Formin 2 Polyclonal Antibody, 20ul Aspirating Pipets Upgrade today

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Defects in this gene are a cause of juvenile-onset pulverulent cataract as well as congenital cerulean cataract 4 (CCA4)

Forkhead box protein R1 lacks the C-terminal basic region found in many other FOX family members

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The protein encoded by CD3E (CD3e molecule) is the CD3-epsilon polypeptide

Formin 2 Polyclonal Antibody, 20ul Aspirating Pipets Upgrade todayFMN2 (formin 2) is a member of the formin homology protein family. The encoded protein is thought to have essential roles in organization of the actin cytoskeleton and in cell polarity. Mutations in FMN2 have been associated with mental retardation autosomal recessive 47 (MRT47). Alternatively spliced transcript variants have been identified.