OTTMUSG00000010322 inhibitors are a class of chemical compounds specifically designed to target and inhibit the activity of the protein encoded by the gene OTTMUSG00000010322, identified from mouse genomic data. Although the specific function of this gene may not be fully characterized, proteins encoded by similar genes are often involved in critical cellular processes, including signaling pathways, gene expression regulation, or structural roles within the cell. The inhibition of OTTMUSG00000010322 disrupts its normal function, potentially blocking interactions with other cellular molecules, preventing its involvement in catalysis, or interfering with downstream signaling processes. By inhibiting this protein, researchers can gain insight into the biological roles it plays, particularly how it contributes to maintaining cellular balance and regulating complex molecular networks.
Research into OTTMUSG00000010322 inhibitors provides valuable insights into the cellular and molecular mechanisms controlled by this protein. By blocking its function, scientists can study how inhibition affects various cellular processes such as intracellular signaling, protein interactions, and the regulation of cellular growth or differentiation. These inhibitors allow for a detailed examination of how the protein integrates with other pathways and how its disruption might influence broader cellular behavior. Furthermore, OTTMUSG00000010322 inhibitors serve as important tools for understanding the functional dynamics of gene-regulated systems and their role in ensuring cellular homeostasis. This research is critical for expanding our knowledge of molecular biology, particularly in areas involving protein interaction networks, signal transduction, and cellular regulation at the genetic level.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
LY 294002 | 154447-36-6 | sc-201426 sc-201426A | 5 mg 25 mg | $121.00 $392.00 | 148 | |
LY294002, a PI3K inhibitor, could alter Pramel function by modulating the PI3K/AKT pathway, affecting signal transduction processes that Pramel might be involved in. | ||||||
Rapamycin | 53123-88-9 | sc-3504 sc-3504A sc-3504B | 1 mg 5 mg 25 mg | $62.00 $155.00 $320.00 | 233 | |
As an mTOR inhibitor, Rapamycin potentially influences Pramel by affecting cell growth and proliferation pathways, which Pramel may regulate or be regulated by. | ||||||
PD 98059 | 167869-21-8 | sc-3532 sc-3532A | 1 mg 5 mg | $39.00 $90.00 | 212 | |
This MEK inhibitor could affect Pramel indirectly by altering the MAPK/ERK pathway, potentially impacting signaling processes associated with Pramel. | ||||||
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 | |
As an HDAC inhibitor, it might affect Pramel indirectly by changing chromatin structure and gene expression, which could be linked to Pramel's function. | ||||||
Bortezomib | 179324-69-7 | sc-217785 sc-217785A | 2.5 mg 25 mg | $132.00 $1064.00 | 115 | |
By inhibiting proteasome activity, Bortezomib could influence Pramel by affecting protein degradation processes that Pramel may be part of. | ||||||
U-0126 | 109511-58-2 | sc-222395 sc-222395A | 1 mg 5 mg | $63.00 $241.00 | 136 | |
This inhibitor of MEK in the MAPK/ERK pathway may indirectly influence Pramel by modulating cell signaling and proliferation. | ||||||
SB 203580 | 152121-47-6 | sc-3533 sc-3533A | 1 mg 5 mg | $88.00 $342.00 | 284 | |
A p38 MAPK inhibitor that could impact Pramel by modulating stress-related signaling pathways potentially relevant to its function. | ||||||
Curcumin | 458-37-7 | sc-200509 sc-200509A sc-200509B sc-200509C sc-200509D sc-200509F sc-200509E | 1 g 5 g 25 g 100 g 250 g 1 kg 2.5 kg | $36.00 $68.00 $107.00 $214.00 $234.00 $862.00 $1968.00 | 47 | |
This compound might affect Pramel indirectly through its anti-inflammatory properties, potentially impacting cellular signaling pathways. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Disrupting lysosomal function and autophagy, Chloroquine could indirectly affect Pramel's role in cellular processes by altering protein degradation. | ||||||
Wortmannin | 19545-26-7 | sc-3505 sc-3505A sc-3505B | 1 mg 5 mg 20 mg | $66.00 $219.00 $417.00 | 97 | |
As a PI3K inhibitor, Wortmannin could influence Pramel by altering signaling pathways that are critical to its function. | ||||||