Anti-MAP2 antibody is a chicken polyclonal antibody that is used in MAP2 immunohistochemistry on paraffin-embedded sections (IHC-P), immunocytochemistry/immunofluorescence (ICC/IF), and western blot (WB). Suitable for mouse and rat samples.
- Cited in over 785 publications
- Tried and trusted by researchers since 2003
- Recombinant fragment protein within human MAP2 as immunogen
Preservative: 0.032% Sodium azide
Constituents: PBS
IHC-P | ICC/IF | WB | |
---|---|---|---|
Mouse | Expected | Expected | Tested |
Rat | Tested | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/10000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Rat | Dilution info 1/5000 - 1/10000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info Use at an assay dependent concentration. | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/50000 | Notes This 280kDa band corresponds to the high molecular weight MAP2a and MAP2b isoforms. Also detects 2 bands at approximately 70 kDa, corresponding to MAPc, since the 70kDa bands are transcripts from the same gene and correspond to the C-terminus of the 280kDa bands. |
Species Rat | Dilution info 1/20000 - 1/100000 | Notes This 280kDa band corresponds to the high molecular weight MAP2a and MAP2b isoforms. Also detects 2 bands at approximately 70 kDa, corresponding to MAPc, since the 70kDa bands are transcripts from the same gene and correspond to the C-terminus of the 280kDa bands. |
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The exact function of MAP2 is unknown but MAPs may stabilize the microtubules against depolymerization. They also seem to have a stiffening effect on microtubules.
Microtubule-associated protein 2, MAP-2, MAP2
Anti-MAP2 antibody is a chicken polyclonal antibody that is used in MAP2 immunohistochemistry on paraffin-embedded sections (IHC-P), immunocytochemistry/immunofluorescence (ICC/IF), and western blot (WB). Suitable for mouse and rat samples.
- Cited in over 785 publications
- Tried and trusted by researchers since 2003
- Recombinant fragment protein within human MAP2 as immunogen
Preservative: 0.032% Sodium azide
Constituents: PBS
Lipid extraction from egg yolk, followed by ammonium sulphate precipitation.
Anti-MAP2 antibody (ab5392) is a chicken polyclonal antibody and is validated for use in ICC/IF, IHC-P and WB.
Anti-MAP2 antibody (ab5392) was first used in a scientific publication in 2006 and has been cited over 788 times in peer reviewed journals. It's performance in IHC and Immunofluorescence in human, mouse and rat samples is trusted by the scientific community.
Abcam's high quality validation processes ensure Anti-MAP2 antibody (ab5392) has high sensitivity and specificity.
Anti-MAP2 antibody (ab5392) has 62 independent reviews from customers.
Anti-MAP2 antibody (ab5392) specifically detects MAP2 (UniProt ID: P11137; Molecular weight: 200kDa) and is sold in 25 µL selling sizes.
MAP2, a dendritic marker, plays a crucial role in Alzheimer's disease (AD) research. Researchers use MAP2 to assess dendritic integrity in AD models, making it essential for understanding neuronal structure and pathology in Alzheimer's disease.
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MAP2 also known as Microtubule-associated protein 2 is a critical component in cellular mechanics. It aids in the stabilization and assembly of microtubules essential for maintaining the cytoskeleton structure. MAP2 has a molecular mass of approximately 280 kDa. It is highly expressed in the dendrites of neurons in the central nervous system. This expression pattern underlines its importance in dendritic development and maintenance. Though largely neuron-specific minor expression occurs in other tissues but with significantly less intensity.
MAP2 plays a role in maintaining neuronal structure. It participates in the formation of the cytoskeleton by binding to tubulin subunits in microtubules. By doing so it supports the outgrowth of dendrites critical for synaptic connections and neuronal communication. MAP2 does not typically form part of a complex but associates dynamically with other microtubule proteins to regulate microtubule dynamics. Its role extends to influencing the morphology of neurons which impacts information processing and neurotransmission.
MAP2 factors significantly into the regulation of the MAP kinase signaling pathway among others involving cytoskeletal remodeling. It interfaces with pathways controlled by proteins like MAP kinase affecting downstream targets involved in cellular growth and differentiation. MAP2 also interacts with tau proteins both being integral microtubule-associated proteins fostering structural support and transport within neurons.
MAP2 has a connection to neurodegenerative diseases such as Alzheimer's. Abnormal phosphorylation of MAP2 like that observed in tau leads to defective microtubule stability implicating it in neuronal dysfunction associated with Alzheimer's. Additionally some evidence points to MAP2's involvement in schizophrenia where altered dendritic morphology parallels changes in MAP2 expression. Its interaction with other microtubule-associated proteins especially tau further supports its relevance in disease pathology.
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This species and application combination has not been tested, but we predict it will work based on strong homology. However, this combination is not covered by our product promise.
