SEPT9 Polyclonal Antibody, 100ul Oligo Pool remodelling of membrane lipids

remodelling of membrane lipids

The encoded protein contains two EF-hand Ca2+ binding domains in its N-terminus and two glutamine- and threonine-rich 60 amino acid repeats in its C-terminus

Mutations in this gene have been associated with congenital myasthenic syndrome

and abnormal chromosome segregation

but is limited in neural organs in normal tissues

SEPT9 Polyclonal Antibody, 100ul Oligo Pool remodelling of membrane lipidsThis gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript