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AHI1 antibody (AA 1-12)

AHI1 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN1885582
  • Target See all AHI1 Antibodies
    AHI1 (Abelson Helper Integration Site 1 (AHI1))
    Binding Specificity
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-12
    Reactivity
    • 26
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Host
    • 23
    • 4
    • 1
    Rabbit
    Clonality
    • 26
    • 2
    Polyclonal
    Conjugate
    • 19
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This AHI1 antibody is un-conjugated
    Application
    • 17
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Purified by antigen-affinity chromatography.
    Immunogen
    Synthetic peptide contain a sequence corresponding to a region within amino acids 1 and 12 of Jouberin
    Top Product
    Discover our top product AHI1 Primary Antibody
  • Application Notes
    Suggested dilutions:
    Western blotting: 1.500-1.3000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.
    Preservative
    Thimerosal (Merthiolate)
    Precaution of Use
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Storage
    4 °C/-20 °C
    Storage Comment
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target
    AHI1 (Abelson Helper Integration Site 1 (AHI1))
    Alternative Name
    Jouberin (AHI1 Products)
    Synonyms
    AHI1 antibody, AHI-1 antibody, JBTS3 antibody, ORF1 antibody, dJ71N10.1 antibody, 1700015F03Rik antibody, Ahi-1 antibody, D10Bwg0629e antibody, Abelson helper integration site 1 antibody, AHI1 antibody, ahi1 antibody, Ahi1 antibody
    Background
    This gene is apparently required for both cerebellar and cortical development in humans.This gene mutations cause specific forms of Joubert syndrome-related disorders.Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci.Alternatively spliced transcript variants encoding different isoforms have been identified.[provided by RefSeq]
    Synonyms: ORF1, AHI-1, JBTS3, FLJ14023, FLJ20069, dJ71N10.1, DKFZp686J1653
    Molecular Weight
    137 kDa
    Gene ID
    54806
    NCBI Accession
    NP_060121, NM_017651
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