MOCS1 anticorps (AA 52-584)

N° du produit ABIN7875568

Cet anticorps anti-MOCS1 Polyclonal Lapin (ABIN7875568) détecte spécifiquement MOCS1 dans WB, ELISA et IF. L’anticorps est réactif avec des échantillons de Humain, Souris et Rat.

Aperçu rapide pour MOCS1 anticorps (AA 52-584) (ABIN7875568)

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, Immunofluorescence (IF)

Détail du produit anti-MOCS1 anticorps

Épitope: AA 52-584

Fonction: MOCS1 Antibody

Purification: Antigen affinity chromatography

Immunogène: An E.coli-derived human recombinant protein (amino acids E52-R584) 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