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AHI1 anticorps (AA 1-12)

AHI1 Reactivité: Humain WB Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1885582
  • Antigène Voir toutes AHI1 Anticorps
    AHI1 (Abelson Helper Integration Site 1 (AHI1))
    Épitope
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 1-12
    Reactivité
    • 26
    • 6
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 23
    • 4
    • 1
    Lapin
    Clonalité
    • 26
    • 2
    Polyclonal
    Conjugué
    • 19
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp AHI1 est non-conjugé
    Application
    • 17
    • 7
    • 5
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purification
    Purified by antigen-affinity chromatography.
    Immunogène
    Synthetic peptide contain a sequence corresponding to a region within amino acids 1 and 12 of Jouberin
    Top Product
    Discover our top product AHI1 Anticorps primaire
  • Indications d'application
    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.
    Agent conservateur
    Thimerosal (Merthiolate)
    Précaution d'utilisation
    Biohazard Informations: This product contains thimerosal which is hazardous.
    Stock
    4 °C/-20 °C
    Stockage commentaire
    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Antigène
    AHI1 (Abelson Helper Integration Site 1 (AHI1))
    Autre désignation
    Jouberin (AHI1 Produits)
    Synonymes
    anticorps AHI1, anticorps AHI-1, anticorps JBTS3, anticorps ORF1, anticorps dJ71N10.1, anticorps 1700015F03Rik, anticorps Ahi-1, anticorps D10Bwg0629e, anticorps Abelson helper integration site 1, anticorps AHI1, anticorps ahi1, anticorps Ahi1
    Sujet
    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
    Poids moléculaire
    137 kDa
    ID gène
    54806
    NCBI Accession
    NP_060121, NM_017651
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