Emerin anticorps (N-Term)

N° du produit ABIN2789365

Cet anticorps anti-Emerin Polyclonal Lapin (ABIN2789365) détecte spécifiquement Emerin dans WB. L’anticorps est réactif avec des échantillons de Humain, Souris, Rat, Lapin, Cobaye, Boeuf (Vache), Chien et Cheval.

Aperçu rapide pour Emerin anticorps (N-Term) (ABIN2789365)

Antigène: Emerin (EMD)

Reactivité: Humain, Souris, Rat, Lapin, Cobaye, Boeuf (Vache), Chien, Cheval

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Emerin est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-Emerin anticorps

Épitope: N-Term

Fonction: EMD Antibody - N-terminal region

Séquence: YEKKIFEYET QRRRLSPPSS SAASSYSFSD LNSTRGDADM YDLPKKEDAL

Homologie: Cow: 92%, Dog: 92%, Guinea Pig: 100%, Horse: 92%, Human: 100%, Mouse: 92%, Rabbit: 83%, Rat: 100%

Attributs du produit: This is a rabbit polyclonal antibody against EMD. It was validated on Western Blot.

Purification: Affinity Purified

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

Commentaires:

We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP63088-100UG

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.5 mg/mL

Buffer: Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

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: prevent freeze-thaw cycles

Stock: 4 °C,-20 °C

Stockage commentaire: For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.

Détails sur Emerin

Antigène: Emerin (EMD)

Autre désignation: EMD

Sujet:

Background Information: Emerin is a serine-rich nuclear membrane protein and a member of the nuclear lamina-associated protein family. It mediates membrane anchorage to the cytoskeleton. Dreifuss-Emery muscular dystrophy is an X-linked inherited degenerative myopathy resulting from mutation in the emerin gene.

Gene Name: Emerin

Alternative Symbols: STA, EDMD, LEMD5

Protein Name: Emerin

Poids moléculaire: 28kDa

ID gène: 2010

NCBI Accession: NP_000108

UniProt: P50402