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OFD1 Antikörper (AA 136-387 of Human)

Dieses Anti-OFD1-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von OFD1 in WB. Geeignet für Human.
Produktnummer ABIN1886022

Kurzübersicht für OFD1 Antikörper (AA 136-387 of Human) (ABIN1886022)

Target

Alle OFD1 Antikörper anzeigen
OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

Reaktivität

  • 15
  • 5
  • 4
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
Human

Wirt

  • 15
Kaninchen

Klonalität

  • 15
Polyklonal

Konjugat

  • 11
  • 2
  • 1
  • 1
Dieser OFD1 Antikörper ist unkonjugiert

Applikation

  • 11
  • 7
  • 4
  • 3
  • 2
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB)
  • Bindungsspezifität

    • 7
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 136-387 of Human

    Aufreinigung

    Purified by antigen-affinity chromatography.

    Immunogen

    Recombinant protein fragment contain a sequence corresponding to a region within amino acids 136 and 387 of Human OFD1
  • Applikationshinweise

    Suggested dilutions:
    Western blotting: 1.500-1.3000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    0.1 M Tris-buffered saline with 10 % Glycerol (pH 7.0).0.01 % Thimerosal was added as a preservative.

    Konservierungsmittel

    Thimerosal (Merthiolate)

    Vorsichtsmaßnahmen

    Biohazard Informations: This product contains thimerosal which is hazardous.

    Lagerung

    4 °C/-20 °C

    Informationen zur Lagerung

    Store at -20 °C for long term preservation (recommended). Store at 4 °C for short term use.
  • Target

    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))

    Andere Bezeichnung

    oral-facial-digital syndrome 1

    Hintergrund

    This gene is located on the X chromosome and encodes a centrosomal protein.A knockout mouse model has been used to study the effect of mutations in this gene.The mouse gene is also located on the X chromosome, however, unlike the human gene it is not subject to X inactivation.Mutations in this gene are associated with oral-facial-digital syndrome type I and Simpson-Golabi-Behmel syndrome type 2.Many pseudogenes have been identified, a single pseudogene is found on chromosome 5 while as many as fifteen have been found on the Y chromosome.Alternatively spliced transcripts have been described for this gene but the biological validity of these transcripts has not been determined.[provided by RefSeq]

    Molekulargewicht

    117 kDa

    Gen-ID

    8481

    NCBI Accession

    NM_003611, NP_003602

    Pathways

    M Phase
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