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- Table of Contents
Designing a Western blot for Inverted formin-2? The guide has the expected band size, antibodies backed by real blot images, the controls to run alongside, and protocols taken from published papers.
Open the INF2 Western Blot GuideDesigning an IHC experiment for Inverted formin-2? The guide has the expected staining pattern, antigen retrieval and fixation, antibodies backed by real IHC images, the tissue controls to run alongside, and protocols taken from published papers.
Open the INF2 IHC GuideFacts about Inverted formin-2.
.
| Human | |
|---|---|
| Gene Name: | INF2 |
| Uniprot: | Q27J81 |
| Entrez: | 64423 |

| Belongs to: |
|---|
| formin homology family |

C14orf151; C14orf173DKFZp762A0214; chromosome 14 open reading frame 151; chromosome 14 open reading frame 173; FLJ22056; FSGS5; HBEAG-binding protein 2 binding protein C; HBEBP2-binding protein C; inverted formin, FH2 and WH2 domain containing; inverted formin-2; MGC13251; pp9484
Mass (kDA):
135.624 kDA

| Human | |
|---|---|
| Location: | 14q32.33 |
| Sequence: | 14; NC_000014.9 (104689606..104722535) |
Widely expressed. In the kidney, expression is apparent in podocytes and some tubule cells.
Cytoplasm, perinuclear region.




PMID: 20023659 by Brown E.J., et al. Mutations in the formin gene INF2 cause focal segmental glomerulosclerosis.
PMID: 21258034 by Boyer O., et al. Mutations in INF2 are a major cause of autosomal dominant focal segmental glomerulosclerosis.