IL-24

IL-24 Molekülinformation

Englischer Name	Interleukin 24	Anzahl der inverkehr gebrachten Arzneimittel	0
Anzahl der klinischen Arzneimittel	1	Target-Alias	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
Höchste Forschungs- und Entwicklungsphase	Phase 1 Clinical

Englischer Name	Interleukin 24
Target-Alias	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
Anzahl der inverkehr gebrachten Arzneimittel	0
Anzahl der klinischen Arzneimittel	1
Höchste Forschungs- und Entwicklungsphase	Phase 1 Clinical

IL-24 Produktliste

Attribut
Protein (1)
Produktbibliothek
Online (1)
Spezies
Human (1)
Etikett
His Tag (1)
Marker
Unconjugated (1)

Produktnummer	Spezies	Expressionssystem	Produktbeschreibung	Proteinstruktur	Reinheit	Eigenschaften	Vorbestellen/Bestellen
IL4-H52H4	Human	HEK293	Human IL-24 Protein, His Tag (BLI verified)				In den Warenkorb legen

Gesamtmenge1

IL-24 Molekülhintergrund

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.