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DLL3 antibody (C-Term)
DLL3
Reactivity: Human
WB, IF, IHC (p), EIA
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-DLL3 Antibody
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Target
See all DLL3 Antibodies
DLL3
(delta Like Protein 3 (DLL3))
Binding Specificity
All epitopes for DLL3 antibodies
AA 526-556, C-Term
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), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
Specificity
This antibody recognizes DLL3 at C-term .
Cross-Reactivity (Details)
Species reactivity (tested):Human
Purification
Purified through a Protein A column followed by peptide affinity purification
Immunogen
Synthetic peptide - KLH conjugated - corresponding to the C-terminal region (between 526-556aa) of human DLL3.
Isotype
Ig Fraction
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Discover our top product DLL3 Primary Antibody
Alternatives
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Application Details
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Application Notes
Optimal working dilution should be determined by the investigator.
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.25 mg/mL
Buffer
PBS with 0.09 % (W/V) Sodium azide
Preservative
Sodium azide
Precaution of Use
This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Handling Advice
Avoid repeated freezing and thawing.
Storage
4 °C/-20 °C
Storage Comment
Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
Target Details for DLL3
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Target
DLL3
(delta Like Protein 3 (DLL3))
Alternative Name
DLL3 (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 protein 3 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.Synonyms: Delta-3, Delta-like protein 3
Gene ID
10683
NCBI Accession
NP_058637
Pathways
Notch Signaling
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