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ASXL1 antibody

The Rabbit Polyclonal anti-ASXL1 antibody has been validated for WB. It is suitable to detect ASXL1 in samples from Human and Mouse.
Catalog No. ABIN5647693

Quick Overview for ASXL1 antibody (ABIN5647693)

Target

See all ASXL1 Antibodies
ASXL1 (Additional Sex Combs Like 1 (ASXL1))

Reactivity

  • 26
  • 23
  • 1
Human, Mouse

Host

  • 26
  • 3
Rabbit

Clonality

  • 26
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Polyclonal

Conjugate

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  • 2
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  • 1
  • 1
  • 1
  • 1
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  • 1
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  • 1
  • 1
This ASXL1 antibody is un-conjugated

Application

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Western Blotting (WB)
  • Purification

    Antigen affinity purified

    Immunogen

    Amino acids KKERTWAEAARLVLENYSDAPMTPKQILQVIEAE were used as the immunogen for the ASXL1 antibody.

    Isotype

    IgG
  • Application Notes

    Optimal dilution of the ASXL1 antibody should be determined by the researcher.\. Western Blot: 0.5-1 μg/mL

    Restrictions

    For Research Use only
  • Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Storage

    -20 °C

    Storage Comment

    After reconstitution, the ASXL1 antibody can be stored for up to one month at 4°C. For long-term, aliquot and store at -20°C. Avoid repeated freezing and thawing.
  • Target

    ASXL1 (Additional Sex Combs Like 1 (ASXL1))

    Alternative Name

    ASXL1

    Background

    Putative Polycomb group protein ASXL1 is a protein that in humans is encoded by the ASXL1 gene. This gene is similar to the Drosophila additional sex combs gene, which encodes a chromatin-binding protein required for normal determination of segment identity in the developing embryo. The protein is a member of the Polycomb group of proteins, which are necessary for the maintenance of stable repression of homeotic and other loci. The protein is thought to disrupt chromatin in localized areas, enhancing transcription of certain genes while repressing the transcription of other genes. The protein encoded by this gene functions as a ligand-dependent co-activator for retinoic acid receptor in cooperation with nuclear receptor coactivator 1. Mutations in this gene are associated with myelodysplastic syndromes and chronic myelomonocytic leukemia. Alternative splicing results in multiple transcript variants.

    UniProt

    Q8IXJ9

    Pathways

    Retinoic Acid Receptor Signaling Pathway
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