WBSCR22 Antikörper (C-Term)

Produktnummer ABIN1881998

Produktdetails anti-WBSCR22 Antikörper

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Bindungsspezifität: AA 253-281, C-Term

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WBSCR22 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

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.

Klon: RB42713

Isotyp: Ig Fraction

Anwendungsinformationen

Applikationshinweise: WB: 1:1000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

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

Referenzen für anti-WBSCR22 Antikörper (ABIN1881998)

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).

Details zu WBSCR22

Target: WBSCR22 (Williams Beuren Syndrome Chromosome Region 22 (WBSCR22))

Andere Bezeichnung: WBSCR22 (WBSCR22 Produkte)

Synonyme: MGC82375 antikoerper, wbmt antikoerper, pp3381 antikoerper, hussy-3 antikoerper, hasj4442 antikoerper, zgc:162306 antikoerper, HASJ4442 antikoerper, HUSSY-3 antikoerper, MERM1 antikoerper, PP3381 antikoerper, WBMT antikoerper, 1110003N24Rik antikoerper, Williams-Beuren syndrome chromosome region 22 antikoerper, BUD23, rRNA methyltransferase and ribosome maturation factor L homeolog antikoerper, BUD23, rRNA methyltransferase and ribosome maturation factor antikoerper, williams Beuren syndrome chromosome region 22 antikoerper, hypothetical protein antikoerper, WBSCR22 antikoerper, bud23.L antikoerper, bud23 antikoerper, CpipJ_CPIJ001394 antikoerper, PAAG_00857 antikoerper, MCYG_07273 antikoerper, PGTG_07527 antikoerper, PGTG_12505 antikoerper, BUD23 antikoerper, Bud23 antikoerper

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