be instrumental in dissecting the biological activities of the C14orf65 protein, yielding insights into its role in the cell and how it interacts within the broader network of cellular functions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $41.00 $74.00 $221.00 $247.00 $738.00 $1220.00 | 39 | |
Stabilizes microtubules and could induce cellular responses that upregulate microtubule-associated proteins. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $59.00 $85.00 $143.00 $247.00 | 38 | |
Destabilizes microtubules and could trigger a cellular response to upregulate microtubule-stabilizing proteins. | ||||||
Colchicine | 64-86-8 | sc-203005 sc-203005A sc-203005B sc-203005C sc-203005D sc-203005E | 1 g 5 g 50 g 100 g 500 g 1 kg | $100.00 $321.00 $2289.00 $4484.00 $18207.00 $34749.00 | 3 | |
Binds to tubulin, inhibiting microtubule polymerization, potentially affecting the expression of microtubule-associated proteins. | ||||||
Vinblastine | 865-21-4 | sc-491749 sc-491749A sc-491749B sc-491749C sc-491749D | 10 mg 50 mg 100 mg 500 mg 1 g | $102.00 $235.00 $459.00 $1749.00 $2958.00 | 4 | |
Inhibits microtubule formation and could lead to compensatory upregulation of proteins that stabilize microtubules. | ||||||
Epothilone B, Synthetic | 152044-54-7 | sc-203944 | 2 mg | $176.00 | ||
A microtubule stabilizer that might induce an increase in microtubule-associated proteins to balance the enhanced stabilization. | ||||||
Griseofulvin | 126-07-8 | sc-202171A sc-202171 sc-202171B | 5 mg 25 mg 100 mg | $85.00 $220.00 $598.00 | 4 | |
Disrupts microtubule function and could lead to changes in the expression of microtubule-associated genes. | ||||||
Podophyllotoxin | 518-28-5 | sc-204853 | 100 mg | $84.00 | 1 | |
An inhibitor of microtubule assembly, it could potentially influence the expression of proteins involved in microtubule dynamics. | ||||||