|Application ||WB, E|
|Other Accession||Q9JJG5, NP_055570.1|
|Calculated MW||33897 Da|
|Antigen Region||1-30 aa|
|Other Names||SERTA domain-containing protein 2, Transcriptional regulator interacting with the PHD-bromodomain 2, TRIP-Br2, SERTAD2, KIAA0127|
|Target/Specificity||This SERTAD2 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human SERTAD2.|
|Format||Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.|
|Storage||Maintain refrigerated at 2-8°C for up to 2 weeks. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.|
|Precautions||SERTAD2 Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.|
|Function||Acts at E2F-responsive promoters as coregulator to integrate signals provided by PHD- and/or bromodomain-containing transcription factors. May act as coactivator as well as corepressor of E2F1-TFDP1 and E2F4-TFDP1 complexes on E2F consensus binding sites, which would activate or inhibit E2F- target genes expression. Modulates fat storage by down-regulating the expression of key genes involved in adipocyte lipolysis, thermogenesis and oxidative metabolism.|
|Cellular Location||Nucleus. Cytoplasm. Note=Exported out of the nucleus via its NES in a XPO1-dependent manner. Once in the cytoplasm, is degraded by the proteasome|
|Tissue Location||Expressed in adipose tissue.|
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Provided below are standard protocols that you may find useful for product applications.
SERTAD2 acts at E2F-responsive promoters to integrate signals provided by PHD-and/or bromodomain-containing transcription factors (By similarity).
Rose, J. Phd, et al. Mol. Med. (2010) In press :
Cheong, J.K., et al. J Transl Med 7, 8 (2009) :
Cheong, J.K., et al. J. Biol. Chem. 283(17):11661-11676(2008)
Watanabe-Fukunaga, R., et al. Genes Cells 10(8):851-860(2005)
Hillier, L.W., et al. Nature 434(7034):724-731(2005)
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