IL-24

IL-24 Informations sur la molécule

Nom anglais	Interleukin 24	Nombre de médicaments commercialisés	0
Nombre de médicaments cliniques	1	Alias de la cible	ST16，Interleukin-24，IL24，MDA-7，Suppression of tumorigenicity 16 protein，IL-24，Interleukin 24，Suppression Of Tumorigenicity 16 (Melanoma Differentiation)，Melanoma Differentiation-Associated Gene 7 Protein，IL-4-Induced Secreted Protein，MDA7，Melanoma Differentiation Association Protein 7，Melanocyte-Associated Mda-7，IL10B，C49A，FISP，MOB5，Mob-5
Phase de R&D la plus avancée	Phase 1 Clinical

Nom anglais	Interleukin 24
Alias de la cible	ST16，Interleukin-24，IL24，MDA-7，Suppression of tumorigenicity 16 protein，IL-24，Interleukin 24，Suppression Of Tumorigenicity 16 (Melanoma Differentiation)，Melanoma Differentiation-Associated Gene 7 Protein，IL-4-Induced Secreted Protein，MDA7，Melanoma Differentiation Association Protein 7，Melanocyte-Associated Mda-7，IL10B，C49A，FISP，MOB5，Mob-5
Nombre de médicaments commercialisés	0
Nombre de médicaments cliniques	1
Phase de R&D la plus avancée	Phase 1 Clinical

IL-24 Liste de produits

Attribut
Protein (1)
Bibliothèque de produits
En ligne (1)
Espèces
Human (1)
Étiquette
His Tag (1)
Marqueur
Unconjugated (1)

Numéro de produit	Espèces	Système d'expression	Description du produit	Structure protéique	Pureté	Caractéristiques	Pré-commande/Commande
IL4-H52H4	Human	HEK293	Human IL-24 Protein, His Tag (BLI verified)				Ajouter au panier

Quantité totale1

IL-24Contexte de la molécule

Interleukin-24 (IL-24, also known as melanoma differentiation-associated gene-7) belongs to the family of IL-10-related cytokines, which includes IL-10, -19, -20, -22, -24 and -26. Interleukin 24 signals through two heterodimeric receptors: IL-20R1/IL-20R2 and IL-22R1/IL-20R2. Upon binding to its receptors, IL-24 induces rapid activation of Stat-1 and Stat-3 transcription factors, which appear to play a role in cell survival and proliferation . Structurally and functionally, IL-24 is highly conserved across species.IL-24 has been shown to possess cancer-specific apoptosis-inducing activity, and has therefore been suggested as a potential anti-cancer agent.