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ZNF703 antibody

The Rabbit Polyclonal anti-ZNF703 antibody has been validated for ELISA and IHC. It is suitable to detect ZNF703 in samples from Human and Mouse.
Catalog No. ABIN7248233

Quick Overview for ZNF703 antibody (ABIN7248233)

Target

See all ZNF703 Antibodies
ZNF703 (Zinc Finger Protein 703 (ZNF703))

Reactivity

  • 47
  • 7
  • 6
  • 6
  • 5
  • 5
  • 3
  • 3
  • 2
  • 1
  • 1
  • 1
Human, Mouse

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

  • 36
  • 17
  • 13
  • 13
  • 3
  • 3
  • 3
  • 3
  • 3
  • 2
  • 1
ELISA, Immunohistochemistry (IHC)
  • Characteristics

    Polyclonal Antibody

    Purification

    Antigen affinity purification

    Immunogen

    Synthetic peptide of human ZNF703

    Isotype

    IgG
  • Application Notes

    IHC 1:30-1:150, ELISA 1:5000-1:10000

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1.2 mg/mL

    Buffer

    PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

    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

    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.

    UniProt

    Q9H7S9

    Pathways

    Cell-Cell Junction Organization
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