Name: | Mouse monoclonal antibody to vimentin |
Immunogen: | Full length recombinant human vimentin protein , PROT-r-Vim, expressed in and purified from E. coli. |
HGNC Name: | VIM |
UniProt: | P08670 |
Molecular Weight: | 50kDa |
Host: | Mouse |
Isotype: | IgG1 |
Species Cross-Reactivity: | Human, Rat, not Mouse |
RRID: | AB_2572396 |
Format: | Purified antibody at 1mg/mL in 50% PBS, 50% glycerol plus 5mM NaN3 |
Applications: | WB, IF/ICC, IHC |
Recommended Dilutions: | WB: 1:10,000. IF/ICC and IHC: 1:5,000. |
Storage: | Stable at 4°C for one year, for longer term store at -20°C |
Mouse Monoclonal Antibody to Vimentin
Cat# MCA-2A52
$120.00 – $800.00
Vimentin is a protein subunit of the intermediate or 10nm filaments found in the cytoplasm of many cell types (1). Intermediate filaments are relatively stable fibrous components of cells which appear to have primarily a mechanical function. Many cell lines such as HEK293, HeLa, 3T3 and Cos cells contain prominent vimentin networks (1). Vimentin is a major protein of eye lens and cornea, and found generally in mesenchymal tissues in adult mammals. In the CNS it is found in endothelia and developing neurons, developing and some mature astrocytes, microglia, mature Bergmann glia and ependyma (2,3). Mutations in the vimentin gene may cause cataracts (4,5), and elevated levels of vimentin in blood samples are associated with onset of cancer (6,7). Vimentin levels increase in a variety of cell types as they become cancerous, suggesting that increase in expression of this protein is a useful diagnostic marker of the epithelial-mesenchymal transition (8).
The MCA-2A52 was made against full length recombinant human vimentin expressed in and purified from E. coli, EnCor product PROT-r-Vim. Antibodies to vimentin are useful in studies of stem cells and generally to reveal the intermediate filament cytoskeleton. The immunogen used to generate this antibody was full length recombinant human vimentin, PROT-r-Vim, expressed in and purified from E. coli. The same immunogen was used to produce another monoclonal antibody to vimentin MCA-2D1. We recently found that both monoclonal antibodies bind to a region in the C-terminal “tail” region of vimentin included in the peptide SRISLPLPNFSSLNLRE, which is conserved in rat, cow, pig and most other species. Interestingly mouse has the peptide SRISLPLPTFSSLNLRE, differing by just one amino acid, a threonine substituted for a asparagine. As a result neither MCA-2A52 nor MCA-2D1 bind this peptide. These antibodies can therefore be used to identify human or rat cells in a background of mouse cultures or tissues.hese antibodies can therefore be used to identify human or rat cells in a background of mouse cultures or tissues. We also market a very popular chicken polyclonal antibody to vimentin, CPCA-Vim and also a rabbit polyclonal to vimentin RPCA-VIM. These two antibodies bind vimentin expressed in a wide variety of species including mouse, rat and human. Mouse select image above left for larger view.
Chromogenic immunostaining of a 4% PFA fixed paraffin embedded rat kidney section with mouse mAb to vimentin, MCA-2A52, dilution 1:2,000, detected in DAB (brown) using the Vector Labs ImmPRESS method and reagents with citra buffer retrieval. Hematoxylin (blue) was used as the counterstain. The MCA-2A52 antibody labels tubular epithelium in kidney. This antibody performs well in testing with both 4% PFA and standard NBF fixed tissues but does not stain long term NBF fixed tissue effectively.Mouse select image for larger view.
We recently found that this antibody, an IgG1 and MCA-2D1, an IgG2a, both failed to bind mouse tissues although they work well on human, rat and many other species. This allowed us to firmly map the epitope for both antibodies to the peptide SRISLPLPNFSSLNREL, amino acids 409-425 of the human sequence. This peptide is located at the beginning of the non-helical “tail” region of the molecule and the peptide is totally conserved in most mammalian species including, besides human and rat, cow, pig, horse, camel and many monkeys. These findings increase the general utility of these reagents. A sequence alignment of the human, rat and mouse vimentin sequences can be downloaded here.
1. Franke WW, et al. Different intermediate-sized filaments distinguished by immunofluorescence microscopy. PNAS 75:5034–8 (1978).
2. Dahl D, et al. Vimentin, the 57 000 molecular weight protein of fibroblast filaments, is the major cytoskeletal component in immature glia. Eur. J. Cell Biol. 24:191-6 (1981).
3. Shaw, G. et al. An immunofluorescence microscopical study of the neurofilament triplet proteins, vimentin and glial fibrillary acidic protein within the adult rat brain. Eur. J. Cell Biol. 26:68-72 (1981).
4. Muller M, et al. Dominant cataract formation in association with a vimentin assembly disrupting mutation. Hum. Molec. Genet. 18:1052-7 (2009).
5. Zhai Y, et al. Targeted exome sequencing of congenital cataracts related genes: broadening the mutation spectrum and genotype-phenotype correlations in 27 Chinese Han families. Sci. Rep. 7:1219 (2017).
6. Satelli A, Li S. Vimentin in cancer and its potential as a molecular target for cancer therapy. Cell Mol. Life Sci. 68:3033-46 (2011).
7. Wong KF, Luk JM. Discovery of lamin B1 and vimentin as circulating biomarkers for early hepatocellular carcinoma. Meth. Mol. Biol. 2909:295-310 (2012).
8. Jia X, et al. Vimentin-a potential biomarker for therapeutic efficiency of HAART. Acta Biochim. Biophys. Sin. (Shanghai) 6:1001-6 (2014).
This antibody is new but has been utilized in peer reviewed publications. We will add new citations below as we become aware of them.
1. Sandhu MS, et al. Intraspinal transplantation of subventricular zone-derived neural progenitor cells improves phrenic motor output after high cervical spinal cord injury. Exp. Neurol. 287:205-15 (2017).
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Contact info
EnCor Biotechnology Inc.
4949 SW 41st Boulevard, Ste 40
Gainesville
Florida 32608 USA
Phone: (352) 372 7022
Fax: (352) 372 7066
E-mail: admin@encorbio.com