Phone:
+1 877 302 8632
Fax:
+1 888 205 9894 (Toll-free)
E-Mail:
orders@antibodies-online.com

HMX1 antibody (Middle Region)

HMX1 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1107589
  • Target See all HMX1 products
    HMX1 (H6 Family Homeobox 1 (HMX1))
    Binding Specificity
    • 2
    • 1
    • 1
    Middle Region
    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)
    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 (HMX1 Products)
    Synonyms
    GH6 antibody, H6 antibody, NKX5-3 antibody, Nkx5-3 antibody, im:7155045 antibody, zgc:172164 antibody, H6 family homeobox 1 antibody, H6 homeobox 1 antibody, HMX1 antibody, Hmx1 antibody, hmx1 antibody
    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
You are here:
Support