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ADD1 (Phospho-Ser726) Antibody

Catalog No : A0002
  • Applications
    WB, IHC, IF, ELISA
  • Reactivity
    Human, Mouse, Rat
  • Application Dilutions
    WB: 1:500~1:1000 IHC: 1:50~1:100 IF: 1:100~1:500 ELISA: 1:40000
  • Size
    50ul
  • Price
    $175.00
Details
  • Product Name
    ADD1 (Phospho-Ser726) Antibody
  • Catalog No
    A0002
  • Storage/Stability
    Stable at -20°C for at least 1 year.
  • Applications
    WB, IHC, IF, ELISA
  • Clonality
    Polyclonal
  • Source
    Rabbit
  • Reactivity
    Human, Mouse, Rat
  • Application Dilutions
    WB: 1:500~1:1000 IHC: 1:50~1:100 IF: 1:100~1:500 ELISA: 1:40000
  • Database Links
    Gene ID: 118/119, Swiss-Prot #: P35611/P35612, OMIM #: 102680/102681, Unigene #: Hs.183706/Hs.701490/Hs.188528
  • Image 1
    Immunofluorescence analysis of HeLa cells, using ADD1 (Phospho-Ser726) Antibody. The picture on the right is blocked with the phospho peptide.
  • Image 2
    Immunohistochemistry analysis of paraffin-embedded human breast carcinoma, using ADD1 (Phospho-Ser726) Antibody. The picture on the right is blocked with the phospho peptide.
  • Immunogen
    The antiserum was produced against synthesized peptide derived from human ADD1 around the phosphorylation site of Ser726.
  • Immunogen Range
    688-737
  • Modification Sites
    H: S726/S713 M: S724/S712 R: S724/S712
  • MW
    80 kDa
  • NCBI Gene Symbol
    ADD1
  • Physical Form
    Rabbit IgG in phosphate buffered saline (without Mg2+ and Ca2+), pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol.
  • Purification
    The antibody was purified from rabbit antiserum by affinity-chromatography using phospho peptide. The antibody against non-phospho peptide was removed by chromatography using corresponding non-phospho peptide.
  • Specificity
    ADD1 (Phospho-Ser726) Antibody detects endogenous levels of ADD1 only when phosphorylated at Ser726.
  • Synonyms
    Alpha-adducin, Erythrocyte adducin subunit alpha , ADD1 , ADDA
  • Target Modification
    Phospho
Application Images
Image 1 Immunofluorescence analysis of HeLa cells, using ADD1 (Phospho-Ser726) Antibody. The picture on the right is blocked with the phospho peptide.
Image 2 Immunohistochemistry analysis of paraffin-embedded human breast carcinoma, using ADD1 (Phospho-Ser726) Antibody. The picture on the right is blocked with the phospho peptide.
Image 3 Western blot analysis of lysates from HeLa cells treated with Forskolin 40nM 30', using ADD1 (Phospho-Ser726) Antibody. The lane on the right is blocked with the phospho peptide.
  • Xiang, F., Neal, P.: Efficient MCMC for temporal epidemics via parameter reduction. Comput. Stat. Data Anal.
  • Xiang, F., Neal, P.: Efficient MCMC for temporal epidemics via parameter reduction. Comput. Stat. Data Anal.
  • Xiang, F., Neal, P.: Efficient MCMC for temporal epidemics via parameter reduction. Comput. Stat. Data Anal.
  • Xiang, F., Neal, P.: Efficient MCMC for temporal epidemics via parameter reduction. Comput. Stat. Data Anal.
  • Xiang, F., Neal, P.: Efficient MCMC for temporal epidemics via parameter reduction. Comput. Stat. Data Anal.
For the process of attaching edges to nodes, it is straightforward to compute the likelihood using (2). However, because of the nature of weighted sampling without replacement, we have to, for each i, calculate the probability conditi onal on each of the Xi!Xi! permutations of the selected nodes and then aver age over all Xi!Xi! probabilities to arrive at the likelihood. As calculating the exact likelihood in this way is not computationally feasible because the factorial grows faster than the exponential function, we approximate the likelihood based on one permutation of weighted sampling without replacement instead. The contribution by the new edges brought by node i is
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