DLL3
Item Information
Catalog #
Size
Price
Description
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.
Product Overview
Formulation
Purified antibody in PBS with 0.05% sodium azide
Storage
4℃; -20℃ for long term storage
Product Image
Elisa
Figure 1:Black line: Control Antigen (100 ng);Purple line: Antigen (10ng); Blue line: Antigen (50 ng); Red line:Antigen (100 ng)
Western Blot
Figure 2:Western blot analysis using DLL3 mAb against human DLL3 (AA: EXTRA(27-226)) recombinant protein. (Expected MW is 26.5 kDa)
Western Blot
Figure 3:Western blot analysis using DLL3 mAb against HEK293-6e (1) and DLL3 (AA: EXTRA(27-226))-hIgGFc transfected HEK293-6e (2) cell lysate.
Western Blot
Figure 4:Western blot analysis using DLL3 mouse mAb against Hela (1)cell lysate.
Immunohistochemical analysis
Figure 5:Immunofluorescence analysis of Hela cells using DLL3 mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor- 555 phalloidin. Secondary antibody from Fisher (Cat#: 35503)
Immunofluorescence analysis
Figure 6:Flow cytometric analysis of C6 cells using DLL3 mouse mAb (green) and negative control (red).
Immunohistochemical analysis
Figure 7:Immunohistochemical analysis of paraffin-embedded cervical carcinoma tissues using DLL3 mouse mAb with DAB staining.
Immunohistochemical analysis
Figure 8:Immunohistochemical analysis of paraffin-embedded rectal cancer tissues using DLL3 mouse mAb with DAB staining.
For Research Use Only. Not for use in diagnostic procedures.