SAB4200705
Anti-Neurofilament 200 (Phos and Non-Phos) antibody, Mouse monoclonal
clone N52, purified from hybridoma cell culture
Synonym(s):
Anti-CMT2CC, Anti-NFH
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About This Item
UNSPSC Code:
12352203
NACRES:
NA.41
Recommended Products
antibody form
purified from hybridoma cell culture
Quality Level
antibody product type
primary antibodies
clone
N52, monoclonal
mol wt
~200 kDa
species reactivity
mouse, pig, feline, rat, monkey, bovine, human
concentration
~1.0 mg/mL
technique(s)
immunoblotting: 2.5-5 μg/mL using human neuroblastoma SH-SY5Y cell line fresh lysate
immunofluorescence: suitable
immunohistochemistry: 10 μg/mL using heat-retrieved formalin-fixed, paraffin-embedded human Cerebellum sections
isotype
IgG1
UniProt accession no.
shipped in
dry ice
storage temp.
−20°C
target post-translational modification
unmodified
Gene Information
pig ... NEFH(100156492)
General description
Monoclonal Anti-Neurofilament 200 (phosphorylated and non-phosphorylated) (mouse IgG1 isotype) is derived from the N52 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from an immunized mouse. Neurofilament 200 also known as Neurofilament heavy polypeptide (H-subunit) and is 200 kDa.
Neurofilament 200 is encoded by the gene located at human chromosome 22q12.2.
Specificity
Monoclonal Anti-Neurofilament 200 (Phos. and NonPhos.) also known as Neurofilament-H or Heavy subunit, specifically recognizes an epitope on the C-terminal tail domain of Neurofilament 200, which is present on both the phosphorylated and nonphosphorylated forms of this glycoprotein. The antibody shows reactivity with neurofilaments in the central and peripheral nervous systems from human , pig, mouse, rat, monkey, feline and bovine origin.
Application
Anti-Neurofilament 200 (Phos and Non-Phos) antibody has been used in
- immunoblotting
- immunofluorescence
- immunohistochemistry
Biochem/physiol Actions
Mutation in the NEFH gene leads to the development of autosomal dominant axonal Charcot-Marie-Tooth disease (CMT2cc).
Neurofilament 200 has an important function in axonal transport, axonal plasticity and maintaining the structure of neuronal cytoskeleton. Defects in Neurofilament 200 are a cause of susceptibility to amyotrophic lateral sclerosis (ALS) and these accumulations are a hallmark of pathological lesion.
Physical form
Solution in 0.01 M phosphate buffered saline pH 7.4, containing 15 mM sodium azide as a preservative.
Storage and Stability
For continuous use, store at 2-8°C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.
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
10 - Combustible liquids
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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Kenji Kashiwagi et al.
Investigative ophthalmology & visual science, 44(1), 154-159 (2002-12-31)
To investigate the phosphorylation of the heavy neurofilament subunit (NF-H), which could be deeply involved in axonal transport of retinal ganglion cells (RGCs), in an experimental glaucoma model of chronic elevation of intraocular pressure (IOP) in monkeys. One eye in
Dissociation of axonal neurofilament content from its transport rate
Yuan A, et al.
Testing, 10(7), e0133848-e0133848 (2015)
Alterations of a 200 kDa neurofilament in the rat hippocampus after forebrain ischemia
Kaku Y, et al.
Journal of Cerebral Blood Flow and Metabolism, 13(3), 402-408 (1993)
Harry B M Uylings et al.
Psychiatry research, 183(1), 1-20 (2010-06-12)
The orbitofrontal cortex (OFC) is located on the basal surface of the frontal lobe and is distinguished by its unique anatomical and functional features. Clinical and postmortem studies suggest the involvement of the orbitofrontal cortex in psychiatric disorders. However, the
Y-L Liu et al.
Spinal cord, 47(2), 166-170 (2008-07-30)
Observational cross-section study. The objective of our study was to determine if phosphorylation of aggregated neurofilaments (NFs) would occur in autoimmune-mediated motor neuron injury. Our main hypothesis was that autoimmune-mediated damage of spinal cord motor neurons may influence NF phosphorylation
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