BZW2 Antikörper (FITC)

Produktnummer ABIN1400240

Produktdetails anti-BZW2 Antikörper (FITC)

Target: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Reaktivität: Human, Maus, Ratte

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser BZW2 Antikörper ist konjugiert mit FITC

Applikation: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Kreuzreaktivität: Human, Maus, Ratte

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human BZW2

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: IF(IHC-P) 1:50-200

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Konservierungsmittel: ProClin

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

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Haltbarkeit: 12 months

Details zu BZW2

Target: BZW2 (Basic Leucine Zipper and W2 Domains 2 (BZW2))

Andere Bezeichnung: BZW2 (BZW2 Produkte)

Synonyme: HSPC028 antikoerper, MGC84347 antikoerper, MST017 antikoerper, MSTP017 antikoerper, 1110001I24Rik antikoerper, Bdm2 antikoerper, Hfb2 antikoerper, zgc:55580 antikoerper, basic leucine zipper and W2 domains 2 antikoerper, basic leucine zipper and W2 domains 2 L homeolog antikoerper, BZW2 antikoerper, bzw2.L antikoerper, Bzw2 antikoerper, bzw2 antikoerper

Hintergrund:

Synonyms: HSPC028, MSTP017 antibody Basic leucine zipper and W2 domain containing protein 2, Basic leucine zipper and W2 domains 2, BZW 2, MST017, BZW2_HUMAN.

Background: BZW2, also known as HSPC028 or MSTP017, is a 419 amino acid protein that contains one W2 domain and is thought to be involved in neuronal differentiation. The gene encoding BZW2 maps to human chromosome 7. Chromosome 7 houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders, including cases of acute myelogenous leukemia and myelodysplasia.

Gen-ID: 28969

Pathways: SARS-CoV-2 Protein Interaktom