STING/TMEM173 anticorps (AA 190-290)

N° du produit ABIN7871642

Cet anticorps Souris Monoclonal détecte spécifiquement STING/TMEM173 dans WB et IHC (p). Il présente une réactivité avec des échantillons de Humain.

Aperçu rapide pour STING/TMEM173 anticorps (AA 190-290) (ABIN7871642)

Antigène: STING/TMEM173 (TMEM173) (Transmembrane Protein 173 (TMEM173))

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp STING/TMEM173 est non-conjugé

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Classe de qualité: Carrier-free

Clone: STING1-7436

Détail du produit anti-STING/TMEM173 anticorps

Épitope: AA 190-290

Fonction: STING Antibody / Stimulator of interferon genes protein / ERIS / MITA (azide and preservative free)

Purification: Protein A/G affinity

Immunogène: A recombinant partial protein sequence (within amino acids 190-290) from the human protein was used as the immunogen for the STING antibody.

Isotype: IgG1, kappa

Information d'application

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

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: 1 mg/mL in 1X PBS, BSA free, sodium azide free

Agent conservateur: Azide free

Stock: -20 °C

Stockage commentaire: Aliquot the STING antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.

Détails sur STING/TMEM173

Antigène: STING/TMEM173 (TMEM173) (Transmembrane Protein 173 (TMEM173))

Autre désignation: STING

Sujet: TMEM173 (transmembrane protein 173), also called STING, ERIS and MITA, is a 379 amino acid protein encoded by a gene mapping to human chromosome 5. With 181 million base pairs encoding around 1,000 genes, chromosome 5 is about 6 % of human genomic DNA. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

UniProt: Q86WV6

Pathways: Activation of Innate immune Response