RELN antibody

Cat.#: 114685

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Product Information

  • Product Name
    RELN antibody
  • Documents
  • Description
    RELN Rabbit Polyclonal antibody. Positive IHC detected in human liver tissue.
  • Tested applications
    ELISA, IHC
  • Species reactivity
    Human; other species not tested.
  • Alternative names
    PRO1598 antibody; reelin antibody; RELN antibody
  • Isotype
    Rabbit IgG
  • Preparation
    This antibody was obtained by immunization of Peptide (Accession Number: NM_005045). Purification method: Antigen affinity purified.
  • Clonality
    Polyclonal
  • Formulation
    PBS with 0.1% sodium azide and 50% glycerol pH 7.3.
  • Storage instructions
    Store at -20℃. DO NOT ALIQUOT
  • Applications

    Recommended Dilution:

    IHC: 1:20-1:200

  • Validations

    Immunohistochemistry of paraffin-embedded human liver slide using Catalog No:114685(RELN Antibody) at dilution of 1:50(under 10x lens)

    Immunohistochemistry of paraffin-embedded human liver slide using Catalog No:114685(RELN Antibody) at dilution of 1:50(under 10x lens)

    Immunohistochemistry of paraffin-embedded human liver slide using Catalog No:114685(RELN Antibody) at dilution of 1:50(under 40x lens)

    Immunohistochemistry of paraffin-embedded human liver slide using Catalog No:114685(RELN Antibody) at dilution of 1:50(under 40x lens)

  • Background
    RELN belongs to the reelin family. It is an extracellular matrix serine protease that plays a role in layering of neurons in the cerebral cortex and cerebellum. It is a secreted glycoprotein which is essential for neuronal migration in the cortex. RELN regulates microtubule function in neurons and neuronal migration. It affects migration of sympathetic preganglionic neurons in the spinal cord, where it seems to act as a barrier to neuronal migration. Enzymatic activity is important for the modulation of cell adhesion. Binding to the extracellular domains of lipoprotein receptors VLDLR and ApoER2, RELN induces tyrosine phosphorylation of Dab1 and modulation of Tau phosphorylation. Defects in RELN are the cause of lissencephaly type 2 (LIS2).

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"