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Rabbit Recombinant Monoclonal MAP2 antibody - conjugated to Alexa Fluor® 568. Suitable for IHC-P, ICC/IF and reacts with Human, Mouse, Rat samples.

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Images

Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (AB303465), expandable thumbnail
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (AB303465), expandable thumbnail
  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (AB303465), expandable thumbnail
  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (AB303465), expandable thumbnail
  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (AB303465), expandable thumbnail

Key facts

Isotype

IgG

Host species

Rabbit

Conjugation

Alexa Fluor® 568

Excitation/Emission

Ex: 578nm, Em: 603nm

Storage buffer

pH: 7.4
Preservative: 0.02% Sodium azide
Constituents: 68% PBS, 30% Glycerol (glycerin, glycerine), 1% BSA

Form

Liquid

Clonality

Monoclonal

Immunogen

  • The exact immunogen used to generate this antibody is proprietary information.

Reactivity data

Select an application
Product promiseTestedExpectedPredictedNot recommended
IHC-PICC/IF
Human
Tested
Expected
Mouse
Tested
Tested
Rat
Tested
Tested

Tested
Tested

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.

Tested
Tested

Species

Mouse

Dilution info

1/250

Notes

-

Species

Rat

Dilution info

1/250

Notes

-

Expected
Expected

Species

Human

Dilution info

Use at an assay dependent concentration.

Notes

-

Associated Products

Select an associated product type

6 products for Alternative Version

1 products for Alternative Product

Target data

Function

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.

Alternative names

Recommended products

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Rabbit Recombinant Monoclonal MAP2 antibody - conjugated to Alexa Fluor® 568. Suitable for IHC-P, ICC/IF and reacts with Human, Mouse, Rat samples.

Alternative names

Key facts

Isotype

IgG

Conjugation

Alexa Fluor® 568

Excitation/Emission

Ex: 578nm, Em: 603nm

Form

Liquid

Clonality

Monoclonal

Immunogen
  • The exact immunogen used to generate this antibody is proprietary information.
Clone number

EPR19691

Purification technique

Affinity purification Protein A

Concentration
Loading...

Storage

Shipped at conditions

Blue Ice

Appropriate short-term storage duration

1-2 weeks

Appropriate short-term storage conditions

+4°C

Appropriate long-term storage conditions

-20°C

Aliquoting information

Upon delivery aliquot

Storage information

Avoid freeze / thaw cycle, Store in the dark

Notes

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:

  • - High batch-to-batch consistency and reproducibility
  • - Improved sensitivity and specificity
  • - Long-term security of supply
  • - Animal-free batch production

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.

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.

10 product images

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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.

  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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).

  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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).

  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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.

  • Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunocytochemistry/ Immunofluorescence - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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.

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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).

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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).

  • Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465), expandable thumbnail

    Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) - Alexa Fluor® 568 Anti-MAP2 antibody [EPR19691] (ab303465)

    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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Product protocols

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