MOCS1 anticorps (AA 52-84)

N° du produit ABIN7875572

Cet anticorps Lapin Polyclonal détecte spécifiquement MOCS1 dans WB, ELISA, IHC (p), IF et FACS. Il présente une réactivité avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour MOCS1 anticorps (AA 52-84) (ABIN7875572)

Antigène: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp MOCS1 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (IF), Flow Cytometry (FACS)

Détail du produit anti-MOCS1 anticorps

Épitope: AA 52-84

Fonction: MOCS1 Antibody / Molybdenum cofactor biosynthesis protein 1

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (E52-R84) was used as the immunogen for the MOCS1 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the MOCS1 antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the MOCS1 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur MOCS1

Antigène: MOCS1 (Molybdenum Cofactor Synthesis 1 (MOCS1))

Autre désignation: MOCS1

Sujet: Molybdenum cofactor biosynthesis protein 1 is a protein that in humans and other animals, fungi, and cellular slime molds, is encoded by the MOCS1 gene. Molybdenum cofactor biosynthesis is a conserved pathway leading to the biological activation of molybdenum. The protein encoded by this gene is involved in this pathway. This gene was originally thought to produce a bicistronic mRNA with the potential to produce two proteins (MOCS1A and MOCS1B) from adjacent open reading frames. However, only the first open reading frame (MOCS1A) has been found to encode a protein from the putative bicistronic mRNA, whereas additional splice variants are likely to produce a fusion between the two open reading frames. This gene is defective in patients with molybdenum cofactor deficiency, type A. A related pseudogene has been identified on chromosome 16.

UniProt: Q9NZB8