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ZNF703 antibody

ZNF703 Reactivity: Human, Mouse, Rat IHC Host: Rabbit Polyclonal unconjugated
Catalog No. ABIN7257802
  • Target See all ZNF703 Antibodies
    ZNF703 (Zinc Finger Protein 703 (ZNF703))
    Reactivity
    • 47
    • 7
    • 7
    • 6
    • 5
    • 5
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    Human, Mouse, Rat
    Host
    • 44
    • 2
    • 1
    Rabbit
    Clonality
    • 45
    • 2
    Polyclonal
    Conjugate
    • 19
    • 3
    • 3
    • 3
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This ZNF703 antibody is un-conjugated
    Application
    • 35
    • 17
    • 13
    • 13
    • 3
    • 3
    • 3
    • 3
    • 2
    • 2
    • 1
    Immunohistochemistry (IHC)
    Characteristics
    Polyclonal Antibody
    Purification
    Affinity purification
    Immunogen
    Recombinant fusion protein of human ZNF703 (NP_079345.1).
    Isotype
    IgG
  • Application Notes
    IHC 1:50-1:200
    Restrictions
    For Research Use only
  • Format
    Liquid
    Concentration
    1 mg/mL
    Buffer
    PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3
    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
    -20 °C
    Storage Comment
    Store at -20°C. Avoid freeze / thaw cycles.
  • Target
    ZNF703 (Zinc Finger Protein 703 (ZNF703))
    Alternative Name
    ZNF703 (ZNF703 Products)
    Background
    ZNF703 (zinc finger protein 703) is a 590 amino acid nuclear protein that contains one C2H2-type zinc finger and is thought to play a role in transcriptional regulation. Multiple isoforms of ZNF703 exist due to alternative splicing events. The gene encoding ZNF703 maps to human chromosome 8, which consists of nearly 146 million base pairs, houses more than 800 genes and is associated with a variety of diseases and malignancies. Schizophrenia, bipolar disorder, Trisomy 8, Pfeiffer syndrome, congenital hypothyroidism, Waardenburg syndrome and some leukemias and lymphomas are thought to occur as a result of defects in specific genes that map to chromosome 8.
    Gene ID
    80139
    UniProt
    Q9H7S9
    Pathways
    Cell-Cell Junction Organization
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