This is a Validated Antibody Database (VAD) review about human FBN1, based on 3 published articles (read how Labome selects the articles), using FBN1 antibody in all methods. It is aimed to help Labome visitors find the most suited FBN1 antibody. Please note the number of articles fluctuates since newly identified citations are added and citations for discontinued catalog numbers are removed regularly.
FBN1 synonym: ACMICD; ECTOL1; FBN; GPHYSD2; MASS; MFLS; MFS1; OCTD; SGS; SSKS; WMS; WMS2

Invitrogen
mouse monoclonal (11C1.3)
  • immunocytochemistry; human; fig 1
In order to characterize arterial tortuosity syndrome skin fibroblasts and GLUT10 deficiency leading to non-canonical alpha-gamma-beta3 integrin-mediated TGF-beta singalling and oxidative stress with extracellular matrix disarray, Invitrogen FBN1 antibody (NeoMarkers, 11C1.3) was used in immunocytochemistry on human samples (fig 1). Hum Mol Genet (2015) ncbi
mouse monoclonal (11C1.3)
  • immunohistochemistry - frozen section; human; 1:1000
  • immunohistochemistry; human; 1:1000
In order to study epidermal morphology and dermal composition in individuals of diverese geographic ancestry, Invitrogen FBN1 antibody (Neomarkers, 11C1.3) was used in immunohistochemistry - frozen section on human samples at 1:1000 and in immunohistochemistry on human samples at 1:1000. Br J Dermatol (2014) ncbi
Abcam
domestic rabbit polyclonal
  • immunohistochemistry - paraffin section; mouse; 1:200; loading ...; fig 4c
  • western blot; mouse; 1:2000; loading ...; fig 6a
Abcam FBN1 antibody (Abcam, ab53076) was used in immunohistochemistry - paraffin section on mouse samples at 1:200 (fig 4c) and in western blot on mouse samples at 1:2000 (fig 6a). Invest Ophthalmol Vis Sci (2021) ncbi
Articles Reviewed
  1. Yu X, Sun N, Yang X, Zhao Z, Su X, Zhang J, et al. Nanophthalmos-Associated MYRF Gene Mutation Causes Ciliary Zonule Defects in Mice. Invest Ophthalmol Vis Sci. 2021;62:1 pubmed publisher
  2. Zoppi N, Chiarelli N, Cinquina V, Ritelli M, Colombi M. GLUT10 deficiency leads to oxidative stress and non-canonical αvβ3 integrin-mediated TGFβ signalling associated with extracellular matrix disarray in arterial tortuosity syndrome skin fibroblasts. Hum Mol Genet. 2015;24:6769-87 pubmed publisher
  3. Langton A, Sherratt M, Sellers W, Griffiths C, Watson R. Geographical ancestry is a key determinant of epidermal morphology and dermal composition. Br J Dermatol. 2014;171:274-82 pubmed publisher