Emerin anticorps (N-Term)

N° du produit ABIN499790

L’anticorps Lapin Polyclonal anti-Emerin a été validé pour WB, IHC (p) et EIA. Il convient pour détecter Emerin dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour Emerin anticorps (N-Term) (ABIN499790)

Antigène: Emerin (EMD)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Emerin est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)

Détail du produit anti-Emerin anticorps

Épitope: N-Term

Specificité: This antibody reacts to Emerin.

Purification: Affinity chromatography purified via peptide column

Immunogène: Emerin antibody was raised against a 19 amino acid peptide from near the amino terminus of human Emerin.

Isotype: IgG

Information d'application

Indications d'application: ELISA. Western blot: 0.5 - 1 μg/mL. Immunohistochemistry.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Stockage

Buffer: PBS containing 0.02 % sodium azide.

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.

Stock: 4 °C

Stockage commentaire: Store the antibody undiluted at 2-8 °C.

Détails sur Emerin

Antigène: Emerin (EMD)

Autre désignation: Emerin

Sujet: Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family that includes proteins such as LAP2 and MAN1. Each family member, including Emerin, has an ~40 amino acid LEM-domains that binds barrier-to-autointegration (BANF1), a conserved chromatin protein that also serves as a host cell component of retroviral integration complexes, including that of HIV. Emerin is anchored at the inner membrane of the nuclear envelope where it binds to nuclear intermediate filaments that are formed by lamin proteins. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.Synonyms: EDMD, EMD, STA

ID gène: 2010

NCBI Accession: NP_000108

UniProt: P50402