This is a Validated Antibody Database (VAD) review about cow FBN1, based on 5 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: fibrillin-1; MP340
Invitrogen
mouse monoclonal (11C1.3) |
| 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) |
| 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 |
EMD Millipore
mouse monoclonal (11C1.3) |
| In order to report that LTBP-2 is an inhibitor of FGF-2 during wound repair, EMD Millipore FBN1 antibody (Millipore, MAB1919) was used in immunohistochemistry - paraffin section on human samples at 2.5 ug/ml (fig 7b, g). PLoS ONE (2015) ncbi |
mouse monoclonal (11C1.3) |
| EMD Millipore FBN1 antibody (Millipore, MAB1919) was used in immunohistochemistry on human samples at 1:200. Br J Dermatol (2015) ncbi |
mouse monoclonal (11C1.3) |
| EMD Millipore FBN1 antibody (Millipore, MAB1919) was used in immunohistochemistry - paraffin section on human samples at 1:100 (fig 2). Heart Vessels (2016) ncbi |
Articles Reviewed
- 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
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