Rabbit Recombinant Monoclonal MAP2 antibody - conjugated to Alexa Fluor® 568. Suitable for IHC-P, ICC/IF and reacts with Human, Mouse, Rat samples.
IgG
Rabbit
Alexa Fluor® 568
Ex: 578nm, Em: 603nm
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 68% PBS, 30% Glycerol (glycerin, glycerine), 1% BSA
Liquid
Monoclonal
IHC-P | ICC/IF | |
---|---|---|
Human | Tested | Expected |
Mouse | Tested | Tested |
Rat | Tested | Tested |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Mouse | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/100 | Notes Perform heat-mediated antigen retrieval with Tris/EDTA buffer pH 9.0 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/250 | Notes - |
Species Rat | Dilution info 1/250 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info Use at an assay dependent concentration. | Notes - |
Select an associated product type
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
Rabbit Recombinant Monoclonal MAP2 antibody - conjugated to Alexa Fluor® 568. Suitable for IHC-P, ICC/IF and reacts with Human, Mouse, Rat samples.
Microtubule-associated protein 2, MAP-2, MAP2
IgG
Rabbit
Alexa Fluor® 568
Ex: 578nm, Em: 603nm
pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 68% PBS, 30% Glycerol (glycerin, glycerine), 1% BSA
Liquid
Monoclonal
EPR19691
Affinity purification Protein A
Blue Ice
1-2 weeks
+4°C
-20°C
Upon delivery aliquot
Avoid freeze / thaw cycle, Store in the dark
Our RabMAb® technology is a patented hybridoma-based technology for making rabbit monoclonal antibodies. For details on our patents, please refer to RabMAb® patents.
This product is a recombinant monoclonal antibody, which offers several advantages including:
For more information, read more on recombinant antibodies.
Alexa Fluor® is a registered trademark of Molecular Probes, Inc, a Thermo Fisher Scientific Company. The Alexa Fluor® dye included in this product is provided under an intellectual property license from Life Technologies Corporation. As this product contains the Alexa Fluor® dye, the purchase of this product conveys to the buyer the non-transferable right to use the purchased product and components of the product only in research conducted by the buyer (whether the buyer is an academic or for-profit entity). As this product contains the Alexa Fluor® dye the sale of this product is expressly conditioned on the buyer not using the product or its components, or any materials made using the product or its components, in any activity to generate revenue, which may include, but is not limited to use of the product or its components: in manufacturing; (ii) to provide a service, information, or data in return for payment (iii) for therapeutic, diagnostic or prophylactic purposes; or (iv) for resale, regardless of whether they are sold for use in research. For information on purchasing a license to this product for purposes other than research, contact Life Technologies Corporation, 5781 Van Allen Way, Carlsbad, CA 92008 USA or outlicensing@thermofisher.com.
We have tested this species and application combination and it works. It is covered by our product promise.
We have not tested this specific species and application combination in-house, but expect it will work. It is covered by our product promise.
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.
We do not recommend this combination. It is not covered by our product promise.
We are dedicated to supporting your work with high quality reagents and we are here for you every step of the way should you need us.
In the unlikely event of one of our products not working as expected, you are covered by our product promise.
Full details and terms and conditions can be found here:
Terms & Conditions.
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue labeling MAP2 with ab303465 at 1/100 dilution (5.0 µg/mL). Positive staining is observed on human cerebrum. The section was incubated with ab303465 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND®RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 40 mins was used.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue labeling MAP2 with ab303465 at 1/100 dilution (5.0 µg/mL). Positive staining is observed on mouse cerebrum. The section was incubated with ab303465 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND®RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 40 mins was used.
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue labeling MAP2 with ab303465 at 1/100 dilution (5.0 µg/mL). Positive staining is observed on rat cerebrum. The section was incubated with ab303465 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.The immunostaining was performed on a Leica Biosystems BOND®RX instrument. Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution 2) for 40 mins was used.
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized mouse primary neuron cells labeling MAP2 with ab303465 at 1/250 dilution (2 μg/ml) (Red). Confocal image showing positive staining in mouse primary neuron. Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection. Anti-MAP2 antibody [HM-2] ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain tubulin at 1/500 4 μg/ml dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) (Green). The Nuclear counterstain was DAPI (Blue).
Immunofluorescent analysis of 4% paraformaldehyde-fixed, 0.1% TritonX-100 permeabilized rat primary neuron cells labeling MAP2 with ab303465 at 1/250 dilution (2 ug/ml) (Green). Confocal image showing positive staining in rat primary neuron. Confocal scanning Z step was set as 0.3 μm, followed by image processing with maximum Z projection. Anti-MAP2 antibody [HM-2] ab11267 Anti-MAP2 mouse monoclonal antibody was used to counterstain tubulin at 1/500 4 μg/ml dilution, followed by Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) ab150113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) (Green). The Nuclear counterstain was DAPI (Blue).
Immunocytochemical analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized rat primary neurons staining MAP2 using ab303465 at a 1/250 dilution (2 μg/ml) (Red). Counterstained with Anti-MAP2 antibody [HM-2] ab11267 Anti-MAP2 mouse monoclonal antibody at a 1/500 dilution (4 μg/ml), followed by ab50113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) at a 1/1000 dilution (2 μg/ml) (Green). Nuclear counterstain is DAPI (Blue).
Confocal image showing positive staining in rat primary neuron.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
Immunocytochemical analysis of 4% paraformaldehyde-fixed, 0.1% Triton X-100 permeabilized mouse primary neurons staining MAP2 using ab303465 at a 1/250 dilution (2 μg/ml) (Red). Counterstained with Anti-MAP2 antibody [HM-2] ab11267 Anti-MAP2 mouse monoclonal antibody at a 1/500 dilution (4 μg/ml), followed by ab50113 Goat Anti-Mouse IgG H&L (Alexa Fluor® 488) at a 1/1000 dilution (2 μg/ml) (Green). Nuclear counterstain is DAPI (Blue).
Confocal image showing positive staining in mouse primary neuron.
Confocal scanning Z step was set as 0.3 μm followed by image processing with maximum Z projection.
Immunohistochemical analysis of paraffin-embedded mouse cerebrum tissue stained for MAP2 using ab303465 at a 1/100 dilution (5.0 μg/ml) (Red). Positive staining on mouse cerebrum.
The section was incubated with Alexa Fluor® 647 Anti-CD127 antibody [EPR23747-333] ab303455 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.
The immunostaining was performed on a Leica Biosystems BOND RX instrument.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 40 mins).
Immunohistochemical analysis of paraffin-embedded human cerebrum tissue stained for MAP2 using ab303465 at a 1/100 dilution (5.0 μg/ml) (Red). Positive staining on human cerebrum.
The section was incubated with Alexa Fluor® 647 Anti-CD127 antibody [EPR23747-333] ab303455 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.
The immunostaining was performed on a Leica Biosystems BOND RX instrument.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 40 mins).
Immunohistochemical analysis of paraffin-embedded rat cerebrum tissue stained for MAP2 using ab303465 at a 1/100 dilution (5.0 μg/ml) (Red). Positive staining on rat cerebrum.
The section was incubated with Alexa Fluor® 647 Anti-CD127 antibody [EPR23747-333] ab303455 for 60 mins at room temperature (shown in red). Nuclear DNA was labeled with DAPI (shown in blue). The section was then mounted using Fluoromount®.
The immunostaining was performed on a Leica Biosystems BOND RX instrument.
Image was taken with a confocal microscope (Leica-Microsystems, TCS SP8).
Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0, epitope retrieval solution2) for 40 mins).
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