Gas7 inhibitors represent a specialized class of chemical compounds that have gained recognition in the realm of molecular biology and cellular cytoskeletal regulation research. Gas7, or Growth Arrest-Specific 7, is a protein involved in various cellular processes, including cytoskeletal organization, cell morphology, and intracellular signaling. The term Gas7 inhibitors refers to a group of molecules meticulously designed to selectively target and modulate the activity of Gas7. These inhibitors serve as indispensable tools in laboratory investigations, enabling researchers to delve into the intricate molecular functions and cellular processes associated with Gas7.
Gas7 inhibitors typically function by interfering with the interactions or functions of Gas7 with cytoskeletal elements, membrane components, or other cellular proteins, thereby affecting its role in cell morphology, actin filament dynamics, and cellular signaling. This interference can lead to alterations in cellular shape, cytoskeletal organization, and signaling cascades, potentially impacting various aspects of cell behavior and function. Researchers employ Gas7 inhibitors to gain insights into the physiological roles and molecular interactions of Gas7 within cells, aiming to advance our understanding of the fundamental mechanisms involved in cytoskeletal dynamics, membrane remodeling, and intracellular signaling pathways. Through the study of Gas7 inhibitors, scientists seek to unravel the complexities of cellular architecture, structural plasticity, and the broader field of cell biology, contributing to our knowledge of how cells maintain their shape and respond to environmental cues.
Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
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Actinomycin D | 50-76-0 | sc-200906 sc-200906A sc-200906B sc-200906C sc-200906D | 5 mg 25 mg 100 mg 1 g 10 g | $73.00 $238.00 $717.00 $2522.00 $21420.00 | 53 | |
Actinomycin D intercalates into DNA, inhibiting transcription and potentially decreasing Gas7 expression across cell types. | ||||||
Cycloheximide | 66-81-9 | sc-3508B sc-3508 sc-3508A | 100 mg 1 g 5 g | $40.00 $82.00 $256.00 | 127 | |
Cycloheximide inhibits protein synthesis by interfering with the translocation step in protein synthesis, potentially reducing Gas7 levels. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin inhibits mTOR, a pathway that can regulate protein synthesis and potentially lower Gas7 expression. | ||||||
5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
A cytidine analog that inhibits DNA methyltransferase, potentially affecting Gas7 gene expression through epigenetic modifications. | ||||||
Trichostatin A | 58880-19-6 | sc-3511 sc-3511A sc-3511B sc-3511C sc-3511D | 1 mg 5 mg 10 mg 25 mg 50 mg | $149.00 $470.00 $620.00 $1199.00 $2090.00 | 33 | |
Trichostatin A is a histone deacetylase inhibitor, which can alter chromatin structure and potentially downregulate Gas7 expression. | ||||||
Retinoic Acid, all trans | 302-79-4 | sc-200898 sc-200898A sc-200898B sc-200898C | 500 mg 5 g 10 g 100 g | $65.00 $319.00 $575.00 $998.00 | 28 | |
Retinoic acid modulates gene expression and differentiation and could decrease Gas7 expression in certain differentiation contexts. | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
As a glucocorticoid, dexamethasone can regulate gene expression and may suppress Gas7 expression in some cell types. | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Mithramycin A binds to G-C rich DNA sequences and inhibits Sp1 transcription factor, potentially reducing Gas7 expression. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $226.00 $846.00 | 1 | |
JQ1 inhibits BET bromodomain proteins, which may downregulate Gas7 expression by altering chromatin accessibility. | ||||||
GSK-3 Inhibitor XVI | 252917-06-9 | sc-221691 sc-221691A | 5 mg 25 mg | $153.00 $520.00 | 4 | |
CHIR99021 is a GSK-3β inhibitor and could lead to altered Wnt signaling and subsequent downregulation of Gas7. |