Golimumab

CAS No. 476181-74-5

Golimumab( —— )

Catalog No. M36680 CAS No. 476181-74-5

Golimumab (CNTO-148) is a potent humanized anti-TNFα IgG1κ monoclonal antibody with anti-inflammatory and anticancer activity.

Purity : >98% (HPLC)

COA Datasheet HNMR HPLC MSDS Handing Instructions
Size Price / USD Stock Quantity
2MG 369 Get Quote
5MG 534 Get Quote
10MG 744 Get Quote
25MG 1095 Get Quote
50MG 1463 Get Quote
500MG Get Quote Get Quote
1G Get Quote Get Quote

Biological Information

  • Product Name
    Golimumab
  • Note
    Research use only, not for human use.
  • Brief Description
    Golimumab (CNTO-148) is a potent humanized anti-TNFα IgG1κ monoclonal antibody with anti-inflammatory and anticancer activity.
  • Description
    Golimumab (CNTO-148) is a potent human IgG1 TNFα antagonist monoclonal antibody. Golimumab has anti-inflammation activitity and inhibits IL-6 and IL-1β production. Golimumab acts via targeting and neutralizing TNF to prevent inflammation and destruction of cartilage and bone. Golimumab has the anticancer activity and induces cell apoptosis. Golimumab can be used for rheumatoid arthritis, Crohn's disease and cancer research.
  • In Vitro
    Golimumab (CNTO-148) (0.1-10 μg /mL; 24-72 hours; transmembrane TNFα–transfected Jurkat cells) induces reductions in the viability of transmembrane TNFα–expressing cells.Golimumab (CNTO-148) (10 μg /mL; 48 hours; transmembrane TNFα–transfected Jurkat cells) induces apoptosis, increase the levels of active caspase-3 and induces apoptotic DNA fragmentation.Cell Viability Assay Cell Line:Transmembrane TNFα–transfected Jurkat cells Concentration:0.1, 1 and 10 μg/mL Incubation Time:24, 48 and 72 hours Result:Reduced cell viability in a dose- and time-dependent manner.Apoptosis Analysis Cell Line:Transmembrane TNFα–transfected Jurkat cells Concentration:10 μg /mL Incubation Time:48 hours Result:Had the percentage of apoptotic cells for 30.29%.Western Blot Analysis Cell Line:Transmembrane TNFα–transfected Jurkat cellsConcentration:10 μg /mL Incubation Time:48 hours Result:Increased the levels of active caspase-3 and induces apoptotic DNA fragmentation.
  • In Vivo
    Golimumab (CNTO-148) (24 mg/kg; i.h.; daily, for 7 days; swiss-albino healthy male mice) inhibits oxidative stress, apoptotic cell death inflammatory response, thus improving renal function. Golimumab reduces all markers of kidney injury and attenuates cell death.Golimumab (CNTO-148) (1-10 mg/kg; i.p.;daily; for 4 weeks; Tg197 transgenic mouse model) relieves TNFα-induced arthritis in a mouse model of human.Animal Model:Swiss-albino healthy male mice Dosage:24 mg/kg Administration: Subcutaneous injection; daily, for 7 days Result:Reduced serum parameters like BUN, NGAL creatinine, cystatin C, and urinary parameters like KIM-1, NAG, albumin clusterin.Animal Model:Swiss-albino healthy male miceDosage:24 mg/kg Administration:Subcutaneous injection; daily, for 7 days Result:Inhibited oxidative stress, reduces MDA concentrations and increases the GSH and catalase levels.Animal Model:Swiss-albino healthy male mice Dosage:24 mg/kg Administration: Subcutaneous injection; daily, for 7 days Result:Inhibitd cisplatin-induced inflammation, decreased TNF-α, including IL-6, IL-1β, MCP-1, ICAM-1, and TGF-β1 levels and increases IL-10 concentrations, reduced caspase 3 in cisplatin injected mice kidneys.Animal Model:Tg197 transgenic mouse model Dosage:1 and 10 mg/kg Administration:Intraperitoneal injection;for 4 weeks Result:Reduced the arthritic index.
  • Synonyms
    ——
  • Pathway
    Apoptosis
  • Target
    TNF
  • Recptor
    TNF
  • Research Area
    ——
  • Indication
    ——

Chemical Information

  • CAS Number
    476181-74-5
  • Formula Weight
    146.93KD
  • Molecular Formula
    ——
  • Purity
    >98% (HPLC)
  • Solubility
    ——
  • SMILES
    ——
  • Chemical Name
    ——

Shipping & Storage Information

  • Storage
    (-20℃)
  • Shipping
    With Ice Pack
  • Stability
    ≥ 2 years

Reference

1. Ueda N, et, al. The cytotoxic effects of certolizumab pegol and golimumab mediated by transmembrane tumor necrosis factor α. Inflamm Bowel Dis. 2013 May;19(6):1224-31.?
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