LIN41 Polyclonal Antibody, 100ul Gene Editing Mutations in ATRX are associated

Mutations in ATRX are associated with an X-linked mental retardation (XLMR) syndrome most often accompanied by alpha-thalassemia (ATRX) syndrome

oxidatives stress and anisomycin treatments

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which causes reduced sclerostin expression

Expression of this gene may be regulated by the cytokine TNF-alpha

LIN41 Polyclonal Antibody, 100ul Gene Editing Mutations in ATRX are associatedThe protein encoded by this gene is an E3 ubiquitin protein ligase that binds with miRNAs and maintains the growth and upkeep of embryonic stem cells. This gene also is involved in the G1 S phase transition of the cell cycle.