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Safety Information

MAB364

Sigma-Aldrich

Anti-MAP2A, 2B, 2C Antibody, clone HM-2

ascites fluid, clone HM-2, Chemicon®

Synonym(s):

Anti-MAP-2, Anti-MAP2A, Anti-MAP2B, Anti-MAP2C

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About This Item

UNSPSC Code:
12352203
eCl@ss:
32160702
NACRES:
NA.41

biological source

mouse

Quality Level

antibody form

ascites fluid

antibody product type

primary antibodies

clone

HM-2, monoclonal

species reactivity

bovine, human, quail, rat, chicken, mouse

manufacturer/tradename

Chemicon®

technique(s)

immunohistochemistry: suitable
western blot: suitable

isotype

IgG1

UniProt accession no.

shipped in

wet ice

target post-translational modification

unmodified

Gene Information

human ... MAP2(4133)

Specificity

Shows selective staining of dendritic trees throughout the brain in immunohistochemical staining of brain tissue. In perkinje neurons, staining is restricted to the dendrites distal to the initial dendrite segment. No staining of cell body in mature Perkinje cells but strong staining of cell bodies of developing Perkinje cells from neonatal rats. No detectable staining of axons or non-neuronal cells. Reacts specifically with all forms of MAP2 (MAP2a ~280 kDa, MAP2b ~280 kDa and MAP2c ~70 kDa) as determined by immunoblot. No cross-reactivity observed to other MAPs or tubulin.

Immunogen

Rat brain microtubule-associated protein.

Application

Anti-MAP2A Antibody, 2B, 2C, clone HM-2 detects level of MAP2A & has been published & validated for use in WB, IH.
Immunoblotting at 1:500 using fresh rat brain extract or enriched microtubule protein preparation.

Immunohistochemistry: 1:50 to 1:1000

Optimal working dilution must be determined by the end user.
Research Category
Neuroscience
Research Sub Category
Neuronal & Glial Markers

Neurofilament & Neuron Metabolism

Physical form

Ascites fluid. Liquid with 15 mM sodium azide.

Storage and Stability

Maintain at -20°C in undiluted aliquots for up to 12 months. Avoid repeated freeze/thaw cycles.

Legal Information

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Disclaimer

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.

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Storage Class Code

12 - Non Combustible Liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

JAN Code

MAB364:


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Magnetic resonance spectroscopic imaging for visualization of the infiltration zone of glioma.
A Stadlbauer,M Buchfelder,M T Doelken,T Hammen,O Ganslandt
Central European neurosurgery null
Dendritic HCN2 channels constrain glutamate-driven excitability in reticular thalamic neurons.
Ying, SW; Jia, F; Abbas, SY; Hofmann, F; Ludwig, A; Goldstein, PA
The Journal of Neuroscience null
Redistribution of MAP2 immunoreactivity in the neurohypophysial astrocytes of adult rats during dehydration.
W Matsunaga, S Miyata, T Kiyohara, W Matsunaga, S Miyata, T Kiyohara
Brain Research null
Extracellular serine protease neuropsin (KLK8) modulates neurite outgrowth and fasciculation of mouse hippocampal neurons in culture.
Takuya Oka, Morito Akisada, Akihito Okabe, Katsutoshi Sakurai, Sadao Shiosaka, Keiko Kato
Neuroscience Letters null
N Chen et al.
Neuroscience, 122(4), 985-995 (2003-12-04)
Cell surface glycoconjugates are thought to mediate cell-cell recognition and to play roles in neuronal development and functions. We demonstrated here that exposure of neuronal cells to nanomolar levels of glyco-chains with an N-acetylgalactosamine (GalNAc) residue at the non-reducing termini

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