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MID1 anticorps (AA 200-250)

MID1 Reactivité: Humain, Souris, Rat WB, IF (p), IHC (p) Hôte: Lapin Polyclonal unconjugated
N° du produit ABIN1387054
  • Antigène Voir toutes MID1 Anticorps
    MID1 (Midline 1 (MID1))
    Épitope
    • 14
    • 10
    • 10
    • 6
    • 5
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 200-250
    Reactivité
    • 49
    • 27
    • 26
    • 6
    • 5
    • 5
    • 5
    • 5
    • 3
    • 3
    • 2
    • 2
    • 2
    • 1
    Humain, Souris, Rat
    Hôte
    • 48
    • 2
    Lapin
    Clonalité
    • 49
    • 1
    Polyclonal
    Conjugué
    • 26
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp MID1 est non-conjugé
    Application
    • 49
    • 21
    • 12
    • 8
    • 7
    • 4
    • 2
    • 1
    Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
     Réactivité croisée
    Humain, Souris, Rat
    Purification
    Purified by Protein A.
    Immunogène
    KLH conjugated synthetic peptide derived from human Midline-1/RNF59
    Isotype
    IgG
    Top Product
    Discover our top product MID1 Anticorps primaire
  • Indications d'application
    WB 1:300-5000
    IHC-P 1:200-400
    IF(IHC-P) 1:50-200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 μg/μL
    Buffer
    0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
    Agent conservateur
    ProClin
    Précaution d'utilisation
    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Stockage commentaire
    Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
    Date de péremption
    12 months
  • Antigène
    MID1 (Midline 1 (MID1))
    Autre désignation
    Midline-1 (MID1 Produits)
    Synonymes
    anticorps BBBG1, anticorps FXY, anticorps GBBB1, anticorps MIDIN, anticorps OGS1, anticorps OS, anticorps OSX, anticorps RNF59, anticorps TRIM18, anticorps XPRF, anticorps ZNFXY, anticorps 61B3-R, anticorps DXHXS1141, anticorps Fxy, anticorps Trim18, anticorps Midline1, anticorps bbbg1, anticorps fxy, anticorps gbbb1, anticorps midin, anticorps ogs1, anticorps osx, anticorps rnf59, anticorps trim18, anticorps xprf, anticorps znfxy, anticorps midline 1, anticorps midline 1 L homeolog, anticorps MID1, anticorps Mid1, anticorps mid1, anticorps mid1.L
    Sujet

    Synonyms: BBBG1, Finger on X and Y mouse homolog of antibody, FXY, GBBB1, MID-1, Mid1, Midin, Midline 1 Opitz/BBB syndrome, Midline 1, Midline 1 ring finger, Midline 1 RING finger protein, Midline-1, Midline1, OGS1, OSX, Putative transcription factor XPRF, RING finger protein 59, RNF59, TRI18, TRI18_HUMAN, TRIM18, Tripartite mot containing protein 18, Tripartite mot protein TRIM18, Tripartite mot-containing protein 18, XPRF, Zinc finger X and Y antibody, ZNFXY.

    Background: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.

    ID gène
    4281
    UniProt
    O15344
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