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INF2 represents a member of the formin family of proteins. Additionally we are shipping INF2 Proteins (6) and INF2 Kits (2) and many more products for this protein.
Showing 10 out of 43 products:
Human Polyclonal INF2 Primary Antibody for ICC, IF - ABIN4325815
Sun, Al-Romaih, MacRae, Pollak: Human Kidney Disease-causing INF2 Mutations Perturb Rho/Dia Signaling in the Glomerulus. in EBioMedicine 2015
The authors propose Spire1C isoform cooperates with INF2 to regulate actin assembly at endoplasmic reticulum-mitochondrial contacts.
Report novel mutations in the inverted formin 2 gene of Chinese families contributing to focal segmental glomerulosclerosis.
Assembly and turnover of short actin filaments by the formin (show FMN1 Antibodies) INF2 and profilin (show PFN1 Antibodies).
INF2 mutations are associated with focal segmental glomerulosclerosis.
this study identifed three novel mutations of INF (show GIF Antibodies) likely efect hereditary neuropathy with glomerulopathy.
actin monomer binding to the DAD of INF2 competes with the DID/DAD interaction, thereby activating actin polymerization
INF2 mutation was detected both father and his son
This study showed that INF2 mutations in Charcot-Marie-Tooth disease complicated with focal segmental glomerulosclerosis.
In podocytes, INF2 appears to be an important modulator of actin-dependent behaviors that are under the control of Rho/mDia signaling.
INF2 mutations were found in 2 of 281 individuals with sporadicfocal and segmental glomerulosclerosis
The perinuclear actin rim (show RIMS1 Antibodies) structure colocalized with INF2 on stimulation, and INF2 depletion resulted in attenuation of the rim (show RIMS1 Antibodies) formation.
INF2 plays a role in controlling morphological, but not compositional maturation of focal adhesions
Splice variant-specific cellular function of the formin (show FMN1 Antibodies) INF2 in maintenance of Golgi architecture.
Data suggest a role for INF1 in microtubule modification and potentially in coordinating microtubule and F-actin structure.
This gene represents a member of the formin family of proteins. It is considered a diaphanous formin due to the presence of a diaphanous inhibitory domain located at the N-terminus of the encoded protein. Studies of a similar mouse protein indicate that the protein encoded by this locus may function in polymerization and depolymerization of actin filaments. Mutations at this locus have been associated with focal segmental glomerulosclerosis 5.
HBEAG-binding protein 2 binding protein C
, HBEBP2-binding protein C
, inverted formin-2
, formin, inverted