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Monoclonal Anti-Neurofilament 200 antibody produced in mouse

enhanced validation

clone NE14, ascites fluid

NF200 Antibody - Monoclonal Anti-Neurofilament 200 antibody produced in mouse, Neurofilament Antibody, Nf200 Antibody, Monoclonal Anti-Neurofilament heavy chain
MDL number:

biological source


Quality Level



antibody form

ascites fluid

antibody product type

primary antibodies


NE14, monoclonal

mol wt

antigen apparent mol wt 200 kDa


15 mM sodium azide as preservative

species reactivity

chicken, human, bovine, guinea pig, rabbit, pig, rat, mouse

enhanced validation

independent ( Antibodies)
Learn more about Antibody Enhanced Validation


immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:40
immunohistochemistry (frozen sections): suitable
microarray: suitable
western blot: suitable



UniProt accession no.

shipped in

dry ice

storage temp.


Gene Information

human ... NEFH(4744)

General description

Monoclonal Anti-Neurofilament 200 (mouse IgG1 isotype) is derived from the hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse. The 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 kD, 160 kD, and 200 kD and are named as NEFL (light), NEFM (medium) and NEFH (heavy) respectively. Neurofilament proteins are synthesized in the neuronal perikarya, assembled to form filaments and then slowly transported within the axons towards the synaptic terminals.


pig spinal cord.


Applications in which this antibody has been used successfully, and the associated peer-reviewed papers, are given below.
Immunofluorescence (1 paper)
Immunohistochemistry (1 paper)
Monoclonal Anti-Neurofilament 200 antibody produced in mouse has been used in
  • immunohistochemistry
  • immunolabeling
  • immunofluorescence

Biochem/physiol Actions

Neurofilament heavy chain (NEFH) gene was recently identified to cause autosomal dominant axonal Charcot-Marie-Tooth disease (CMT2cc). This gene plays a role in the pathogenesis of sporadic amyotrophic lateral sclerosis (ALS). The phosphorylation of neurofilament polypeptides has been suggested to modulate their function by influencing the interaction between neurofilament and cytoplasmic organelles.


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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