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MID1 Antikörper (C-Term)

Der Kaninchen Polyklonal Anti-MID1-Antikörper wurde für WB validiert. Er ist geeignet, MID1 in Proben von Human zu detektieren.
Produktnummer ABIN2798159

Kurzübersicht für MID1 Antikörper (C-Term) (ABIN2798159)

Target

Alle MID1 Antikörper anzeigen
MID1 (Midline 1 (MID1))

Reaktivität

  • 47
  • 35
  • 31
  • 6
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Human

Wirt

  • 49
  • 2
Kaninchen

Klonalität

  • 50
  • 1
Polyklonal

Konjugat

  • 26
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser MID1 Antikörper ist unkonjugiert

Applikation

  • 44
  • 16
  • 13
  • 11
  • 6
  • 6
  • 4
  • 3
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

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

    Verwendungszweck

    Rabbit Anti-Human MID1 (C-term) Antibody

    Immunogen

    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.

    Isotyp

    Ig Fraction
  • Applikationshinweise

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

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Konzentration

    0.5 mg/mL

    Lagerung

    4 °C,-20 °C

    Informationen zur Lagerung

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

    MID1 (Midline 1 (MID1))

    Andere Bezeichnung

    MID1

    Hintergrund

    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

    Molekulargewicht

    75251 Da

    Gen-ID

    4281

    UniProt

    O15344
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