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WHSC1 antibody (AA 525-575)

WHSC1 Reactivity: Human WB Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7453147
  • Target See all WHSC1 Antibodies
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    Binding Specificity
    • 5
    • 3
    • 3
    • 1
    • 1
    AA 525-575
    Reactivity
    • 21
    • 5
    • 2
    • 2
    • 2
    • 2
    • 2
    • 2
    • 1
    Human
    Host
    • 18
    • 3
    Rabbit
    Clonality
    • 20
    • 1
    Polyclonal
    Conjugate
    • 11
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WHSC1 antibody is un-conjugated
    Application
    • 9
    • 5
    • 4
    • 4
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Purpose
    Rabbit anti-NSD2 Antibody, Affinity Purified
    Purification
    Affinity Purified
    Immunogen
    between AA 525 and 575
    Isotype
    IgG
    Top Product
    Discover our top product WHSC1 Primary Antibody
  • Application Notes

    IP: Not recommended

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

    Restrictions
    For Research Use only
  • Concentration
    200 μg/mL
    Buffer
    Tris-buffered Saline containing 0.1 % BSA and 0.09 % Sodium Azide
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C
    Expiry Date
    12 months
  • Target
    WHSC1 (Wolf-Hirschhorn Syndrome Candidate 1 (WHSC1))
    Alternative Name
    NSD2 (WHSC1 Products)
    Background
    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].
    Gene ID
    7468
    NCBI Accession
    NP_579877
    UniProt
    O96028
    Pathways
    SARS-CoV-2 Protein Interactome
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