×
For best experience we recommend to activate Javascript in your browser.
DLL3 antibody (AA 62-286)
DLL3
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-DLL3 Antibody
(hide)
Target
See all DLL3 Antibodies
DLL3
(delta Like Protein 3 (DLL3))
Binding Specificity
All epitopes for DLL3 antibodies
AA 62-286
Reactivity
All reactivities for DLL3 antibodies
Human
Host
All hosts for DLL3 antibodies
Rabbit
Clonality
All clonalities for DLL3 antibodies
Polyclonal
Conjugate
All conjugates for DLL3 antibodies
This DLL3 antibody is un-conjugated
Application
All applications for DLL3 antibodies
Western Blotting (WB)
Purification
Protein A Chromatography
Immunogen
A partial length recombinant Delta like 3 protein (amino acids 62-286) was used as the immunogen for this antibody.
Isotype
IgG
Top Product
Discover our top product DLL3 Primary Antibody
Alternatives
(show)
Application Details
(hide)
Application Notes
WB: 2-4 μg/mL
Restrictions
For Research Use only
Handling
(hide)
Concentration
0.5 mg/mL
Buffer
PBS containing 0.05 % BSA, PH 7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C/-20 °C
Storage Comment
Store the antibody at 4°C, stable for 6 months. For long-term storage, store at -20°C. Avoid repeated freeze and thaw cycles.
Target Details for DLL3
(hide)
Target
DLL3
(delta Like Protein 3 (DLL3))
Alternative Name
Delta like 3 (DLL3 Products )
Synonyms
SCDO1 antibody, pu antibody, pudgy antibody, delta like canonical Notch ligand 3 antibody, delta-like 3 (Drosophila) antibody, DLL3 antibody, Dll3 antibody
Background
Delta like 3 (DLL3) is a member of Delta/Serrate/Lag2 (DSL) ligands for Notch receptors and plays a role in Notch signaling. Out of Five DSL ligands, DLL3 is the most structurally divergent DSL ligand. DLL3 is expressed throughout the presomitic mesoderm and is localized to the rostral somatic compartments. Homozygous disruptions of Notch1 and DLL3 result in severe abnormalities in somitogenesis. Mutations in the human DLL3 homolog cause recessive skeletal abnormalities in spondylocostal dysostosis with a consistent pattern of abnormal segmentation.
Molecular Weight
65 kDa
Gene ID
10683
UniProt
Q9NYJ7
Pathways
Notch Signaling
Recently viewed
(hide)