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OFD1 Antikörper (AA 136-387 of Human)

OFD1 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN1886022
  • Target Alle OFD1 Antikörper anzeigen
    OFD1 (Oral-Facial-Digital Syndrome 1 (OFD1))
    Bindungsspezifität
    • 6
    • 2
    • 1
    • 1
    • 1
    • 1
    AA 136-387 of Human
    Reaktivität
    • 13
    • 4
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    Human
    Wirt
    • 13
    Kaninchen
    Klonalität
    • 13
    Polyklonal
    Konjugat
    • 9
    • 2
    • 1
    • 1
    Dieser OFD1 Antikörper ist unkonjugiert
    Applikation
    • 8
    • 5
    • 3
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    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
    Top Product
    Discover our top product OFD1 Primärantikörper
  • 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 (OFD1 Produkte)
    Synonyme
    71-7A antikoerper, CXorf5 antikoerper, JBTS10 antikoerper, RP23 antikoerper, SGBS2 antikoerper, RGD1562231 antikoerper, OFD1, centriole and centriolar satellite protein antikoerper, OFD1 antikoerper, ofd1 antikoerper, Ofd1 antikoerper
    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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