USF1 Polyclonal Antibody, 100ul Cell Culture Flasks Loss of sequences from human

Loss of sequences from human chromosome 10q has been associated with the progression of human cancers

such as NALP2

|tissue specificity:Expressed in brain| lung| heart| skeletal muscle| kidney| liver and placenta

This receptor is also an essential mediator for osteoclast and lymph node development

It may be downstream in the WNT1 signaling pathway that is relevant to malignant transformation

USF1 Polyclonal Antibody, 100ul Cell Culture Flasks Loss of sequences from humanThis gene encodes a member of the basic helix loop helix leucine zipper family, and can function as a cellular transcription factor. The encoded protein can activate transcription through pyrimidine rich initiator (Inr) elements and E box motifs. This gene has been linked to familial combined hyperlipidemia (FCHL). Alternative splicing of this gene results in multiple transcript variants. A related pseudogene has been defined on chromosome 21.