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FoxD3 Polyclonal Antibody
Datasheet   

  • Catalog Number:

    E20-71743
  • Amount:

    100ul
  • Molecular Weight:

    47630Da
  • Applications:

    WB;IHC-p;IF(paraffin section);ELISA
  • Reactivity:

    Human;Mouse
  • Purification:

    The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
  • Immunogen:

    The antiserum was produced against synthesized peptide derived from human FOXD3. AA range:211-260
  • Source:

    Polyclonal, Rabbit,IgG
  • Western Blot analysis of various cells using FoxD3 Polyclonal Antibody cells nucleus extracted by Minute TM Cytoplasmic and Nuclear Fractionation kit
  • Gene Name:

    FOXD3
  • Dilution:

    Western Blot: 1/500 - 1/2000. Immunohistochemistry: 1/100 - 1/300. ELISA: 1/5000. Not yet tested in other applications.
  • Protein Name:

    Forkhead box protein D3
  • Human Gene Id:

    27022
  • Human Swiss Prot No:

    Q9UJU5
  • Mouse Gene Id:

    15221
  • Mouse Swiss Prot No:

    Q61060
  • Specificity:

    FoxD3 Polyclonal Antibody detects endogenous levels of FoxD3 protein.
  • Formulation:

    Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
  • Concentration:

    1 mg/ml
  • Storage Stability:

    -20°C/1 year
  • Other Name:

    FOXD3; HFH2; Forkhead box protein D3; HNF3/FH transcription factor genesis
  • Observed Band(KD):

    48
  • Background:

    forkhead box D3(FOXD3) Homo sapiens 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.

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Catalog Number

  • Amount:100ul
  • Price:225$

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AbPromise
FoxD3 Polyclonal Antibody | EnoGene Biotech Co. Ltd