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WHSC1 Antikörper (AA 525-575)

WHSC1 Reaktivität: Human WB Wirt: Kaninchen Polyclonal unconjugated
Produktnummer ABIN7453147
  • Target Alle WHSC1 Antikörper anzeigen
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    Bindungsspezifität
    • 5
    • 3
    • 3
    • 1
    • 1
    AA 525-575
    Reaktivität
    • 21
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Wirt
    • 18
    • 3
    Kaninchen
    Klonalität
    • 20
    • 1
    Polyklonal
    Konjugat
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Dieser WHSC1 Antikörper ist unkonjugiert
    Applikation
    • 9
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Verwendungszweck
    Rabbit anti-NSD2 Antibody, Affinity Purified
    Aufreinigung
    Affinity Purified
    Immunogen
    between AA 525 and 575
    Isotyp
    IgG
    Top Product
    Discover our top product WHSC1 Primärantikörper
  • Applikationshinweise

    IP: Not recommended

    WB: 1:2,000 - 1:10,000

    Beschränkungen
    Nur für Forschungszwecke einsetzbar
  • Konzentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    Konservierungsmittel
    Sodium azide
    Vorsichtsmaßnahmen
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Lagerung
    4 °C
    Haltbarkeit
    12 months
  • Target
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    Andere Bezeichnung
    NSD2 (WHSC1 Produkte)
    Hintergrund
    Background: MMSET (multiple myeloma SET domain-containing protein) or NSD2 (nuclear SET-domain containing protein 2) is the product of the Wolf-Hirschhorn syndrome candidate 1 (WHSC1) gene. MMSET is a protein that contains four domains present in other developmental proteins: a PWWP domain, an HMG box, a SET domain, and a PHD-type zinc finger. It is expressed ubiquitously in early development and is a probable histone methyltransferase. Wolf-Hirschhorn syndrome (WHS) is a malformation syndrome associated with a hemizygous deletion of the distal short arm of chromosome 4 [taken from NCBI Entrez Gene (Gene ID: 7468].
    Gen-ID
    7468
    NCBI Accession
    NP_579877
    UniProt
    O96028
    Pathways
    SARS-CoV-2 Protein Interaktom
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