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MAP2 immunofluorescence staining of rat cortical neurons and glia using chicken anti-MAP2 antibody
Rat E20 cultured cortical neuron-glial cells stained for MAP2 (red) using ab5392 at 1/10000 dilution for ICC/IF. Tau is detected with a mouse monoclonal anti-Tau antibody (green). The nuclear counter stain is DAPI (blue). Overlap of MAP2 and Tau staining results in an orange-yellow color.
MAP2 immunofluorescence staining of mouse neurons using chicken anti-MAP2 antibody
ab5392 at a dilution of 1/10000 staining MAP 2 (green) in tissue cultured rat cortical neurons by immunofluorescence. Nuclei are stained blue with Dapi.
All lanes: Western blot - Anti-MAP2 antibody (ab5392) at 1/50000 dilution
Lane 1: Adult rat brain lysate
Lane 2: Embryonic E20 rat brain lysate
Lane 3: Adult mouse brain lysate
Predicted band size: 199 kDa
MAP2 immunofluorescence staining of rat cortical neurons and glia using chicken anti-MAP2 antibody
Rat cortical neurons and glia in mixed tissue culture stained with ab5392 (Chicken antibody to MAP2) (green)(1:30 000) a mouse monoclonal antibody to GFAP (red) and nuclei of all cells stained with Hoechst dye (blue).
MAP2 immunofluorescence staining of rat cortical neurons and glia using chicken anti-MAP2 antibody
ab5392 staining MAP2 in mouse neurons by immunocytochemistry/ immunofluorescence. Cells were PFA fixed and permeabilized in 0.4% Triton X-100 prior to blocking in 5% serum for 1 hour at 25°C. The primary antibody was diluted 1/10000 and incubated with the sample for 20 hours at 21°C. Alexa fluor® 488 goat polyclonal to chicken IgY diluted 1/400 was used as the secondary antibody.
All lanes: Western blot - Anti-MAP2 antibody (ab5392) at 1/10000 dilution
All lanes: Mouse brain lysate - post nuclear supernatant at 10 µg
All lanes: HRP-conjugated rabbit anti-chicken IgY at 1/10000 dilution
Developed using the ECL technique.
Performed under reducing conditions.
Predicted band size: 199 kDa
Observed band size: 280 kDa, 70 kDa
Exposure time: 1min
MAP2 immunohistochemistry staining of rat cerebellum using chicken anti-MAP2 antibody
Chromogenic Immunostaining of a formalin fixed paraffin embedded rat cerebellum section with chicken pAb to MAP2A/B dilution 1/10000, detected in DAB (brown) following the ABC method. Hematoxylin (blue) was used as the counterstain. ab5392 detects neuronal cells, specifically their perikarya and dendrites. Note the prominent staining of Purkinje cells and their dendrites in the molecular layer and staining of the much smaller granule neurons in the granular layer.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary neural/glia cell cells labelling Shootin-1 with Anti-Shootin-1 antibody [EPR29089-46] ab322654 at 1/100 (5.06 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green).
Confocal image showing cytoplasmic staining in mouse primary neural/glia cell (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Confocal scanning Z step was set as 0.3um followed by image processing with maximum Z projection. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab5392 Anti-MAP2 chicken polyclonal antibody was used to counterstain tubulin at 1/ 500 4ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1: Anti-Shootin-1 antibody [EPR29089-46] ab322654 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/ 1000 2ug/ml dilution.
-ve control 2: ab5392 Anti-MAP2 chicken polyclonal antibody at 1/ 500 4ug/ml dilution, followed by Goat Anti-Chicken IgY H&L (Alexa Fluor® 647) ab150171 Goat Anti-Chicken IgY H&L (Alexa Fluor® 647) antibody at 1/1000 dilution.
Immunofluorescent analysis of 4% Paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat primary neural/glia cell cells labelling Shootin-1 with Anti-Shootin-1 antibody [EPR29089-46] ab322654 at 1/100 (5.06 ug/ml) dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed antibody at 1/1000 2ug/ml dilution (Green).
Confocal image showing cytoplasmic staining in rat primary neural/glia cell (shown in green). The counterstain was observed in magenta. Nuclear DNA was labelled with DAPI (shown in blue). Confocal scanning Z step was set as 0.3 um followed by image processing with maximum Z projection. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
ab5392 Anti-MAP2 chicken polyclonal antibody was used to counterstain tubulin at 1/ab5392 500 4ug/ml dilution (Magenta). The Nuclear counterstain was DAPI (Blue).
-ve control 1: Anti-Shootin-1 antibody [EPR29089-46] ab322654 at 1/100 dilution, followed by Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed ab150081 Goat Anti-Rabbit IgG H&L (Alexa Fluor® 488) preadsorbed at 1/ 1000 2ug/ml dilution.
-ve control 2: ab5392 Anti-MAP2 chicken polyclonal antibody at 1/ 500 4ug/ml dilution, followed by Goat Anti-Chicken IgY H&L (Alexa Fluor® 647) ab150171 Goat Anti-Chicken IgY H&L (Alexa Fluor® 647) antibody at 1/1000 dilution.
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