OTTMUSG00000010441 Inhibitors
OTTMUSG00000010441 inhibitors are a class of chemical compounds designed to selectively target and inhibit the function of the protein encoded by the gene OTTMUSG00000010441, based on mouse genomic data. Although the exact role of this gene product may not be fully established, proteins encoded by genes like OTTMUSG00000010441 typically participate in essential cellular processes such as signal transduction, gene regulation, or cellular structural maintenance. The inhibitors work by disrupting the normal activity of the protein, potentially through mechanisms such as blocking its ability to bind to specific molecular partners, interfering with enzymatic actions, or preventing its role in intracellular signaling pathways. By inhibiting OTTMUSG00000010441, researchers can investigate the downstream effects on cellular processes that rely on its proper function.
The use of OTTMUSG00000010441 inhibitors provides a powerful tool for studying the specific biological functions of this gene and its encoded protein within the cell. When its function is blocked, researchers can observe changes in cellular behaviors such as gene expression modulation, metabolic regulation, or protein-protein interactions. This helps to elucidate how OTTMUSG00000010441 integrates into broader cellular networks and how its activity influences key molecular pathways. Additionally, these inhibitors allow scientists to explore how the loss of function impacts cellular homeostasis and stability, providing insights into the intricate regulatory mechanisms that govern essential cellular processes. Through these studies, OTTMUSG00000010441 inhibitors help clarify the role of this protein in the molecular landscape of the cell, contributing to a more detailed understanding of gene-driven cellular regulation.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Ophiobolin A | 4611-05-6 | sc-202266 sc-202266A sc-202266B | 100 µg 1 mg 5 mg | $43.00 $245.00 $714.00 | 7 | |
Ophiobolin A, a sesterterpene produced by fungi, is a potent inhibitor of calmodulin, a protein known to interact with various cellular signaling pathways including those involved in cell cycle regulation and apoptosis. By inhibiting calmodulin, Ophiobolin A can indirectly inhibit pramel family members involved in these pathways by disrupting their regulatory mechanisms. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
PD 98059 is a selective inhibitor of MEK, a key kinase in the MAPK/ERK pathway, which is often involved in cell proliferation and differentiation processes. Since pramel family members might be implicated in similar cellular processes, inhibiting MEK could indirectly disrupt pramel family member's functional pathways, leading to inhibition. | ||||||
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002 is a potent inhibitor of PI3K, a kinase involved in the AKT signaling pathway. This pathway is crucial for many cellular processes including cell survival and growth. By inhibiting PI3K, LY294002 could indirectly inhibit pramel family member functions related to these processes. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
Rapamycin is a specific inhibitor of mTOR, a central regulator of cell growth and proliferation. Since pramel family members could be involved in cellular growth processes, inhibiting mTOR with Rapamycin might indirectly inhibit the functional role of pramel family members. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
U0126 is an inhibitor of MEK1/2, key components of the MAPK/ERK pathway. This pathway is involved in cell cycle regulation and differentiation, processes potentially influenced by pramel family members. Inhibiting MEK1/2 could therefore indirectly inhibit the functions of pramel family members. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
SB203580 is a specific inhibitor of p38 MAP kinase, a protein involved in response to stress and inflammatory cytokines. As pramel family members might be implicated in these responses, inhibiting p38 MAP kinase could indirectly inhibit their function. | ||||||
SP600125 | 129-56-6 | sc-200635 sc-200635A | 10 mg 50 mg | $65.00 $267.00 | 257 | |
SP600125 is an inhibitor of JNK, a kinase involved in stress response, apoptosis, and cell differentiation. These processes might be regulated by pramel family members, so inhibiting JNK could lead to indirect inhibition of their function. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
Wortmannin is a potent inhibitor of PI3K. Since PI3K/AKT pathway is crucial in cell survival and proliferation, and potentially in processes regulated by pramel family members, inhibiting this pathway with Wortmannin could indirectly inhibit pramel family member functions. | ||||||
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. By altering chromatin structure and gene expression, it can indirectly influence cellular processes including those regulated by pramel family members, thereby potentially inhibiting their function. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
Bortezomib, a proteasome inhibitor, impacts protein degradation pathways. Since protein turnover is crucial for various cellular processes, inhibiting proteasome activity with Bortezomib might indirectly affect the functional role of pramel family members. | ||||||