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Background: |
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. |
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Applications: |
ELISA, IHC |
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Name of antibody: |
DLL3 |
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Immunogen: |
Synthetic peptide of human DLL3 |
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Full name: |
delta like canonical Notch ligand 3 |
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Synonyms: |
SCDO1 |
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SwissProt: |
Q9NYJ7 |
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ELISA Recommended dilution: |
5000-10000 |
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IHC positive control: |
Human esophagus cancer;Human prostate cancer |
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IHC Recommend dilution: |
20-100 |

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