FAM128A, also known as mitotic spindle organizing protein 2A (MZT2A), plays a critical role in the proper formation and function of the mitotic spindle during cell division. This protein is part of the MOZART (Mitotic-spindle Organizing protein associated with a Ring of γ-Tubulin complex) family, which is integral to the process of spindle assembly and thus to the accurate segregation of chromosomes in mitosis. FAM128A's ubiquitous expression across a variety of human tissues, including the prostate and colon, underscores its fundamental role in cellular proliferation and maintenance. The gene encoding FAM128A is located on the human chromosome and has been studied in the context of its cellular localization to the centrosome, cytosol, and nucleoplasm.
The expression of FAM128A, like many genes involved in cell cycle regulation, can potentially be induced by a variety of chemical compounds that affect cellular microtubule dynamics and DNA integrity. For instance, chemicals that disrupt microtubule polymerization, such as Nocodazole, could potentially lead to an upsurge in FAM128A expression as the cell mobilizes a response to stabilize spindle fibers and ensure accurate chromosomal alignment and segregation. Similarly, DNA-damaging agents such as Doxorubicin, which intercalates into DNA and interrupts replication and transcription processes, may prompt a cellular defensive strategy that includes the upregulation of proteins like FAM128A, which are involved in the structural integrity of mitotic spindles. Compounds such as Etoposide, which induces DNA strand breaks through inhibition of topoisomerase II, could conceivably stimulate a heightened expression of FAM128A in an attempt to bolster the cell's apparatus for chromosomal management during the critical phases of cell division. Furthermore, as cells encounter agents like Paclitaxel, a stabilizer of microtubules, the cellular feedback mechanisms may include the induction of spindle organizing proteins including FAM128A to maintain the equilibrium of spindle dynamics. Each of these chemical interactions with cellular processes serves to illustrate the complex network of cellular surveillance and response systems that govern gene expression regulation, particularly for genes as pivotal as FAM128A.
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| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
Doxorubicin | 23214-92-8 | sc-280681 sc-280681A | 1 mg 5 mg | $176.00 $426.00 | 43 | |
Doxorubicin may upregulate FAM128A by inducing DNA damage response pathways, which can lead to an increased expression of genes associated with cell cycle checkpoints and mitotic spindle organization. | ||||||
Taxol | 33069-62-4 | sc-201439D sc-201439 sc-201439A sc-201439E sc-201439B sc-201439C | 1 mg 5 mg 25 mg 100 mg 250 mg 1 g | $41.00 $74.00 $221.00 $247.00 $738.00 $1220.00 | 39 | |
By stabilizing microtubules, Taxol could stimulate the expression of FAM128A as a response to altered microtubule dynamics and to support proper spindle assembly during mitosis. | ||||||
Vinblastine | 865-21-4 | sc-491749 sc-491749A sc-491749B sc-491749C sc-491749D | 10 mg 50 mg 100 mg 500 mg 1 g | $102.00 $235.00 $459.00 $1749.00 $2958.00 | 4 | |
Vinblastine may increase FAM128A expression by disrupting microtubule assembly, triggering compensatory mechanisms that upregulate proteins essential for mitotic spindle function. | ||||||
Fluorouracil | 51-21-8 | sc-29060 sc-29060A | 1 g 5 g | $37.00 $152.00 | 11 | |
This antimetabolite may stimulate the transcription of FAM128A as part of a cellular response to thymidylate synthase inhibition, which is critical for DNA synthesis and cell division. | ||||||
Nocodazole | 31430-18-9 | sc-3518B sc-3518 sc-3518C sc-3518A | 5 mg 10 mg 25 mg 50 mg | $59.00 $85.00 $143.00 $247.00 | 38 | |
Nocodazole could induce the expression of FAM128A by interfering with microtubule polymerization, thereby activating pathways that compensate for spindle assembly disruption. | ||||||
Bleomycin | 11056-06-7 | sc-507293 | 5 mg | $275.00 | 5 | |
As a DNA damaging agent, Bleomycin could lead to an upregulation of FAM128A due to the activation of DNA repair mechanisms and checkpoint controls in cell cycle progression. | ||||||
Etoposide (VP-16) | 33419-42-0 | sc-3512B sc-3512 sc-3512A | 10 mg 100 mg 500 mg | $51.00 $231.00 $523.00 | 63 | |
Etoposide may increase FAM128A levels by causing DNA strand breaks, subsequently initiating a cellular response that requires enhanced mitotic spindle organization for DNA damage repair. | ||||||
Camptothecin | 7689-03-4 | sc-200871 sc-200871A sc-200871B | 50 mg 250 mg 100 mg | $58.00 $186.00 $94.00 | 21 | |
Camptothecin could stimulate FAM128A expression due to its role as a topoisomerase I inhibitor, necessitating an upregulation of proteins that maintain genomic stability during cell division. | ||||||
Methotrexate | 59-05-2 | sc-3507 sc-3507A | 100 mg 500 mg | $94.00 $213.00 | 33 | |
Methotrexate may induce FAM128A transcription as a response to folate pathway inhibition, affecting DNA synthesis and repair, processes requiring proper spindle formation. | ||||||
Hydroxyurea | 127-07-1 | sc-29061 sc-29061A | 5 g 25 g | $78.00 $260.00 | 18 | |
By inhibiting ribonucleotide reductase, Hydroxyurea may stimulate FAM128A expression to support DNA damage repair and ensure accurate chromosomal segregation. | ||||||