NEFL anticorps (AA 400-543)

N° du produit ABIN5699797

Cet anticorps Lapin Polyclonal détecte spécifiquement NEFL dans WB, IHC, IF, ELISA et IP. Il présente une réactivité envers Humain, Rat et Souris.

Aperçu rapide pour NEFL anticorps (AA 400-543) (ABIN5699797)

Antigène: NEFL (Neurofilament, Light Polypeptide (NEFL))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NEFL est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), ELISA, Immunoprecipitation (IP)

Détail du produit anti-NEFL anticorps

Épitope: AA 400-543

Fonction: NEFL antibody

Immunogène:

Immunogen sequence: 400-543aa

Immunogen: neurofilament, light polypeptide

Isotype: IgG

Information d'application

Indications d'application: WB: 1:500 - 1:2000, IHC: 1:100 - 1:500, IF: 1:50 - 1:200

Commentaires:

mouse brain tissue were subjected to SDS PAGE followed by western blot with FNab05710(NEFL antibody) at dilution of 1:4000

Restrictions: For Research Use only

Stockage

Buffer: PBS with 0.02 % sodium azide and 50 % glycerol pH 7.3,

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze / thaw cycles.

Stock: -20 °C

Stockage commentaire: -20°C for 12 months

Date de péremption: 12 months

Détails sur NEFL

Antigène: NEFL (Neurofilament, Light Polypeptide (NEFL))

Autre désignation: NEFL

Sujet:

Synonyms: Neurofilament light polypeptide (NF-L)|68 kDa neurofilament protein|Neurofilament triplet L protein|NEFL|NF68|NFL

Background: Neurofilaments are type IV intermediate filament heteropolymers composed of light, medium, and heavy chains. Neurofilaments comprise the axoskeleton and they functionally maintain the neuronal caliber. They may also play a role in intracellular transport to axons and dendrites. This gene encodes the light chain neurofilament protein. Mutations in this gene cause Charcot-Marie-Tooth disease types 1F (CMT1F) and 2E (CMT2E), disorders of the peripheral nervous system that are characterized by distinct neuropathies. A pseudogene has been identified on chromosome Y.

Poids moléculaire: 65-68 kDa,140-160 kDa

UniProt: P07196