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GTF2I Antikörper

Dieses Anti-GTF2I-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von GTF2I in WB, IHC und ELISA. Geeignet für Human, Maus und Hund.
Produktnummer ABIN2460315

Kurzübersicht für GTF2I Antikörper (ABIN2460315)

Target

Alle GTF2I Antikörper anzeigen
GTF2I (General Transcription Factor III (GTF2I))

Reaktivität

  • 53
  • 25
  • 20
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
Human, Maus, Hund

Wirt

  • 48
  • 5
Kaninchen

Klonalität

  • 48
  • 5
Polyklonal

Konjugat

  • 36
  • 3
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser GTF2I Antikörper ist unkonjugiert

Applikation

  • 41
  • 22
  • 16
  • 15
  • 8
  • 5
  • 3
  • 2
  • 2
  • 2
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), ELISA
  • Aufreinigung

    Antibody is purified by peptide affinity chromatography method.

    Immunogen

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GTF2I.
  • Applikationshinweise

    GTF2I antibody can be used for detection of GTF2I by ELISA at 1:62500. GTF2I antibody can be used for detection of GTF2I by western blot at 0.5 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Lyophilized

    Rekonstitution

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    Konzentration

    1 mg/mL

    Buffer

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    Handhabung

    As with any antibody avoid repeat freeze-thaw cycles.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store GTF2I antibody at -20 °C.
  • Target

    GTF2I (General Transcription Factor III (GTF2I))

    Andere Bezeichnung

    GTF2I

    Hintergrund

    GTF2I encodes a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23. The exon (s) encoding 5' UTR has not been fully defined, but this gene is known to contain at least 34 exons, and its alternative splicing generates 4 transcript variants.

    Molekulargewicht

    110 kDa

    Gen-ID

    2969

    NCBI Accession

    NP_127493

    UniProt

    Q75M86
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