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N2787

Sigma-Aldrich

Monoclonal Anti-Neurofilament 160 antibody produced in mouse

~2 mg/mL, clone RMO44, purified immunoglobulin, buffered aqueous solution

Synonym(s):

Anti-Neurofilament Medium Chain

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.41

biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

RMO44, monoclonal

form

buffered aqueous solution

species reactivity

human, mouse, rat, zebrafish

concentration

~2 mg/mL

technique(s)

immunohistochemistry: suitable
microarray: suitable
western blot: 1-2 μg/mL using extract of SHSy5y human neuroblastoma cells

isotype

IgG1

UniProt accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... NEFM(4741)
mouse ... Nefm(18040)
rat ... Nefm(24588)

Related Categories

General description

Monoclonal Anti- Neurofilament 160 (mouse IgG1 isotype) is derived from the hybridoma RMO44 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with purified mid-sized rat neurofilament (NF-M) subunit. Neurofilaments are one of the five major groups of intermediate filaments (Ifs) and are found predominantly in cells or tissues of neuronal origin. They are composed of three major proteins of apparent molecular weights 68 kDa, 160 kDa and 200 kDa.
Neurofilament 160 (NEFM) is one among the most abundant filaments in post-mitotic neurons.

Immunogen

purified mid-sized rat neurofilament (NF-M) subunit.

Application

Monoclonal Anti-Neurofilament 160 antibody produced in mouse has been used in:
  • enzyme-linked immunosorbent assay (ELISA)
  • western blot analysis
  • immunohistochemistry
  • antibody labelling

Biochem/physiol Actions

Neurofilament 160 (NEFM) associates with the dopamine receptor.
Neurofilament proteins are synthesized in the neuronal perikarya, assembled to form filaments and then slowly transported within the axons towards the synaptic terminals. These molecules undergo post-translational modifications, which results in their heterogeneity including different levels of phosphorylation. The phosphorylation of neurofilament polypeptides has been suggested to modulate their function by influencing their interaction with cytoplasmic organelles.

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.

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

10 - Combustible liquids

WGK

nwg

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


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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beta-Amyloid precursor protein-b is essential for Mauthner cell development in the zebrafish in a Notch-dependent manner
Banote RK, et al.
Developmental Biology, 413(1), 26-38 (2016)
Neurofilaments at a glance
Yuan A, et al.
Journal of Cell Science, 125(14), 3257-3263 (2012)
Distribution patterns of the zebrafish neuronal intermediate filaments inaa and inab
Liao ML, et al.
Journal of Neuroscience Research, 97(2), 202-214 (2019)
Nesreen Zoghoul Alsmadi et al.
Tissue engineering. Part C, Methods, 29(12), 547-557 (2023-09-24)
Traumatic injuries may result in the formation of soft tissue adhesions between peripheral nerves and surrounding soft tissue. These soft tissue adhesions lead to compression and ischemic stress within fascicles due to nonpliability of adhered scar tissue, and nerve tension
Amanda L Jones et al.
Journal of neuroimmunology, 269(1-2), 68-75 (2014-03-19)
Schizophrenia is a severe debilitating brain disorder with a poorly understood aetiology. Among the diverse aetiological clues lies evidence for immune abnormalities in some individuals. The aim of this study was to investigate the frequency and specificity of autoantibodies directed

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