ATN1 antibody

Cat.#: 108334

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Product Information

  • Product Name
    ATN1 antibody
  • Documents
  • Description
    ATN1 Rabbit Polyclonal antibody. Positive IHC detected in human ovary tissue, human testis tissue. Positive WB detected in mouse testis tissue. Observed molecular weight by Western-blot: 105-110 kDa
  • Tested applications
    ELISA, WB, IHC
  • Species reactivity
    Human, Mouse; other species not tested.
  • Alternative names
    ATN1 antibody; atrophin 1 antibody; B37 antibody; D12S755E antibody; DRPLA antibody; HRS antibody; NOD antibody
  • Isotype
    Rabbit IgG
  • Preparation
    This antibody was obtained by immunization of ATN1 recombinant protein (Accession Number: NM_001940). 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:

    WB: 1:200-1:1000

    IHC: 1:20-1:200

  • Validations

    mouse testis tissue were subjected to SDS PAGE followed by western blot with Catalog No:108334(ATN1 Antibody) at dilution of 1:300

    mouse testis tissue were subjected to SDS PAGE followed by western blot with Catalog No:108334(ATN1 Antibody) at dilution of 1:300

    Immunohistochemistry of paraffin-embedded human ovary tissue slide using Catalog No:108334(ATN1 Antibody) at dilution of 1:50 (under 10x lens)

    Immunohistochemistry of paraffin-embedded human ovary tissue slide using Catalog No:108334(ATN1 Antibody) at dilution of 1:50 (under 10x lens)

    Immunohistochemistry of paraffin-embedded human ovary tissue slide using Catalog No:108334(ATN1 Antibody) at dilution of 1:50 (under 40x lens)

    Immunohistochemistry of paraffin-embedded human ovary tissue slide using Catalog No:108334(ATN1 Antibody) at dilution of 1:50 (under 40x lens)

  • Background
    ATN1 also known as Atrophin-1 is a protein that in humans is encoded by the ATN1 gene. Dentatorubral pallidoluysian atrophy is a rare neurodegenerative disorder characterized by cerebellar ataxia, myoclonic epilepsy, choreoathetosis, and dementia. The disorder is related to the expansion of a trinucleotide repeat within this gene. The encoded protein includes a serine repeat and a region of alternating acidic and basic amino acids, as well as the variable glutamine repeat.

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