WRB Antikörper (AA 30-100)

Produktnummer ABIN6150261

Produktdetails anti-WRB Antikörper

Target: WRB (Tryptophan Rich Basic Protein (WRB))

Bindungsspezifität: AA 30-100

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser WRB Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), Immunohistochemistry (IHC)

Sequenz: SFSSFMSRVL QKDAEQESQM RAEIQDMKQE LSTVNMMDEF ARYARLERKI NKMTDKLKTH VKARTAQLAK I

Kreuzreaktivität: Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 30-100 of human WRB (NP_004618.2).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000,IHC,1:50 - 1:200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu WRB

Target: WRB (Tryptophan Rich Basic Protein (WRB))

Andere Bezeichnung: WRB (WRB Produkte)

Synonyme: pwi antikoerper, wu:ft06h05 antikoerper, zgc:101856 antikoerper, chd5 antikoerper, MGC89989 antikoerper, WRB antikoerper, UCP-1 antikoerper, DKFZp469L094 antikoerper, wrb antikoerper, mCHD5 antikoerper, MGC115192 antikoerper, CHD5 antikoerper, 5530402J05Rik antikoerper, C030018G21Rik antikoerper, Chd5 antikoerper, tryptophan rich basic protein antikoerper, tryptophan rich basic protein L homeolog antikoerper, WRB antikoerper, wrb antikoerper, wrb.L antikoerper, Wrb antikoerper

Hintergrund: This gene encodes a basic nuclear protein of unknown function. The gene is widely expressed in adult and fetal tissues. Since the region proposed to contain the gene(s) for congenital heart disease (CHD) in Down syndrome (DS) patients has been restricted to 21q22.2-22.3, this gene, which maps to 21q22.3, has a potential role in the pathogenesis of Down syndrome congenital heart disease. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.,WRB,CHD5,GET1,Neuroscience,Neurodegenerative Diseases,WRB

Molekulargewicht: 16 kDa/19 kDa

Gen-ID: 7485

UniProt: O00258