FoxD3 Monoclonal Antibody

    • Catalog No.:YM0283
    • Applications:WB;IHC;IF;ELISA
    • Reactivity:Human;Mouse;Monkey
      • Target:
      • FoxD3
      • Gene Name:
      • FOXD3
      • Protein Name:
      • Forkhead box protein D3
      • Human Swiss Prot No:
      • Q9UJU5
      • Mouse Swiss Prot No:
      • Q61060
      • Immunogen:
      • Purified recombinant fragment of human FoxD3 expressed in E. Coli.
      • Specificity:
      • FoxD3 Monoclonal Antibody detects endogenous levels of FoxD3 protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Monoclonal, Mouse
      • Dilution:
      • WB 1:500 - 1:2000. IHC 1:200 - 1:1000. ELISA: 1:10000.. IF 1:50-200
      • Purification:
      • Affinity purification
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • FOXD3;HFH2;Forkhead box protein D3;HNF3/FH transcription factor genesis
      • Molecular Weight(Da):
      • 48kD
      • References:
      • 1. J Neuroimmune Pharmacol. 2009 Mar;4(1):103-15.
        2. Nature. 2006 May 18;441(7091):315-21.
      • Background:
      • This gene belongs to the forkhead family of transcription factors which is characterized by a distinct forkhead domain. Mutations in this gene cause autoimmune susceptibility 1. [provided by RefSeq, Nov 2008],
      • Function:
      • disease:Defects in FOXD3 are associated with susceptibility to autoimmune disease type 1 (AIS1) [MIM:607836]; also called vitiligo-associated multiple autoimmune disease susceptibility type 2 (VAMAS2). Generalized vitiligo is an acquired disorder in which white patches of skin and hair result from autoimmune loss of melanocytes, often associated with other autoimmune disorders. Most cases occur in a sporadic family pattern suggesting polygenic, multifactorial inheritance. However, a striking family in which a somewhat unusual vitiligo phenotype has been described, characterized by progressively coalescent diffuse depigmentation and relatively early disease onset, segregated as an apparent autosomal dominant with incomplete penetrance.,function:Binds to the consensus sequence 5'-A[AT]T[AG]TTTGTTT-3' and acts as a transcriptional repressor. Also acts as a transcriptional activator. Promote
      • Subcellular Location:
      • Nucleus .
      • Expression:
      • Expressed in chronic myeloid leukemia, Jurkat T-cell leukemia and teratocarcinoma cell lines, but not in any other cell lines or normal tissues examined.
      • Products Images
      • Western Blot analysis using FoxD3 Monoclonal Antibody against NTERA-2 (1), HUVE-12 (2), HEK293 (3), HeLa (4), Jurkat (5), K562 (6), RAW264.7 (7), NIH/3T3 (8), and COS7 (9) cell lysate.
      • Immunohistochemistry analysis of paraffin-embedded lung cancer tissues (left) and ovarian cancer tissues (right) with DAB staining using FoxD3 Monoclonal Antibody.