Sclerostin anticorps (N-Term)

N° du produit ABIN1539331

Cet anticorps Lapin Polyclonal détecte spécifiquement Sclerostin dans WB. Il présente une réactivité envers Humain et Souris.

Aperçu rapide pour Sclerostin anticorps (N-Term) (ABIN1539331)

Antigène: Sclerostin (SOST)

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp Sclerostin est non-conjugé

Application: Western Blotting (WB)

Clone: RB36187

Détail du produit anti-Sclerostin anticorps

Épitope: AA 38-66, N-Term

Homologie: B

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogène: This SOST antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 38-66 amino acids from the N-terminal region of human SOST.

Isotype: Ig Fraction

Information d'application

Indications d'application: WB: 1:1000. WB: 1:500

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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,-20 °C

Stockage commentaire: SOST Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, keep at -20 °C.

Date de péremption: 6 months

Détails sur Sclerostin

Antigène: Sclerostin (SOST)

Autre désignation: SOST

Sujet: Sclerostin is a secreted glycoprotein with a C-terminal cysteine knot-like (CTCK) domain and sequence similarity to the DAN (differential screening-selected gene aberrative in neuroblastoma) family of bone morphogenetic protein (BMP) antagonists. Loss-of-function mutations in this gene are associated with an autosomal-recessive disorder, sclerosteosis, which causes progressive bone overgrowth. A deletion downstream of this gene, which causes reduced sclerostin expression, is associated with a milder form of the disorder called van Buchem disease. [provided by RefSeq].

Poids moléculaire: 24031

ID gène: 50964

NCBI Accession: NP_079513

UniProt: Q9BQB4