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MID1 Antikörper (AA 226-278)

Der Kaninchen Polyklonal anti-MID1 Antikörper wird verwendet zum Nachweis von MID1 in Proben von Human und Maus. Er wurde validiert für WB, ELISA, IF, IHC (p) und FACS.
Produktnummer ABIN7872405
644,88 €
Zzgl. Versandkosten 20,00 € und MwSt
100 μg
Lieferung nach: Deutschland
Lieferung in 6 bis 9 Werktagen

Kurzübersicht für MID1 Antikörper (AA 226-278) (ABIN7872405)

Target

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

Reaktivität

  • 49
  • 34
  • 32
  • 6
  • 5
  • 5
  • 5
  • 5
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
Human, Maus

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
  • 17
  • 13
  • 10
  • 7
  • 4
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA, Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Flow Cytometry (FACS)
  • Bindungsspezifität

    • 15
    • 10
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 226-278

    Verwendungszweck

    MID1 Antibody

    Aufreinigung

    Affinity purified

    Immunogen

    Amino acids N226-Q278 from the human protein were used as the immunogen for the MID1 antibody.

    Isotyp

    IgG
  • Applikationshinweise

    Optimal dilution of the MID1 antibody should be determined by the researcher.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Buffer

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    Lagerung

    -20 °C

    Informationen zur Lagerung

    Store the MID1 antibody at -20oC.
  • Target

    MID1 (Midline 1 (MID1))

    Andere Bezeichnung

    MID1

    Hintergrund

    Midline-1 is a protein found in humans that is encoded by the MID1 gene. 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. Alternative promoter use, alternative splicing and alternative polyadenylation result in multiple transcript variants that have different tissue specificities.

    UniProt

    O15344
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