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Anti-MAP2 antibody produced in rabbit

affinity isolated antibody

Anti-MAP2C, Anti-MAP2A, Anti-MAP2B

biological source


Quality Level



antibody form

affinity isolated antibody

antibody product type

primary antibodies




buffered aqueous solution

mol wt

55-75 kDa

species reactivity

rat, human, mouse


1 mg/mL


western blot: 1:500-1:1000



immunogen sequence


NCBI accession no.

UniProt accession no.

shipped in

wet ice

storage temp.


Gene Information

human ... MAP2(4133)

General description

The antibody detects endogenous level of total MAP2 protein.


Peptide sequence around aa. 1819-1823 (T-A-A-L-A), according to the protein NP_002365.3

Features and Benefits

Evaluate our antibodies with complete peace of mind. If the antibody does not perform in your application, we will issue a full credit or replacement antibody. Learn more.

Target description

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.

Physical form

Solution in phosphate-buffered saline containing 0.02% sodium azide and 50% glycerol


Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

Storage Class Code

10 - Combustible liquids



Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Certificate of Analysis

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Certificate of Origin

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Christopher Patzke et al.
The Journal of experimental medicine, 213(4), 499-515 (2016-03-24)
Hundreds of L1CAM gene mutations have been shown to be associated with congenital hydrocephalus, severe intellectual disability, aphasia, and motor symptoms. How such mutations impair neuronal function, however, remains unclear. Here, we generated human embryonic stem (ES) cells carrying a
Hong-Jun Kang et al.
Cancer research, 74(16), 4526-4535 (2014-06-18)
The oncogenic fusion gene EWS-WT1 is the defining chromosomal translocation in desmoplastic small round-cell tumors (DSRCT), a rare but aggressive soft tissue sarcoma with a high rate of mortality. EWS-WT1 functions as an aberrant transcription factor that drives tumorigenesis, but
E Collyer et al.
Experimental neurology, 261, 451-461 (2014-08-01)
After an incomplete spinal cord injury (SCI), partial recovery of locomotion is accomplished with time. Previous studies have established a functional link between extension of axon collaterals from spared spinal tracts and locomotor recovery after SCI, but the tissular signals
Yu Okuma et al.
Neuropharmacology, 85, 18-26 (2014-05-27)
Glycyrrhizin (GL) is a major constituent of licorice root and has been suggested to inhibit the release of high mobility group box-1 (HMGB1), a protein considered representative of damage-associated molecular patterns. We found that GL bound HMGB1 but not RAGE
Zhenglin Gu et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 34(41), 13614-13628 (2014-10-10)
Degeneration of basal forebrain (BF) cholinergic neurons is one of the early pathological events in Alzheimer's disease (AD) and is thought to be responsible for the cholinergic and cognitive deficits in AD. The functions of this group of neurons are

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