ISCU Antikörper

Produktnummer ABIN7246487

Produktdetails anti-ISCU Antikörper

Target: ISCU (Iron-sulfur cluster assembly enzyme ISCU, mitochondrial (ISCU))

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser ISCU Antikörper ist unkonjugiert

Applikation: Western Blotting (WB), ELISA

Produktmerkmale: Polyclonal Antibody

Aufreinigung: Antigen affinity purification

Immunogen: Fusion protein of human ISCU

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB 1:500-1:2000, ELISA 1:5000-1:10000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 0.96 mg/mL

Buffer: PBS with 0.05 % Sodium azide and 40 % Glycerol, pH 7.4

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 ISCU

Target: ISCU (Iron-sulfur cluster assembly enzyme ISCU, mitochondrial (ISCU))

Andere Bezeichnung: ISCU (ISCU Produkte)

Synonyme: nifun antikoerper, zC191D15.3 antikoerper, si:ch211-191d15.3 antikoerper, 2310020H20Rik antikoerper, HML antikoerper, ISU2 antikoerper, NIFU antikoerper, NIFUN antikoerper, hnifU antikoerper, RGD1309562 antikoerper, AA407971 antikoerper, Nifu antikoerper, Nifun antikoerper, iron-sulfur cluster assembly enzyme ISCU, mitochondrial antikoerper, iron-sulfur cluster assembly enzyme antikoerper, iron-sulfur cluster assembly enzyme a antikoerper, LOC409130 antikoerper, ISCU antikoerper, iscua antikoerper, Iscu antikoerper

Hintergrund: This gene encodes a component of the iron-sulfur (Fe-S) cluster scaffold. Fe-S clusters are cofactors that play a role in the function of a diverse set of enzymes, including those that regulate metabolism, iron homeostasis, and oxidative stress response. Alternative splicing results in transcript variants encoding different protein isoforms that localize either to the cytosol or to the mitochondrion. Mutations in this gene have been found in patients with hereditary myopathy with lactic acidosis. A disease-associated mutation in an intron may activate a cryptic splice site, resulting in the production of a splice variant encoding a putatively non-functional protein. A pseudogene of this gene is present on chromosome 1.

Molekulargewicht:

Observed_MW: Refer to figures

Calculated_MW: 18 kDa

UniProt: Q9H1K1