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anti-DLL3 (DLL3) Antikörper

anti-delta Like Protein 3 Antikörper (DLL3)
Auf finden Sie aktuell 87 delta Like Protein 3 (DLL3) Antikörper von 15 unterschiedlichen Herstellern. Zusätzlich bieten wir Ihnen DLL3 Proteine (16) und DLL3 Kits (8) und viele weitere Produktgruppen zu diesem Protein an. Insgesamt sind aktuell 115 DLL3 Produkte verfügbar.
pu, pudgy, SCDO1

Meistgesuchte Reaktivitäten zu anti-DLL3 (DLL3) Antikörper

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anti-Human DLL3 Antikörper:

anti-Mouse (Murine) DLL3 Antikörper:

anti-Rat (Rattus) DLL3 Antikörper:

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Am meisten referenzierte anti-DLL3 Antikörper

  1. Human Polyclonal DLL3 Primary Antibody für EIA, IF - ABIN951923 : Heuss, Ndiaye-Lobry, Six, Israël, Logeat: The intracellular region of Notch ligands Dll1 and Dll3 regulates their trafficking and signaling activity. in Proceedings of the National Academy of Sciences of the United States of America 2008 (PubMed)
    Zeige alle 3 Referenzen für ABIN951923

  2. Human Polyclonal DLL3 Primary Antibody für EIA, IF - ABIN951924 : Yerges, Klei, Cauley, Roeder, Kammerer, Moffett, Ensrud, Nestlerode, Marshall, Hoffman, Lewis, Lang, Barrett-Connor, Ferrell, Orwoll, Zmuda: High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men. in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research 2009 (PubMed)
    Zeige alle 3 Referenzen für ABIN951924

  3. Human Polyclonal DLL3 Primary Antibody für IF, IHC (p) - ABIN656327 : Maisenbacher, Han, Obrien, Tracy, Erol, Schaffer, Dormans, Zackai, Kusumi: Molecular analysis of congenital scoliosis: a candidate gene approach. in Human genetics 2005 (PubMed)
    Zeige alle 3 Referenzen für ABIN656327

Weitere Antikörper gegen DLL3 Interaktionspartner

Human delta Like Protein 3 (DLL3) Interaktionspartner

  1. The Dll3 was rarely detectable in (zeige PIK3CA Antikörper) the (zeige AKT1 Antikörper) para-carcinoma tissues, but positi (zeige NOTCH1 Antikörper)ve in 82.1% of non-small cell cancer tissues.

  2. Both global haplotype and individual haplotype analyses showed that the haplotypes of SNP1/SNP2/SNP3/SNP4/SNP5 did not correlate with the disease (P >0.05). Together, these data suggest that genetic variants of the DLL3 gene are not associated with CS in the Chinese Han population.

  3. DLL3 was silenced by methylation in human human hepatocellular carcinoma and it negatively regulates the growth of human hepatocellular carcinoma cells.

  4. We suggest that the three human DLL3 mutations associated with spondylocostal dysplasia are also functionally equivalent to the Dll3(neo) null allele in mice.

  5. mutations in DLL3 cause a consistent pattern of abnormal vertebral segmentation in spondylocostal dysostosis

  6. no novel or previously described mutations are present in our cohort, indicating that DLL3 mutations may not be a major cause of congenital scoliosis.

  7. The intracellular region of Notch (zeige NOTCH1 Antikörper) ligands Dll1 (zeige DLL1 Antikörper) and Dll3 regulates their trafficking and signaling activity

Mouse (Murine) delta Like Protein 3 (DLL3) Interaktionspartner

  1. Dll3 overexpression promoted PI3K/Akt (zeige AKT1 Antikörper) signaling through inhibiting Notch (zeige NOTCH1 Antikörper) signaling in lung cancer.

  2. O-fucosylation of DLL3 is required for its function during somitogenesis.

  3. Intriguing changes are observed in the cranio-caudal (zeige CAD Antikörper) borders of multifidus muscle in mutant Dll3 and Lfng (zeige LFNG Antikörper) models of idiopathic scoliosis.

  4. Dll3 has a unique function during T-cell development that is distinct from the role played by the other DSL ligands of Notch (zeige NOTCH1 Antikörper).

  5. Dll3 targets Notch1 (zeige NOTCH1 Antikörper) for lysosomal degradation preventing Notch1 (zeige NOTCH1 Antikörper) from undergoing post-translational processing.

  6. Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm.

  7. DLL3 knockout mice have segmentation and neural defects

  8. Notch (zeige NOTCH1 Antikörper) ligands, including Delta-like1 and 3 and Jagged1 (zeige JAG1 Antikörper) and Jagged2 (zeige JAG2 Antikörper), show distinct expression patterns in the developing and adult brain overlapping that of Notch1 (zeige NOTCH1 Antikörper)

  9. Data describe the genetic interactions between Dll1 (zeige DLL1 Antikörper), Dll3, Mesp2 (zeige Mesp2 Antikörper) and Psen1 (zeige PSEN1 Antikörper), and the roles of Dll1 (zeige DLL1 Antikörper)- and Dll3-Notch (zeige NOTCH1 Antikörper) pathways, with or without Psen1 (zeige PSEN1 Antikörper), in rostrocaudal patterning.

  10. spondylocostal dysostosis (SCD (zeige SCD Antikörper)) is caused by mutation in Delta-like (zeige DLK1 Antikörper) 3 (DLL3), Mesoderm posterior 2 (MESP2 (zeige Mesp2 Antikörper)), and Lunatic fringe (LFNG (zeige LFNG Antikörper)); three genes that are components of the Notch (zeige NOTCH1 Antikörper) signaling pathway.

DLL3 Antigen-Profil

Beschreibung des Gens

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.

Alternative names and synonyms associated with DLL3

  • delta-like 3 (Drosophila) (DLL3) Antikörper
  • delta-like 3 (Drosophila) (Dll3) Antikörper
  • pu Antikörper
  • pudgy Antikörper
  • SCDO1 Antikörper

Bezeichner auf Proteinebene für DLL3

delta-like protein 3 , delta3 , drosophila Delta homolog 3 , M-Delta-3

10683 Homo sapiens
484508 Canis lupus familiaris
505993 Bos taurus
13389 Mus musculus
114125 Rattus norvegicus
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