ISCU anticorps (AA 1-167)

N° du produit ABIN6142546

Cet anticorps anti-ISCU Polyclonal Lapin (ABIN6142546) détecte spécifiquement ISCU dans WB. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour ISCU anticorps (AA 1-167) (ABIN6142546)

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ISCU est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-ISCU anticorps

Épitope: AA 1-167

Séquence: MAAAGAFRLR RAASALLLRS PRLPARELSA PARLYHKKVV DHYENPRNVG SLDKTSKNVG TGLVGAPACG DVMKLQIQVD EKGKIVDARF KTFGCGSAIA SSSLATEWVK GKTVEEALTI KNTDIAKELC LPPVKLHCSM LAEDAIKAAL ADYKLKQEPK KGEAEKK

Réactivité croisée: Humain

Attributs du produit: Polyclonal Antibodies

Immunogène: Recombinant fusion protein containing a sequence corresponding to amino acids 1-167 of human ISCU (NP_998760.1).

Isotype: IgG

Information d'application

Indications d'application: WB,1:500 - 1:2000

Commentaires:

HIGH QUALITY

Restrictions: For Research Use only

Stockage

Format: Liquid

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

Agent conservateur: Sodium azide

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

Stock: -20 °C

Stockage commentaire: Store at -20°C. Avoid freeze / thaw cycles.

Détails sur ISCU

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

Autre désignation: ISCU

Sujet: 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.,ISCU,2310020H20Rik,HML,ISU2,NIFU,NIFUN,hnifU,Signal Transduction,Endocrine & Metabolism,ISCU

Poids moléculaire: 15 kDa/17 kDa

ID gène: 23479

UniProt: Q9H1K1