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WBSCR22 anticorps (C-Term)

WBSCR22 Reactivité: Humain WB Hôte: Lapin Polyclonal RB42713 unconjugated
N° du produit ABIN1881998
  • Antigène Voir toutes WBSCR22 Anticorps
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Épitope
    • 13
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 253-281, C-Term
    Reactivité
    • 35
    • 10
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Humain
    Hôte
    • 31
    • 4
    Lapin
    Clonalité
    • 33
    • 2
    Polyclonal
    Conjugué
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Cet anticorp WBSCR22 est non-conjugé
    Application
    • 27
    • 14
    • 8
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Homologie
    B, M
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogène
    This WBSCR22 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 253-281 amino acids from the C-terminal region of human WBSCR22.
    Clone
    RB42713
    Isotype
    Ig Fraction
    Top Product
    Discover our top product WBSCR22 Anticorps primaire
  • Indications d'application
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Agent conservateur
    Sodium azide
    Précaution d'utilisation
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Stock
    4 °C,-20 °C
    Date de péremption
    6 months
  • Lamesch, Li, Milstein, Fan, Hao, Szabo, Hu, Venkatesan, Bethel, Martin, Rogers, Lawlor, McLaren, Dricot, Borick, Cusick, Vandenhaute, Dunham, Hill, Vidal: "hORFeome v3.1: a resource of human open reading frames representing over 10,000 human genes." dans: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).

    Andersen, Lam, Leung, Ong, Lyon, Lamond, Mann: "Nucleolar proteome dynamics." dans: Nature, Vol. 433, Issue 7021, pp. 77-83, (2005) (PubMed).

    Merla, Ucla, Guipponi, Reymond: "Identification of additional transcripts in the Williams-Beuren syndrome critical region." dans: Human genetics, Vol. 110, Issue 5, pp. 429-38, (2002) (PubMed).

    Stanchi, Bertocco, Toppo, Dioguardi, Simionati, Cannata, Zimbello, Lanfranchi, Valle: "Characterization of 16 novel human genes showing high similarity to yeast sequences." dans: Yeast (Chichester, England), Vol. 18, Issue 1, pp. 69-80, (2001) (PubMed).

  • Antigène
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Autre désignation
    WBSCR22 (WBSCR22 Produits)
    Synonymes
    anticorps MGC82375, anticorps wbmt, anticorps pp3381, anticorps hussy-3, anticorps hasj4442, anticorps zgc:162306, anticorps HASJ4442, anticorps HUSSY-3, anticorps MERM1, anticorps PP3381, anticorps WBMT, anticorps 1110003N24Rik, anticorps Williams-Beuren syndrome chromosome region 22, anticorps BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog, anticorps BUD23, rRNA methyltransferase and ribosome maturation factor, anticorps williams Beuren syndrome chromosome region 22, anticorps hypothetical protein, anticorps WBSCR22, anticorps bud23.L, anticorps bud23, anticorps CpipJ_CPIJ001394, anticorps PAAG_00857, anticorps MCYG_07273, anticorps PGTG_07527, anticorps PGTG_12505, anticorps BUD23, anticorps Bud23
    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.
    Poids moléculaire
    31880
    NCBI Accession
    NP_001189489, NP_059998
    UniProt
    O43709
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