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About This Item
Conjugate:
unconjugated
Clone:
polyclonal
Application:
ARR, IHC (p), WB
Citations:
320
biological source
rabbit
Quality Level
conjugate
unconjugated
antibody form
IgG fraction of antiserum
antibody product type
primary antibodies
clone
polyclonal
form
buffered aqueous solution
mol wt
antigen 200 kDa
species reactivity
bovine, wide range
packaging
antibody small pack of 25 μL
enhanced validation
independent ( Antibodies)
Learn more about Antibody Enhanced Validation
technique(s)
immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:80 using animal cerebellum sections, microarray: suitable, western blot: suitable
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
human ... NEFH(4744)
mouse ... Nefh(380684)
rat ... Nefh(24587)
General description
Neurofilament 200, also known as neurofilament heavy polypeptide (NEFH), is encoded by the gene mapped to human chromosome 22q12.2. The encoded protein has a molecular mass of 200kDa and belongs to the group of type IV intermediate filaments which are key constituents of the neuronal cytoskeleton. NEFH contains C-terminal motifs involved in the formation of sidearm projections which cross-link the neurofilaments.
Immunogen
Neurofilament 200 from bovine spinal cord.
Application
Anti-neurofilament 200 antibody produced in rabbit has been used for immunolabeling.
Anti-neurofilament 200 antibody produced in rabbit has been used:
Anti-neurofilament 200 antibody produced in rabbit has been used:
- for detection of neurofilaments using immunohistological staining
- in human astrocytoma cell line
- in post-mortem brain sections
- in human cremaster muscles
- for detection of neurofilaments by immunofluorescence staining in lumbar spinal cord sections of mice
Biochem/physiol Actions
Neurofilament 200 plays a vital role in cytoarchitecture organization. Downregulated expression of the gene has been observed in schizophrenia patients. Loss of gene expression is associated with the development of prostate carcinoma. Mutation in the gene leads to sporadic amyotrophic lateral sclerosis (ALS).
Neurofilament 200 assembly during development is critical for normal functioning of neuronal cells. Mutations in gene encoding neurofilaments is associated with neurological disorder called the Charcot–Marie–Tooth.
Neurofilament 200 assembly during development is critical for normal functioning of neuronal cells. Mutations in gene encoding neurofilaments is associated with neurological disorder called the Charcot–Marie–Tooth.
Shows a wide species cross-reactivity. Reacts with neurofilaments in the central and peripheral nervous system and localizes the neurofilament polypeptide.
Physical form
Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide.
Preparation Note
Store at -20°C. For continuous use, the product may be stored at 2-8°C for up to one month. For extended storage, solution may be frozen in working aliquots at –20°C. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify by centrifugation before use.
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
12 - Non Combustible Liquids
wgk
WGK 2
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
常规特殊物品
低风险生物材料
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Related Content
Peripherin-mediated death of motor neurons rescued by overexpression of neurofilament NF-H proteins.
Beaulieu JM and Julien JP
Journal of Neurochemistry, 85(1), 248-256 (2003)
Expression pattern of NOGO-A protein in the human nervous system.
Buss A, et al.
Acta Neuropathologica, 110(2), 113-119 (2005)
Neuronal intermediate filaments in amyotrophic lateral sclerosis.
Codron P, et al.
Update on Amyotrophic Lateral Sclerosis (2016)
Global Trade Item Number
| SKU | GTIN |
|---|---|
| N4142-.2ML | 04061834116479 |
| N4142-.5ML | 04061834116486 |