ISCU anticorps

N° du produit ABIN7261091

Détail du produit anti-ISCU anticorps

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ISCU est non-conjugé

Application: Western Blotting (WB)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: A synthetic Peptide of human ISCU

Isotype: IgG

Information d'application

Indications d'application: WB 1:500-1:1000

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

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 (ISCU Produits)

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

Poids moléculaire:

Observed_MW: 26 kDa

Calculated_MW: 15 kDa/17 kDa

ID gène: 23479

UniProt: Q9H1K1