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WBSCR22 Antikörper (C-Term)

Der Kaninchen Polyklonal Anti-WBSCR22-Antikörper wurde für WB validiert. Er ist geeignet, WBSCR22 in Proben von Human zu detektieren. Es sind 4+ Publikationen verfügbar.
Produktnummer ABIN1881998

Kurzübersicht für WBSCR22 Antikörper (C-Term) (ABIN1881998)

Target

Alle WBSCR22 Antikörper anzeigen
WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Reaktivität

  • 29
  • 10
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Human

Wirt

  • 25
  • 4
Kaninchen

Klonalität

  • 27
  • 2
Polyklonal

Konjugat

  • 17
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
Dieser WBSCR22 Antikörper ist unkonjugiert

Applikation

  • 22
  • 9
  • 7
  • 5
  • 4
  • 2
  • 2
  • 1
  • 1
  • 1
Western Blotting (WB)

Klon

RB42713
  • Bindungsspezifität

    • 8
    • 3
    • 3
    • 2
    • 1
    • 1
    • 1
    • 1
    • 1
    AA 253-281, C-Term

    Homologie

    B, M

    Aufreinigung

    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.

    Isotyp

    Ig Fraction
  • Applikationshinweise

    WB: 1:1000

    Beschränkungen

    Nur für Forschungszwecke einsetzbar
  • Format

    Liquid

    Buffer

    Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

    Konservierungsmittel

    Sodium azide

    Vorsichtsmaßnahmen

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Lagerung

    4 °C,-20 °C

    Haltbarkeit

    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))

    Andere Bezeichnung

    WBSCR22

    Hintergrund

    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.

    Molekulargewicht

    31880

    NCBI Accession

    NP_001189489, NP_059998

    UniProt

    O43709
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