Menin Polyclonal Antibody, 20ul sgRNA Oligos Defects in this gene are

Defects in this gene are a cause of branchiooculofacial syndrome (BOFS)

Allelic variations in this gene have been associated with atopy

Localizing to cytoplasm

Annexin VII encodes a protein with a molecular weight of approximately 51 kDa with a unique

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Menin Polyclonal Antibody, 20ul sgRNA Oligos Defects in this gene areMEN1 encodes menin, a putative tumor suppressor associated with a syndrome known as multiple endocrine neoplasia type 1. In vitro studies have shown menin is localized to the nucleus, possesses two functional nuclear localization signals, and inhibits transcriptional activation by JunD, however, the function of this protein is not known. Two messages have been detected on northern blots but the larger message has not been characterized. Alternative