STING/TMEM173 anticorps (AA 190-290)

N° du produit ABIN7871641

Cet anticorps anti-STING/TMEM173 Monoclonal Souris (Clone STING1-7434) (ABIN7871641) détecte spécifiquement STING/TMEM173 dans IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour STING/TMEM173 anticorps (AA 190-290) (ABIN7871641)

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

Reactivité: Humain

Hôte: Souris

Clonalité: Monoclonal

Conjugué: Cet anticorp STING/TMEM173 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Clone: STING1-7434

Détail du produit anti-STING/TMEM173 anticorps

Épitope: AA 190-290

Fonction: Stimulator of interferon genes protein Antibody / STING1 / TMEM17 / ERIS / MITA

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 Stimulator of interferon genes protein antibody.

Isotype: IgG, kappa

Information d'application

Indications d'application: Optimal dilution of the Stimulator of interferon genes protein antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 0.2 mg/mL

Buffer: 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide

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: Aliquot the Stimulator of interferon genes protein 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: Stimulator of interferon genes protein

Sujet: TMEM173 (transmembrane protein 173), also called STING (Stimulator of interferon genes protein), 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