EnCor Biotechnology

Goat Polyclonal Antibody to MAP2A/B GPCA-MAP2A/B

$300.00
Description

      The CPCA-GFAP antibody was made against full length human recombinant GFAP, Prot-r-GFAP, expressed in and purified from E. coli. We document that the antibody works well not only for western blotting, IF and ICC but also on formalin fixed paraffin embedded sections, select the "Additional Info" for this data. The same GFAP immunogen was used to produce rabbit, RPCA-GFAP, and chicken, CPCA-GFAP polyclonal antibodies. Using different immunogens, EnCor manufactures widely used mouse monoclonal antibodies to GFAP, MCA-5C10, MCA-2A5, and MCA-3E10.

Amount: 100µL of 1mg/mL
Amount: 100µL of 1mg/mL
Immunofluorescent analysis of rat brain stem section stained with goat pAb to MAP2, GPCA-MAP2, dilution 1:2,000 in red, and costained with mouse mAb to MBP, MCA-7D2, dilution 1:5,000, in green. 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 GPCA-MAP2 antibody labels MAP2 protein in the perikarya and dendrites of the most neurons, notably motorneurons in the brain stem, and the MBP antibody stains myelin sheath around axons.
Western blot analysis of whole brain lysates using goat pAb to MAP2, GPCA-MAP2, dilution 1:5,000 in green: [1] protein standard (red), [2] rat, and [3] mouse brain lysate. A band at about 280kDa corresponds to the MAP2A and MAP2B proteins.

Add a short description for this tabbed section

Name: MAP2, goat polyclonal, Cat# GPCA-MAP2
Immunogen: Recombinant human projection domain sequences, amino acids 377-1505, EnCor products Prot-r-MAP2-P1, Prot-r-MAP2-P2 and Prot-r-MAP2-P3.
HGNC Name: MAP2
UniProt: P11137
Molecular Weight: 280kDa by SDS-PAGE
Host: Goat
Species Cross-Reactivity: Human, rat and mouse
RRID: AB_2737286
Format: Purified antibody at 1mg/mL in 50% PBS, 50% glycerol plus 5mM NaN3
Applications: WB, IF/ICC
Recommended Dilutions: WB: 1:2,000. IF/ICC and IHC: 1:1,000-1:2,000.
Storage: Store at 4°C for short term, for longer term at -20°C

      Microtubules are 25nm diameter protein rods found in most kinds of eukaryotic cells and are associated with a family of proteins called microtubule associated proteins (MAPs). MAPs play a crucial role in the regulation of microtubule dynamics and interactions in vivo. MAP2 was originally named as one of the higher molecular weight MAPs with an SDS-PAGE molecular weight of about 280kDa (1-3). There is a single mammalian MAP2 gene which may generates two high molecular weight proteins of ~280kDa name MAP2A and MAP2B and multiple lower molecular weight forms usually named MAP2C and MAP2D which run on SDS-PAGE gels at 60-70kDa. The lower molecular weight forms are found in neurons early in development, but later are replaced by the higher molecular weight forms (2). The MAP2A and MAP2B forms include a protein insert missing in MAP2C and MAP2D which forms fine filamentous protrusions from the sides of brain microtubules referred to as the "projection domain". This antibody was made against the projection domain sequences and so is specific for MAP2A and MAP2B. MAP2 isoforms are expressed only in neuronal perikarya and dendrites so appropriate antibodies are used to identify neurons and dendrites in cell culture and sections (for example 4-8 used EnCor MAP2 antibodies).



Chromogenic immunostaining of a formalin fixed paraffin embedded rat hippocampus section with goat pAb to MAP2, GPCA-MAP2, dilution 1:2,000, detected with DAB (brown) using the Vector Elite ABC-HRP detection and reagents with citra buffer retrieval. Hematoxylin (blue) was used as the counterstain. The GPCA-MAP2 antibody labels the MAP2 protein in the somata and dendrites of most neurons. Mouse select image for larger view.

1. Dehmelt H, Halpain S. The MAP2/Tau family of microtubule-associated proteins.
Genome Biol. 6:204 (2005).
2. Nunez J. Immature and mature variants of MAP2 and tau proteins and neuronal plasticity. Trends Neurosci. 11:477-9 (1998).
3. 2. Vallee R. A taxol-dependent procedure for the isolation of microtubules and microtubule-associated proteins (MAPs). J. Cell Biol. 92:435-42 (1992).
4. Goetz AK, et al. Temporally restricted substrate interactions direct fate and specification of neural precursors derived from embryonic stem cells. PNAS 103:11063-8 (2006).
5. Walton NM et al. Gliotypic neural stem cells transiently adopt tumorigenic properties during normal differentiation. Stem Cells 27:280-9 (2009).
6. Gasser A, et al. An ankyrinG-binding motif is necessary and sufficient for targeting Nav1.6 sodium channels to axon initial segments and nodes of Ranvier. J. Neurosci. 32:7232-43 (2012).
7. Rush AM, et al. Differential modulation of sodium channel Nav1.6 by two members of the fibroblast growth factor homologous factor 2 subfamily. Eur. J. Neurosci. 23:2551-62 (2006).
8. Eckenstein FP, McGovern T, Kern D, Deignan J. Neuronal vulnerability in transgenic mice expressing an inducible dominant-negative FGF receptor. Exp. Neurol. 198:338-49 (2006).

Add a short description for this tabbed section