ZNF670 activators constitute a specialized category of chemical compounds that have captured the attention of researchers within the field of molecular biology and genetics. These compounds are meticulously designed to modulate the activity of ZNF670, a protein-coding gene that plays a role in a diverse array of cellular processes. ZNF670, short for Zinc Finger Protein 670, belongs to the zinc finger transcription factor family, characterized by its ability to bind to specific DNA sequences, thereby influencing gene expression. ZNF670 activators operate by interacting with distinct regulatory elements affiliated with the ZNF670 gene, typically located within promoter or enhancer regions, with the overarching goal of facilitating its transcription and subsequent translation into functional protein products.
The precise mechanisms through which ZNF670 activators exert their effects can vary, but their fundamental objective is to act as molecular switches, amplifying the activity of ZNF670. Researchers are continually delving into the potential applications and implications of ZNF670 activation, as they endeavor to decipher the intricate roles this gene fulfills in numerous cellular processes. This class of compounds holds promise for advancing our comprehension of gene regulation, particularly within the context of the zinc finger transcription factor family, offering insights into their importance in cellular development and the control of gene expression. ZNF670 activators thus serve as valuable tools in the ongoing exploration of molecular biology, helping to elucidate the complex mechanisms that underpin gene regulation and cellular functions.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Isoproterenol Hydrochloride | 51-30-9 | sc-202188 sc-202188A | 100 mg 500 mg | $27.00 $37.00 | 5 | |
As a beta-adrenergic agonist, Isoproterenol can increase intracellular cAMP, potentially activating CREB and influencing ZNF670 expression. | ||||||
Staurosporine | 62996-74-1 | sc-3510 sc-3510A sc-3510B | 100 µg 1 mg 5 mg | $82.00 $150.00 $388.00 | 113 | |
Staurosporine is a potent protein kinase inhibitor, which could affect multiple signaling pathways, potentially altering ZNF670 expression. | ||||||
Tamoxifen | 10540-29-1 | sc-208414 | 2.5 g | $256.00 | 18 | |
As a selective estrogen receptor modulator, Tamoxifen can influence estrogen-responsive gene expression, potentially including ZNF670. | ||||||
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, affecting cellular growth and metabolism pathways, potentially leading to changes in ZNF670 expression. | ||||||
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 | |
Curcumin can modulate various signaling pathways, including NF-κB, potentially affecting the transcription of genes like ZNF670. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $32.00 $170.00 $385.00 | 63 | |
Etoposide induces DNA damage response, which can activate p53 and potentially influence the expression of p53-regulated genes, including ZNF670. | ||||||
Tunicamycin | 11089-65-9 | sc-3506A sc-3506 | 5 mg 10 mg | $169.00 $299.00 | 66 | |
Tunicamycin induces ER stress by inhibiting N-linked glycosylation, potentially affecting the expression of stress-responsive genes like ZNF670. | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
Chloroquine inhibits autophagy by disrupting lysosome acidification, potentially affecting cellular stress responses and ZNF670 expression. | ||||||
(±)-JQ1 | 1268524-69-1 | sc-472932 sc-472932A | 5 mg 25 mg | $226.00 $846.00 | 1 | |
JQ1 inhibits BET bromodomains, potentially affecting chromatin accessibility and the expression of genes like ZNF670. | ||||||
Y-27632, free base | 146986-50-7 | sc-3536 sc-3536A | 5 mg 50 mg | $182.00 $693.00 | 88 | |
Y-27632 is a ROCK inhibitor, potentially affecting cytoskeleton organization and signaling, which could influence ZNF670 expression. | ||||||