Technical Support: menoci@medizin.uni-goettingen.de
Department of Medical Informatics
University Medical Center Göttingen
Imprint
View primary antibody
Basic data
| PID | primary-0815 |
| EPIC PID | https://hdl.handle.net/21.11124/primary-0815 |
| Research group | RG Lehnart |
| Quality (mean) | no score (0.00) |
| Sharing level | Public |
Antibody data
| Antigen symbol | VCL |
| Antibody Registry ID(s) | AB_477629 |
| Name | Monoclonal Anti-Vinculin antibody |
| Alternative name | metavinculin |
| Lab ID | |
| Tag / Fluorophore | |
| Raised in | Mouse |
| Reacts with | bovine, canine, mouse, rat, turkey, human, chicken, frog |
| Clone | hVIN-1 |
| Isotype | IgG1 |
| Clonality | monoclonal |
| Demasking | unknown |
| Antigen | purified human vinculin from uterus. |
| Crafted By | company |
| Company / Manufacturer | Sigma-Aldrich |
| Catalog no. | V9131 |
| Lot no. | |
| Description | immunohistochemistry (frozen sections): suitable indirect immunofluorescence: 1:400 using cultured human fibroblasts western blot: 1:200 using extract of human fibroblasts |
| Localization | |
| Storage instruction | storage temp. −20°C |
| Receipt date | 2021-10-25 00:00:00 |
| Preparation date | 2021-10-25 00:00:00 |
| Created by | Klauenberg, Vanessa |
| Last modified | Klauenberg, Vanessa |
External links
Applications
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Linked publications
The oxidation-resistant CaMKII-MM281/282VV mutation does not prevent arrhythmias in CPVT1
Sadredini M, Manotheepan R, Lehnart SE, Anderson ME, Sjaastad I, Stokke MK
Physiol Rep 2021 : 10.14814/phy2.15030
Generation of a genetically-modified induced pluripotent stem cell line harboring an oncogenic gene variant KRAS p.G12V
Busley AV, Kleinsorge M, Cyganek L
Stem Cell Res 2023 : 10.1016/j.scr.2023.103105
Generation of a genetically-modified induced pluripotent stem cell line harboring a Noonan syndrome-associated gene variant MRAS p.G23V
Busley AV, Cyganek L
Stem Cell Res 2023 : 10.1016/j.scr.2023.103108
An Alternative Mechanism of Subcellular Iron Uptake Deficiency in Cardiomyocytes
Dai Y, Ignatyeva N, Xu H, Wali R, Toischer K, Brandenburg S, Lenz C, Pronto J, Fakuade FE, Sossalla S, Zeisberg EM, Janshoff A, Kutschka I, Voigt N, Urlaub H, Rasmussen TB, Mogensen J, Lehnart SE, Hasenfuss G, Ebert A
Circ Res 2023 : 10.1161/circresaha.122.321157
Mutation-induced LZTR1 polymerization provokes cardiac pathology in recessive Noonan syndrome
Busley AV, Gutiérrez-Gutiérrez O, Hammer E, Koitka F, Mirzaiebadizi A, Steinegger M, Pape C, Böhmer L, Schroeder H, Kleinsorge M, Engler M, Cirstea IC, Gremer L, Willbold D, Altmüller J, Marbach F, Hasenfuss G, Zimmermann WH, Reza Ahmadian M, Wollnik B, Cyganek L
Cell Rep 2024 : 10.1016/j.celrep.2024.114448
