The chemical class known as LOC100041407 Activators, also referred to by the designation predicted pseudogene 3320 activators, encompasses a series of compounds that are specifically formulated to target and influence the activity of the LOC100041407 sequence, classified within the realm of pseudogenes. Pseudogenes, traditionally considered as non-functional remnants of gene duplication or gene decay, have been increasingly recognized for their potential regulatory roles in gene expression and genomic architecture. The activators within this class are characterized by their capability to interact with the LOC100041407 sequence, potentially impacting its regulatory functions, which may include acting as decoys for transcription factors, influencing the stability of mRNAs, or modulating the chromatin environment to affect the expression of nearby genes. The interaction mechanism between these activators and LOC100041407 involves complex molecular dynamics, potentially encompassing interactions with regulatory RNA molecules, alterations in the local chromatin structure, or indirect effects on gene regulation through the modulation of transcriptional networks.
Delving into the functionality and implications of LOC100041407 activators requires an expansive understanding of the nuanced roles that pseudogenes play within the cellular and genetic landscape. Despite their initial classification as 'junk' DNA, pseudogenes like LOC100041407 are now considered to be integral components of the genomic regulatory network, with the capacity to influence gene expression and cellular processes subtly. By modulating the activity of LOC100041407, these activators can shed light on the intricate mechanisms through which pseudogenes contribute to cellular homeostasis, gene regulation, and the complex interplay between various elements of the genome. This exploration not only enhances our understanding of the genetic and epigenetic factors that govern cellular function but also opens new avenues for investigating the broader implications of non-coding DNA in the regulation of gene expression and the maintenance of genomic integrity.
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产品名称 | CAS # | 产品编号 | 数量 | 价格 | 应用 | 排名 |
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5-Azacytidine | 320-67-2 | sc-221003 | 500 mg | $280.00 | 4 | |
5-Azacytidine 是 DNA 甲基转移酶的抑制剂,可导致沉默基因的去甲基化和可能的表达。 | ||||||
Suberoylanilide Hydroxamic Acid | 149647-78-9 | sc-220139 sc-220139A | 100 mg 500 mg | $130.00 $270.00 | 37 | |
伏立诺他是一种 HDAC 抑制剂,可使染色质状态更加开放,并有可能转录通常沉默的基因组区域。 | ||||||
5-Aza-2′-Deoxycytidine | 2353-33-5 | sc-202424 sc-202424A sc-202424B | 25 mg 100 mg 250 mg | $214.00 $316.00 $418.00 | 7 | |
与 5-氮杂胞苷类似,地西他滨也可导致 DNA 去甲基化,可能会影响假基因的转录。 | ||||||
Disulfiram | 97-77-8 | sc-205654 sc-205654A | 50 g 100 g | $52.00 $87.00 | 7 | |
作为醛脱氢酶的抑制剂,双硫仑可改变组蛋白的乙酰化状态,从而可能影响基因表达。 | ||||||
Valproic Acid | 99-66-1 | sc-213144 | 10 g | $85.00 | 9 | |
丙戊酸是另一种HDAC抑制剂,可通过改变染色质结构来改变基因表达。 | ||||||
Mithramycin A | 18378-89-7 | sc-200909 | 1 mg | $54.00 | 6 | |
Mithramycin A 与富含 GC 的 DNA 序列结合,可影响某些基因的转录物。 | ||||||
Ademetionine | 29908-03-0 | sc-278677 sc-278677A | 100 mg 1 g | $180.00 $655.00 | 2 | |
S-Adenosylmethionine 是甲基转移反应的甲基供体,可间接影响基因表达模式。 | ||||||
Vitamin A | 68-26-8 | sc-280187 sc-280187A | 1 g 10 g | $377.00 $2602.00 | ||
视黄醇及其衍生物通过视黄酸受体影响基因表达,从而影响细胞分化和基因转录。 | ||||||
Dexamethasone | 50-02-2 | sc-29059 sc-29059B sc-29059A | 100 mg 1 g 5 g | $76.00 $82.00 $367.00 | 36 | |
地塞米松是一种糖皮质激素受体激动剂,可通过受体转录因子的活性调节基因表达。 | ||||||
Chloroquine | 54-05-7 | sc-507304 | 250 mg | $68.00 | 2 | |
氯喹会影响溶酶体酸度,影响表观遗传调控和 DNA 修复机制,从而可能影响基因表达。 |