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HMX1 antibody (Middle Region)

This Rabbit Polyclonal antibody specifically detects HMX1 in WB. It exhibits reactivity toward Human.
Catalog No. ABIN1107589

Quick Overview for HMX1 antibody (Middle Region) (ABIN1107589)

Target

HMX1 (H6 Family Homeobox 1 (HMX1))

Reactivity

  • 5
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 4
  • 1
Rabbit

Clonality

  • 5
Polyclonal

Conjugate

  • 5
This HMX1 antibody is un-conjugated

Application

  • 5
  • 1
Western Blotting (WB)
  • Binding Specificity

    • 2
    • 1
    • 1
    Middle Region

    Sequence

    AGETRGGVGV GGGRKKKTRT VFSRSQVFQL ESTFDLKRYL STAERAGLAA

    Cross-Reactivity (Details)

    Species reactivity (expected):Mouse, Rat, Dog, Chicken, Bovine, Drosophila, ZebrafishSpecies reactivity (tested):Human

    Purification

    Purified using Protein A affinity column

    Immunogen

    The immunogen for anti-HMX1 antibody: synthetic peptide directed towards the middle region of human HMX1.

    Isotype

    IgG
  • Application Notes

    Optimal working dilution should be determined by the investigator.

    Restrictions

    For Research Use only
  • Reconstitution

    Add 100 μL of distilled water to a final concentration of 1 mg/mL.

    Handling Advice

    Avoid repeated freezing and thawing.

    Storage

    4 °C/-20 °C

    Storage Comment

    Store lyophilized at 2-8 °C or at -20 °C long term. After reconstitution store the antibody undiluted at 2-8 °C for up to one month or in aliquots at -20 °C long term.
  • Target

    HMX1 (H6 Family Homeobox 1 (HMX1))

    Alternative Name

    HMX1

    Background

    HMX1 acts as a transcriptional antagonist and is part of the Hmx family of homeodomain proteins which are predominately expressed in discrete regions of developing sensory tissues. Defects in HMX1 are the cause of oculoauricular syndrome (OCLAUS) also known as microphthalmia, microcornea, anterior segment dysgenesis, cataract, ocular coloboma, retinal pigment epithelium abnormalities, rod-cone dystrophy, and anomalies of the external ear.Synonyms: Homeobox protein H6, Homeobox protein HMX-1

    Gene ID

    3166

    NCBI Accession

    NP_061815
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