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Williams Beuren Syndrome Chromosome Region 22 (WBSCR22) (C-Term) Peptide

WBSCR22 Reactivité: Humain Hôte: Synthetic BP, WB
N° du produit ABIN986133
  • Antigène Tous les produits WBSCR22
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Protein Region
    C-Term
    Origine
    Humain
    Source
    • 1
    Synthetic
    Application
    Blocking Peptide (BP), Western Blotting (WB)
    Séquence
    GGAFERRGIR GHQTRRFPLR MSRRGMVRKS RAWVLEKKER HRRQGREVRP
    Attributs du produit
    This is a synthetic peptide designed for use in combination with anti-WBSCR22 Antibody. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
    Purification
    Purified
  • Indications d'application
    Each Investigator should determine their own optimal working dilution for specific applications.
    Restrictions
    For Research Use only
  • Format
    Lyophilized
    Reconstitution
    Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
    Concentration
    1 mg/mL
    Buffer
    Final peptide concentration is 1 mg/mL in PBS.
    Conseil sur la manipulation
    Avoid repeated freeze-thaw cycles.
    Stock
    -20 °C
    Stockage commentaire
    For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
  • Antigène
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Synonymes
    MGC82375 Peptide, wbmt Peptide, pp3381 Peptide, hussy-3 Peptide, hasj4442 Peptide, zgc:162306 Peptide, HASJ4442 Peptide, HUSSY-3 Peptide, MERM1 Peptide, PP3381 Peptide, WBMT Peptide, 1110003N24Rik Peptide, Williams-Beuren syndrome chromosome region 22 Peptide, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog Peptide, BUD23, rRNA methyltransferase and ribosome maturation factor Peptide, williams Beuren syndrome chromosome region 22 Peptide, hypothetical protein Peptide, WBSCR22 Peptide, bud23.L Peptide, bud23 Peptide, CpipJ_CPIJ001394 Peptide, PAAG_00857 Peptide, MCYG_07273 Peptide, PGTG_07527 Peptide, PGTG_12505 Peptide, BUD23 Peptide, Bud23 Peptide
    Sujet
    This gene encodes a protein containing a nuclear localization signal and an S-adenosyl-L-methionine binding motif typical of methyltransferases, suggesting that the encoded protein may act on DNA methylation. This gene is deleted in Williams syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at 7q11.23. Alternatively spliced transcript variants have been found.

    Alias Symbols: HASJ4442, HUSSY-3, MGC19709, MGC2022, MGC5140, PP3381, WBMT

    Protein Size: 298
    Poids moléculaire
    32 kDa
    ID gène
    114049
    NCBI Accession
    NM_001202560, NP_001189489
    UniProt
    C9K060
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