EnCor Biotechnology

Mouse Monoclonal Antibody to PEA-15 Cat# MCA-4D117

$250.00
Description

      MCA-4D117 was made against a recombinant full length PEA-15 construct expressed in and purified from E. coli. The antibody can be used for western blotting IF, ICC and IHC (see "Additional Info" tab). The antibody highlights a subset of cell bodies in CNS tissues.

Amount: 100µL of 1mg/mL
Amount: 100µL of 1mg/mL
Immunofluorescent analysis of rat brain section stained with mouse mAb to PEA-15, MCA-4D117, dilution 1:1,000 in red, and costained with chicken pAb to MAP2, CPCA-MAP2, dilution 1:5,000 in green. The blue is Hoechst staining of nuclear DNA. Following transcardial perfusion of rat with 4% paraformaldehyde, brain was post fixed for 24 hours, cut to 45μM, and free-floating sections were stained with above antibodies. The PEA-15 antibody labels the cytoplasm of certain presumably neuronal cells which are not labelled by the astrocyte specific GFAP antibody.
Western blot analysis of different tissue lysates using mouse mAb to PEA-15, MCA-4D117, dilution 1:1,000 in green: [1] protein standard (red), [2] rat whole brain, [3] rat cerebellum, [4] mouse whole brain, [5] cow cortex and [6] cow cerebellum. The strong band at about 15kDa corresponds to the PEA-15 protein.

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Name: PEA-15, mouse monoclonal, Cat# MCA-4D117
Immunogen: Full length human PEA-15 as expressed in and purified from E. coli.
HGNC Name: PEA-15
UniProt: Q15121
Molecular Weight: 15kDa
Host: Mouse
Isotype: IgG1
Species Cross-Reactivity: Human, Rat, Mouse, Cow
RRID: AB_2861183
Format: Purified antibody at 1mg/mL in 50% PBS, 50% glycerol plus 5mM NaN3
Applications: WB, ICC/IF, IHC
Recommended Dilutions: WB: 1:1,000-1:2,000. ICC/IF and IHC: 1:500-1:1,000
Storage: Shipped on ice. Store at 4°C for short term, for longer term at -20°C. Avoid freeze / thaw cycles.

      Pea15 was originally isolated as a major low molecular weight of embryonic mouse striatal astrocytes grown in cell culture. Three spots on 2D gels with an apparent molecular weight of 15kDa and isoelectric point 5.1-5.3 were shown to be different forms of one protein. The protein was serine phosphorylated on one site by protein kinase C both in vivo and in vitro and the protein was named "phosphoprotein enriched in astrocytes of 15kDa", hence PEA-15 (1). Subsequent cloning and sequencing revealed a protein well conserved in sequence between mouse and human and which was heavily expressed in brain (2). Independently the same protein was found to be upregulated in fibroblasts and tissues of diabetic patients, and has hence named "protein enriched in diabetes" or PED (3). Immunocytochemical studies showed that the protein was heavily expressed in astrocytes and certain neurons in the CNS of mice, though it is expressed a lower levels ubiquitously (2,4). The protein could be phosphorylated on a second site by either CaMKII or Akt/PKB, and further examination of the amino acid sequence revealed an N-terminal death effector domain (DED), a predominantly α-helical domain found in many proteins which function in the regulation of apoptosis (5). PEA-15 was shown to interact with extracellular signal regulated kinase (ERK, 6) and regulate the nuclear entry of this protein, and several other important interactions with other proteins involved in regulation of apoptosis, glucose metabolism and cell growth have been described (reviewed in 7).



Chromogenic immunostaining of a 4% PFA fixed paraffin embedded rat testes section with mouse mAb to PEA-15, MCA-4D117, dilution 1:1,000, detected with DAB (brown) following the ABC method with citra epitope retrieval. Hematoxylin (blue) was used as the counterstain. This antibody performs well in testing with 4% PFA but does not stain long term NBF fixed tissue effectively. Mouse select image for larger view.

1. Araujo, H. et al. Characterization of PEA-15, a major substrate for protein kinase C in astrocytes. J. Biol. Chem. 268:5911-20 (1993).
2. Estelles, A. et al. The Major Astrocytic Phosphoprotein PEA-15 Is Encoded by Two mRNAs Conserved on Their Full Length in Mouse and Human. J. Biol. Chem. 271:14800-6 (1996).
3. Condorelli, G. et al. PED/PEA-15 gene controls glucose transport and is overexpressed in type 2 diabetes mellitusEMBO J. 17:3858-66 (1998).
4. Sharif, A. et al. The expression of PEA-15 (phosphoprotein enriched in astrocytes of 15 kDa) defines subpopulations of astrocytes and neurons throughout the adult mouse brain. Neurosci. 126:263-75 (2004).
5. Boldin, MP. et al. A novel protein that interacts with the death domain of Fas/APO1 contains a sequence motif related to the death domain. J. Biol. Chem. 271:7795–78 (1995).
6. Ramos, JW. et al. PEA-15 Mediates Cytoplasmic Sequestration of ERK MAP Kinase. Dev. Cell 1:239–50 (2001).
7. Fiory, F. et al. Frontiers: PED/PEA-15, a multifunctional protein controlling cell survival and glucose metabolism. Am. J. Physiol. Endocrinol. Metab. 297:E592-601 (2009).

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