This is a Validated Antibody Database (VAD) review about human FLNC, based on 6 published articles (read how Labome selects the articles), using FLNC antibody in all methods. It is aimed to help Labome visitors find the most suited FLNC antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
FLNC synonym: ABP-280; ABP280A; ABPA; ABPL; CMH26; FLN2; MFM5; MPD4; RCM5; filamin-C; ABP-280-like protein; ABP-L, gamma filamin; actin binding protein 280; filamin C, gamma; filamin-2; gamma filamin

Sigma-Aldrich
rabbit polyclonal
  • immunohistochemistry - paraffin section; human; loading ...; fig 3a
Sigma-Aldrich FLNC antibody (Sigma-Aldrich, HPA006135) was used in immunohistochemistry - paraffin section on human samples (fig 3a). Circ Cardiovasc Genet (2017) ncbi
rabbit polyclonal
  • immunohistochemistry - frozen section; mouse; 1:500; loading ...; fig 6c
Sigma-Aldrich FLNC antibody (Sigma-Aldrich, HPA006135) was used in immunohistochemistry - frozen section on mouse samples at 1:500 (fig 6c). J Clin Invest (2017) ncbi
rabbit polyclonal
  • immunohistochemistry - frozen section; human; loading ...; fig 4h
Sigma-Aldrich FLNC antibody (Sigma-Aldrich, HPA006135) was used in immunohistochemistry - frozen section on human samples (fig 4h). J Clin Endocrinol Metab (2017) ncbi
rabbit polyclonal
  • western blot; mouse; fig 4
In order to investigate the modulator of skeletal muscle sarcomeric morphometry associated to modulation of protein-protein interactions by O-GlcNAcylation, Sigma-Aldrich FLNC antibody (Sigma, HPA006135) was used in western blot on mouse samples (fig 4). Biochim Biophys Acta (2016) ncbi
rabbit polyclonal
Sigma-Aldrich FLNC antibody (Sigma, HPA006135) was used . Hypertension (2015) ncbi
rabbit polyclonal
Sigma-Aldrich FLNC antibody (Sigma, HPA006135) was used . Neuromuscul Disord (2015) ncbi
Articles Reviewed
  1. Tucker N, McLellan M, Hu D, Ye J, Parsons V, Mills R, et al. Novel Mutation in FLNC (Filamin C) Causes Familial Restrictive Cardiomyopathy. Circ Cardiovasc Genet. 2017;10: pubmed publisher
  2. Papizan J, Garry G, Brezprozvannaya S, McAnally J, Bassel Duby R, Liu N, et al. Deficiency in Kelch protein Klhl31 causes congenital myopathy in mice. J Clin Invest. 2017;127:3730-3740 pubmed publisher
  3. Krag T, Ruiz Ruiz C, Vissing J. Glycogen Synthesis in Glycogenin 1-Deficient Patients: A Role for Glycogenin 2 in Muscle. J Clin Endocrinol Metab. 2017;102:2690-2700 pubmed publisher
  4. Lambert M, Richard E, Duban Deweer S, Krzewinski F, Deracinois B, Dupont E, et al. O-GlcNAcylation is a key modulator of skeletal muscle sarcomeric morphometry associated to modulation of protein-protein interactions. Biochim Biophys Acta. 2016;1860:2017-30 pubmed publisher
  5. Zhou J, Shaikh L, Neogi S, McFarlane I, Zhao W, Figg N, et al. DACH1, a zona glomerulosa selective gene in the human adrenal, activates transforming growth factor-β signaling and suppresses aldosterone secretion. Hypertension. 2015;65:1103-10 pubmed publisher
  6. Barresi R, Morris C, Hudson J, Curtis E, Pickthall C, Bushby K, et al. Conserved expression of truncated telethonin in a patient with limb-girdle muscular dystrophy 2G. Neuromuscul Disord. 2015;25:349-52 pubmed publisher