Synthetic peptide. This information is considered to be commercially sensitive.
Conjugation:
Unconjugated
Alternative Names:
TSGA, JMJD1, JHDM2A, JHMD2A, JMJD1A, KDM3A
Enables androgen receptor binding activity, histone H3-methyl-lysine-9 demethylase activity, and iron ion binding activity. Involved in several processes, including androgen receptor signaling pathway, formaldehyde biosynthetic process, and histone H3-K9 demethylation. Located in nucleoplasm. Implicated in cervical cancer and colon cancer. Biomarker of Ewing sarcoma, hepatocellular carcinoma, nasopharynx carcinoma, and prostate cancer.
WB,1:500 - 1:1000|IHC-P,1:50 - 1:200|IF/ICC,1:50 - 1:200|ELISA,Recommended starting concentration is 1 µg/mL. Please optimize the concentration based on your specific assay requirements.
Application Notes:
Cross-Reactivity: Human, ResearchArea: Epigenetics Nuclear Signaling,Epigenetic writers and erasers of core Histones.
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