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T-Box 1 Antikörper (Middle Region)

TBX1 Reaktivität: Human, Maus, Ratte, Meerschweinchen, Kaninchen, Pferd WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN2777911
  • Target Alle T-Box 1 (TBX1) Antikörper anzeigen
    T-Box 1 (TBX1)
    Bindungsspezifität
    • 16
    • 13
    • 8
    • 6
    • 5
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Middle Region
    Reaktivität
    Human, Maus, Ratte, Meerschweinchen, Kaninchen, Pferd
    Wirt
    • 51
    • 2
    • 1
    Kaninchen
    Klonalität
    • 52
    • 2
    Polyklonal
    Konjugat
    • 24
    • 5
    • 4
    • 4
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser T-Box 1 Antikörper ist unkonjugiert
    Applikation
    • 48
    • 25
    • 21
    • 19
    • 14
    • 6
    • 5
    • 2
    • 1
    • 1
    Western Blotting (WB)
    Sequenz
    PVASPTQPSG TEKGGHVLKD KEVKAETSRN TPEREVELLR DAGGCVNLGL
    Homologie
    Guinea Pig: 85%, Horse: 77%, Human: 100%, Mouse: 77%, Rabbit: 85%, Rat: 85%
    Produktmerkmale
    This is a rabbit polyclonal antibody against TBX1. It was validated on Western Blot using a cell lysate as a positive control.
    Aufreinigung
    Affinity Purified
    Immunogen
    The immunogen is a synthetic peptide directed towards the middle region of human TBX1
    Top Product
    Discover our top product TBX1 Primärantikörper
  • Applikationshinweise
    Optimal working dilutions should be determined experimentally by the investigator.
    Kommentare

    Antigen size: 398 AA

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Format
    Liquid
    Konzentration
    Lot specific
    Buffer
    Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Handhabung
    Avoid repeated freeze-thaw cycles.
    Lagerung
    -20 °C
    Informationen zur Lagerung
    For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
  • Target
    T-Box 1 (TBX1)
    Andere Bezeichnung
    TBX1 (TBX1 Produkte)
    Synonyme
    CAFS antikoerper, CTHM antikoerper, DGCR antikoerper, DGS antikoerper, DORV antikoerper, TBX1C antikoerper, TGA antikoerper, VCFS antikoerper, mp:zf637-3-000616 antikoerper, zgc:136724 antikoerper, TBX1 antikoerper, dgs antikoerper, tga antikoerper, cafs antikoerper, cthm antikoerper, dgcr antikoerper, dorv antikoerper, vcfs antikoerper, tbx1c antikoerper, xtbx1 antikoerper, tbx1 antikoerper, T-box 1 antikoerper, T-box 1 S homeolog antikoerper, T-box 1 L homeolog antikoerper, TBX1 antikoerper, Tbx1 antikoerper, tbx1 antikoerper, tbx1.S antikoerper, tbx1.L antikoerper
    Hintergrund
    TBX1 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. TBX1 product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where TBX1 has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene. This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. This gene product shares 98 % amino acid sequence identity with the mouse ortholog. DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped. Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.
    Alias Symbols: CAFS, CTHM, DGCR, DGS, DORV, TBX1C, TGA, VCFS
    Protein Interaction Partner: TERF2, TERF1,
    Protein Size: 398
    Molekulargewicht
    43 kDa
    Gen-ID
    6899
    NCBI Accession
    NM_080646, NP_542377
    UniProt
    O43435
    Pathways
    Retinoic Acid Receptor Signaling Pathway, Sensory Perception of Sound, Cellular Response to Molecule of Bacterial Origin, Regulation of Muscle Cell Differentiation
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