NSMCE2 anticorps (AA 14-228)

N° du produit ABIN7870621

Cet anticorps anti-NSMCE2 Polyclonal Lapin (ABIN7870621) détecte spécifiquement NSMCE2 dans WB, ELISA, IF, FACS et IP. L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour NSMCE2 anticorps (AA 14-228) (ABIN7870621)

Antigène: NSMCE2 (E3 SUMO-Protein Ligase NSE2 (NSMCE2))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp NSMCE2 est non-conjugé

Application: Western Blotting (WB), ELISA, Immunofluorescence (IF), Flow Cytometry (FACS), Immunoprecipitation (IP)

Détail du produit anti-NSMCE2 anticorps

Épitope: AA 14-228

Fonction: NSMCE2 Antibody / NSE2 / MMS21

Purification: Antigen affinity purified

Immunogène: An E.coli-derived human recombinant protein (F14-D228) was used as the immunogen for the NSMCE2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the NSMCE2 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 NSMCE2 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 NSMCE2

Antigène: NSMCE2 (E3 SUMO-Protein Ligase NSE2 (NSMCE2))

Autre désignation: NSMCE2

Sujet: This gene encodes a member of a family of E3 small ubiquitin-related modifier (SUMO) ligases that mediates the attachment of a SUMO protein to proteins involved in nuclear transport, transcription, chromosome segregation and DNA repair. The encoded protein is part of the structural maintenance of chromosomes (SMC) 5/6 complex which plays a key role genome maintenance, facilitating chromosome segregation and suppressing mitotic recombination. A knockout of the orthologous mouse gene is lethal prior to embryonic day 10.5. Naturally occurring mutations in this gene, that abolish the SUMO ligase activity, are associated with primordial dwarfism and extreme insulin resistance.

UniProt: Q96MF7