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MID1 anticorps (C-Term)

L’anticorps Lapin Polyclonal anti-MID1 a été validé pour WB. Il convient pour détecter MID1 dans des échantillons de Humain.
N° du produit ABIN2798159

Aperçu rapide pour MID1 anticorps (C-Term) (ABIN2798159)

Antigène

Voir toutes MID1 Anticorps
MID1 (Midline 1 (MID1))

Reactivité

  • 47
  • 33
  • 31
  • 6
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Humain

Hôte

  • 47
  • 2
Lapin

Clonalité

  • 48
  • 1
Polyclonal

Conjugué

  • 24
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Cet anticorp MID1 est non-conjugé

Application

  • 42
  • 16
  • 13
  • 9
  • 6
  • 4
  • 3
  • 2
  • 1
  • 1
Western Blotting (WB)
  • Épitope

    • 15
    • 9
    • 5
    • 4
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 575-603, C-Term

    Fonction

    Rabbit Anti-Human MID1 (C-term) Antibody

    Immunogène

    This MID1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 575-603 amino acids from the C-terminal region of human MID1.

    Isotype

    Ig Fraction
  • Indications d'application

    Western Blot
    Recommended Dilutions
    WB: 1:1000MID1 Antibody (C-term) .

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    0.5 mg/mL

    Stock

    4 °C,-20 °C

    Stockage commentaire

    2-8°C (short-term), -20°C (long-term)
  • Antigène

    MID1 (Midline 1 (MID1))

    Autre désignation

    MID1

    Sujet

    Target Description: The protein encoded by this gene is a member of the tripartite motif (TRIM) family, also known as the 'RING-B box-coiled coil' (RBCC) subgroup of RING finger proteins. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein forms homodimers which associate with microtubules in the cytoplasm. The protein is likely involved in the formation of multiprotein structures acting as anchor points to microtubules. Mutations in this gene have been associated with the X-linked form of Opitz syndrome, which is characterized by midline abnormalities such as cleft lip, laryngeal cleft, heart defects, hypospadias, and agenesis of the corpus callosum. This gene was also the first example of a gene subject to X inactivation in human while escaping it in mouse. Multiple different transcript variants are generated by alternate splicing, however, the full-length nature of some of the variants has not been determined.

    Gene Symbol: MID1

    Poids moléculaire

    75251 Da

    ID gène

    4281

    UniProt

    O15344
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