Anti-200 kD Neurofilament Heavy antibody [RMO-24] (ab78038)
- Product nameAnti-200 kD Neurofilament Heavy antibody [RMO-24]See all 200 kD Neurofilament Heavy primary antibodies ...
- DescriptionMouse monoclonal [RMO-24] to 200 kD Neurofilament Heavy
- SpecificityReacts with Neurofilament Heavy (NF-H), tail domain (phosphate dependent). Dephosphorylation of the NF-H will results in diminished immunoreactivity.
- Tested applicationsWB, IP, ELISA, IHC-P, IHC-Fr more details
- Species reactivityReacts with: Rat, Human
- EpitopeTail domain (Phosphate dependent)
- Positive control
- Storage instructionsShipped at 4°C. Upon delivery aliquot and store at -20°C. Avoid freeze / thaw cycles.
- Storage bufferPreservative: None
- Concentration information loading...
- Clonality Monoclonal
- Clone numberRMO-24
- Light chain typekappa
Our Abpromise guarantee covers the use of ab78038 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
IHC-Fr: Use at an assay dependent dilution.
The antibody has been used successfully on Bouin's and alcohol fixed paraffin embedded or frozen tissue sections. Formalin fixed paraffin embedded tissue sections require pretreatment with trypsin.
ELISA: Use at an assay dependent dilution.
IP: Use at an assay dependent dilution.
WB: Use at an assay dependent dilution. Predicted molecular weight: 112 kDa.
Not yet tested in other applications.
Optimal dilutions/concentrations should be determined by the end user.
- FunctionNeurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber. NF-H has an important function in mature axons that is not subserved by the two smaller NF proteins.
- Involvement in diseaseDefects in NEFH are a cause of susceptibility to amyotrophic lateral sclerosis (ALS) [MIM:105400]. ALS is a neurodegenerative disorder affecting upper and lower motor neurons, and resulting in fatal paralysis. Sensory abnormalities are absent. Death usually occurs within 2 to 5 years. The etiology is likely to be multifactorial, involving both genetic and environmental factors.
- Sequence similaritiesBelongs to the intermediate filament family.
modificationsThere are a number of repeats of the tripeptide K-S-P, NFH is phosphorylated on a number of the serines in this motif. It is thought that phosphorylation of NFH results in the formation of interfilament cross bridges that are important in the maintenance of axonal caliber.
Phosphorylation seems to play a major role in the functioning of the larger neurofilament polypeptides (NF-M and NF-H), the levels of phosphorylation being altered developmentally and coincident with a change in the neurofilament function.
Phosphorylated in the Head and Rod regions by the PKC kinase PKN1, leading to inhibit polymerization.
- 200 kDa neurofilament protein antibody
- NEFH antibody
- Neurofilament H antibody
- Neurofilament heavy polypeptide 200 kD antibody
- Neurofilament heavy polypeptide 200 kDa antibody
- Neurofilament heavy polypeptide 200kD antibody
- Neurofilament heavy polypeptide 200kDa antibody
- Neurofilament heavy polypeptide antibody
- Neurofilament triplet H protein antibody
- NF 200 antibody
- NF H antibody
- NF-H antibody
- NF200 antibody
- NFH antibody
- NFH_HUMAN antibody
References for Anti-200 kD Neurofilament Heavy antibody [RMO-24] (ab78038)
ab78038 has not yet been referenced specifically in any publications.