OSTM1 anticorps (Middle Region) (HRP)

N° du produit ABIN8018574

L’anticorps anti-OSTM1 Polyclonal Lapin est utilisé pour la détection de OSTM1 dans des échantillons de Humain. Il a été validé pour WB, IHC et ELISA.

Aperçu rapide pour OSTM1 anticorps (Middle Region) (HRP) (ABIN8018574)

Antigène: OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp OSTM1 est conjugé à/à la HRP

Application: Western Blotting (WB), Immunohistochemistry (IHC), ELISA

Détail du produit anti-OSTM1 anticorps (HRP)

Épitope: Middle Region

Fonction: Anti-OSTM1 Antibody HRP Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins

Purification: Immunogen affinity purified.

Immunogène: A synthetic peptide corresponding to a sequence in the middle region of human OSTM1.

Isotype: IgG

Information d'application

Indications d'application: Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.

Date de péremption: 12 months

Détails sur OSTM1

Antigène: OSTM1 (Osteopetrosis Associated Transmembrane Protein 1 (OSTM1))

Autre désignation: OSTM1

Sujet:

Background: This gene encodes a protein that may be involved in the degradation of G proteins via the ubiquitin-dependent proteasome pathway. The encoded protein binds to members of subfamily A of the regulator of the G-protein signaling (RGS) family through an N-terminal leucine-rich region. This protein also has a central RING finger-like domain and E3 ubiquitin ligase activity. This protein is highly conserved from flies to humans. Defects in this gene may cause the autosomal recessive, infantile malignant form of osteopetrosis.

Gene Full Name: osteoclastogenesis associated transmembrane protein 1

ID gène: 28962

UniProt: Q86WC4