SAB4200705

Anti-Neurofilament 200 (Phos and Non-Phos) antibody, Mouse monoclonal

clone N52, purified from hybridoma cell culture

• Synonyme(s) : Anti-CMT2CC, Anti-NFH
• Code UNSPSC : 12352203
• Nomenclature NACRES : NA.41

Propriétés

• Forme d'anticorps: purified from hybridoma cell culture
• Type de produit anticorps: primary antibodies
• Clone: N52, monoclonal
• Poids mol.: ~200 kDa
• Espèces réactives: 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
• Numéro d'accès UniProt: P12036
• Conditions d'expédition: dry ice
• Température de stockage: −20°C
• Modification post-traductionnelle de la cible: unmodified
• Informations sur le gène: pig ... NEFH(100156492)

Description

Description générale

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.

Spécificité

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

Actions biochimiques/physiologiques

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.

Forme physique

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

Stockage et stabilité

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.

Clause de non-responsabilité

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.

Informations sur la sécurité

• Code de la classe de stockage: 10 - Combustible liquids
• Point d'éclair (°F): Not applicable
• Point d'éclair (°C): Not applicable