Date published: 2025-10-15

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Mi2-α Activators

Mi2-α activators represent a set of chemicals that influence the activity of the Mi2-α protein, albeit most of them indirectly. This protein is an integral part of the NuRD complex, which plays pivotal roles in chromatin remodeling-a process vital for transcription, DNA repair, and replication. Chromatin's dynamic nature relies on post-translational modifications, such as acetylation and methylation, which control the accessibility of DNA to the transcriptional machinery.

Among the listed chemicals, many, like Trichostatin A, Valproic Acid, Vorinostat, and Sodium Butyrate, are HDAC inhibitors. These inhibitors increase histone acetylation, leading to a more relaxed chromatin structure, thereby influencing Mi2-α's function. On the other hand, 5-Azacytidine and RG108 are DNMT inhibitors, targeting the DNA methylation machinery and indirectly impacting chromatin remodeling. In a similar vein, BIX-01294, EPZ-6438, and UNC1999 target the histone methylation machinery. JQ1, a BET bromodomain inhibitor, adds another layer to the intricate interplay of chromatin modifiers by influencing gene transcription. All these chemicals converge on the central theme of chromatin modifications, highlighting the complexity of the network in which Mi2-α operates.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

DNMT inhibitor, altering methylation of DNA and possibly influencing gene expression linked to Mi2-α.

Mocetinostat

726169-73-9sc-364539
sc-364539B
sc-364539A
5 mg
10 mg
50 mg
$210.00
$242.00
$1434.00
2
(1)

HDAC inhibitor, affects chromatin remodeling indirectly possibly influencing Mi2-α.

(±)-JQ1

1268524-69-1sc-472932
sc-472932A
5 mg
25 mg
$226.00
$846.00
1
(0)

BET bromodomain inhibitor, influences gene transcription and potentially Mi2-α.