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WBSCR22 antibody (C-Term)

WBSCR22 Reactivity: Human WB Host: Rabbit Polyclonal RB42713 unconjugated
Catalog No. ABIN1881998
  • Target See all WBSCR22 Antibodies
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Binding Specificity
    • 13
    • 8
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 253-281, C-Term
    Reactivity
    • 35
    • 10
    • 5
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    Human
    Host
    • 31
    • 4
    Rabbit
    Clonality
    • 33
    • 2
    Polyclonal
    Conjugate
    • 18
    • 3
    • 2
    • 2
    • 2
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    • 1
    This WBSCR22 antibody is un-conjugated
    Application
    • 27
    • 14
    • 8
    • 5
    • 5
    • 2
    • 2
    • 1
    • 1
    • 1
    Western Blotting (WB)
    Predicted Reactivity
    B, M
    Purification
    This antibody is purified through a protein A column, followed by peptide affinity purification.
    Immunogen
    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 Primary Antibody
  • Application Notes
    WB: 1:1000
    Restrictions
    For Research Use only
  • Format
    Liquid
    Buffer
    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
    Preservative
    Sodium azide
    Precaution of Use
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    Storage
    4 °C,-20 °C
    Expiry Date
    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." in: Genomics, Vol. 89, Issue 3, pp. 307-15, (2007) (PubMed).

    Andersen, Lam, Leung, Ong, Lyon, Lamond, Mann: "Nucleolar proteome dynamics." in: 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." in: 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." in: Yeast (Chichester, England), Vol. 18, Issue 1, pp. 69-80, (2001) (PubMed).

  • Target
    WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))
    Alternative Name
    WBSCR22 (WBSCR22 Products)
    Synonyms
    MGC82375 antibody, wbmt antibody, pp3381 antibody, hussy-3 antibody, hasj4442 antibody, zgc:162306 antibody, HASJ4442 antibody, HUSSY-3 antibody, MERM1 antibody, PP3381 antibody, WBMT antibody, 1110003N24Rik antibody, Williams-Beuren syndrome chromosome region 22 antibody, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog antibody, BUD23, rRNA methyltransferase and ribosome maturation factor antibody, williams Beuren syndrome chromosome region 22 antibody, hypothetical protein antibody, WBSCR22 antibody, bud23.L antibody, bud23 antibody, CpipJ_CPIJ001394 antibody, PAAG_00857 antibody, MCYG_07273 antibody, PGTG_07527 antibody, PGTG_12505 antibody, BUD23 antibody, Bud23 antibody
    Background
    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.
    Molecular Weight
    31880
    NCBI Accession
    NP_001189489, NP_059998
    UniProt
    O43709
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