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Invitrogen™ DLL3 Recombinant Human Monoclonal Antibody (7B7)
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Catalog No. PIMA543156
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100 μL
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PIMA543156 100 μL
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Catalog No. PIMA543156 Supplier Invitrogen™ Supplier No. MA543156
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Human Recombinant Monoclonal Antibody

Antibody tested in Indirect ELISA.

Delta-like protein 3 (DLL3) is a ligand for the Notch signaling pathway. It inhibits primary neurogenesis. DLL3 plays a role in the formation of somite boundaries during segmentation of the paraxial mesoderm. Defects in DLL3 are the cause of Spondylocostal dysostosis autosomal recessive type 1 (SCDO1). Mutations in DLL3 gene cause truncal shortening relative to their limbs, which leads to abdominal protrusion, abnormal spinal curvature and sometimes a plagiocephaly-torticollis sequence. It may be required to divert neurons along a specific differentiation pathway.
TRUSTED_SUSTAINABILITY

Specifications

Antigen DLL3
Applications ELISA, Flow Cytometry
Classification Recombinant Monoclonal
Clone 7B7
Concentration 1 mg/mL
Conjugate Unconjugated
Formulation PBS with 50% glycerol and 0.03% ProClin 300; pH 7.4
Gene Dll3
Gene Accession No. Q9NYJ7
Gene Alias delta like canonical Notch ligand 3; Delta3; delta-like 3; delta-like 3 (Drosophila); delta-like protein 3; Dll3; Drosophila Delta homolog 3; M-Delta-3; pu; pudgy; SCDO1
Gene Symbols Dll3
Host Species Human
Immunogen Recombinant Human DLL3 protein.
Purification Method Affinity Chromatography
Quantity 100 μL
Regulatory Status RUO
Primary or Secondary Primary
Gene ID (Entrez) 10683
Target Species Human
Content And Storage -20°C or -80°C if preferred
Product Type Antibody
Form Liquid
Isotype IgG1
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