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Is important for morphogenesis of limb and kidney and may be involved in determining dorsoventral neural tube polarity and motor neuron induction. Additionally we are shipping FMN1 Antibodies (22) and FMN1 Proteins (4) and many more products for this protein.
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Filopodia initiation: focus on the Arp2 (show ACTR2 ELISA Kits)/3 complex and formins.
Chromosomal imbalances in the GREM1 (show GREM1 ELISA Kits) FMN1 region in individuals with limb defects are reported here.
The obtained data indicate the possibility of participation of polymorphism in gene FMN1 in formation of predisposition to prostate cancer.
both mammalian Spir proteins, Spir-1 (show SPIRE1 ELISA Kits) and Spir-2 (show SPIRE1 ELISA Kits), interact with mammalian Fmn subgroup proteins formin-1 and formin-2 (show FMN2 ELISA Kits)
Fmn1 and FlnB (show FLNB ELISA Kits) have shared and independent functions.
Results suggest that the regulation of microtubule acetylation is likely a general formin activity.
These results reveal a previously unknown involvement of Formin1 in dendritogenesis and synaptogenesis and indicate that this protein is a key component of the Ngn3 (show NEUROG3 ELISA Kits) signaling pathway that controls neuronal differentiation.
the mouse formin, FRLalpha, slows actin filament barbed end elongation, competes with capping protein, accelerates polymerization from monomers, and severs filaments
ATP hydrolysis control of filament assembly from profilin (show PFN1 ELISA Kits)-actin requires formin
It was determined that Fmn1-IV, as an actin nucleator, contributes to protrusion of the cell's leading edge and focal adhesion formation, thus contributing to cell motility
Disruption of Fmn1 gene in mice increased Bmp signaling.
Is important for morphogenesis of limb and kidney and may be involved in determining dorsoventral neural tube polarity and motor neuron induction. It may also have a function in differentiated cells or be involved in maintaining specific differentiated states.
, formin (limb deformity)
, limb deformity protein homolog
, limb deformity protein