SLMAP anticorps (AA 540-790)

N° du produit ABIN7270147

Cet anticorps Lapin Polyclonal détecte spécifiquement SLMAP dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour SLMAP anticorps (AA 540-790) (ABIN7270147)

Antigène: SLMAP (Sarcolemma Associated Protein (SLMAP))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SLMAP est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-SLMAP anticorps

Épitope: AA 540-790

Fonction: SLMAP Rabbit pAb

Séquence: IDTENLREEK DSEITSTRDE LLSARDEILL LHQAAAKVAS ERDTDIASLQ EELKKVRAEL ERWRKAASEY EKEITSLQNS FQLRCQQCED QQREEATRLQ GELEKLRKEW NALETECHSL KRENVLLSSE LQRQEKELHN SQKQSLELTS DLSILQMSRK ELENQVGSLK EQHLRDSADL KTLLSKAENQ AKDVQKEYEK TQTVLSELKL KFEMTEQEKQ SITDELKQCK NNLKLLREKG NNKPWPWMPM L

Réactivité croisée: Humain, Souris, Rat

Attributs du produit: Polyclonal Antibodies

Purification: Affinity purification

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 540-790 of human SLMAP (NP_009090.2).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,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.

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur SLMAP

Antigène: SLMAP (Sarcolemma Associated Protein (SLMAP))

Autre désignation: SLMAP

Sujet: This gene encodes a component of a conserved striatin-interacting phosphatase and kinase complex. Striatin family complexes participate in a variety of cellular processes including signaling, cell cycle control, cell migration, Golgi assembly, and apoptosis. The protein encoded by this gene is a coiled-coil, tail-anchored membrane protein with a single C-terminal transmembrane domain that is posttranslationally inserted into membranes. Mutations in this gene are associated with Brugada syndrome, a cardiac channelopathy. Alternative splicing results in multiple transcript variants.,SLMAP,SLAP,SLMAP

Poids moléculaire: 31-57kDa/90-95kDa

ID gène: 7871

UniProt: Q14BN4