DLL3 anticorps

N° du produit ABIN2459090

Détail du produit anti-DLL3 anticorps

Antigène: DLL3 (delta Like Protein 3 (DLL3))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DLL3 est non-conjugé

Application: Western Blotting (WB), ELISA

Purification: Antibody is purified by peptide affinity chromatography method.

Immunogène: Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human DLL3.

Information d'application

Indications d'application: DLL3 antibody can be used for detection of DLL3 by ELISA at 1:312500. DLL3 antibody can be used for detection of DLL3 by western blot at 1 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Reconstitution: Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

Concentration: 1 mg/mL

Buffer: Antibody is lyophilized in PBS buffer with 2 % sucrose.

Conseil sur la manipulation: As with any antibody avoid repeat freeze-thaw cycles.

Stock: 4 °C/-20 °C

Stockage commentaire: For short periods of storage (days) store at 4 °C. For longer periods of storage, store DLL3 antibody at -20 °C.

Détails sur DLL3

Antigène: DLL3 (delta Like Protein 3 (DLL3))

Autre désignation: DLL3 (DLL3 Produits)

Synonymes: anticorps SCDO1, anticorps pu, anticorps pudgy, anticorps delta like canonical Notch ligand 3, anticorps delta-like 3 (Drosophila), anticorps DLL3, anticorps Dll3

Sujet: DLL3 is a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene.

Poids moléculaire: 54 kDa

ID gène: 10683

NCBI Accession: NP_058637

UniProt: Q9NYJ7

Pathways: Signalisation Notch