Name: | Mouse Monoclonal to Lamin A/C, LMNA |
Immunogen: | Full length recombinant human lamin A expressed in and purified from E. coli. |
HGNC Name: | LMNA |
UniProt: | P02545 |
Molecular Weight: | 65kDa, 74kDa |
Host: | Mouse |
Isotype: | IgG1 |
Species Cross-Reactivity: | Human, unreactive with rodent |
RRID: | AB_2572339 |
Format: | Purified antibody at 1mg/mL in 50% PBS, 50% glycerol plus 5mM NaN3 |
Applications: | WB, IF/ICC |
Recommended Dilutions: | WB: 1:1,000-1:2,000. IF/ICC 1:1,000. IHC not recommended |
Storage: | Stable at 4°C for one year, for longer term store at -20°C |
Mouse Monoclonal Antibody to Lamin A/C
Cat# MCA-4C4
$120.00 – $800.00
Lamin A and lamin C are members of the intermediate filament protein family and are located in the nucleus where they function as skeletal components of the inner nuclear membrane (1). The two proteins are generated by alternate transcription from the single LMNA gene. Lamin A has a molecular weight of about 74kDa while lamin C is 65kDa. The lamin A protein includes a C-terminal segment of 98 amino acids missing from lamin C, while lamin C has a unique C-terminal 6 amino acid peptide not present in lamin A. As a result antibodies raised against lamin A are very likely bind to lamin C, as is the case with MCA-4C4. During cell division the nuclear lamina breaks down and lamin A/C containing filaments depolymerize, this being regulated by phosphorylation by cyclin dependent protein kinase 1 (CDK1). Mutations in the lamin A/C gene are associated with several serious human diseases, including Emery-Dreifuss muscular dystrophy, familial partial lipodystrophy, limb girdle muscular dystrophy, dilated cardiomyopathy, Charcot-Marie-Tooth disease type 2B1, Hutchinson-Gilford progeria syndrome and Hutchinson-Gilford progeria syndrome (3-6).
The MCA-4C4 was raised against full length recombinant human lamin A, and binds human lamin C also. Ho\ever it does not recognize rodent lamin A or C. Since MCA-4C4 antibody is human specific, it can be used to monitor human material in a rodent background. It works well on western blots and for IF and ICC but is not recommended for IHC. mWe also market a chicken and a rabbit polyclonal antibody to lamin A/C CPCA-LaminAC and RPCA-LaminAC, both with similar properties to MCA-4C4. Mouse select image above left for larger view.
1. Fisher DZ, Chaudhary N, Blobel G. cDNA sequencing of nuclear lamins A and C reveals primary and secondary structural homology to intermediate filament proteins. PNAS 83:6450-54 (1986).
2. McKeon FD, Kirschner MW, Caput D. Homologies in both primary and secondary structure between nuclear envelope and intermediate filament proteins. Nature 319: 463-8 (1986).
3. Bonne G, et al. Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophy. Nat. Genet. 21:285-8 (1999).
4. Novelli G, et al. Mandibuloacral dysplasia is caused by a mutation in LMNA-encoding lamin A/C. Am. J. Hum. Genet. 71:426-31 (2002).
5. De Sandre-Giovannoli A, et al. Homozygous Defects In Lmna, Encoding Lamin A/C Nuclear‐Envelope Proteins, Cause Autosomal Recessive Axonal Neuropathy In Human (Charcot‐Marie‐Tooth Disorder Type 2) And Mouse Am. J. Hum. Genet. 70:726-36 (2002).
6. Liu B and Zhou Z. Lamin A/C, laminopathies and premature ageing. Histol. Histopathol. 23:747-63 (2006).
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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