Oxelumab
CAS No. 1186098-83-8
Oxelumab( —— )
Catalog No. M36764 CAS No. 1186098-83-8
Oxelumab (R 4930) is a human monoclonal antibody targeting OX40L, and could be used to study asthma.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 429 | In Stock |
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| 10MG | 677 | In Stock |
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| 25MG | 1026 | In Stock |
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| 50MG | 1358 | In Stock |
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| 100MG | 1832 | In Stock |
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| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameOxelumab
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NoteResearch use only, not for human use.
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Brief DescriptionOxelumab (R 4930) is a human monoclonal antibody targeting OX40L, and could be used to study asthma.
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DescriptionOxelumab (R 4930) is a human monoclonal antibody against the OX40 ligand (OX40L). Oxelumab can be used for the research of asthma.
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In VitroCell Proliferation Assay Cell Line:Natural Killer (NK) cell lines Concentration:10 μg/mL Incubation Time:3 days Result:Inhibited cell proliferation of NK cells.
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In VivoAnimal Model:NSG mice with PBMCs from UC patients with simple clinical colitis activity index (SCCAI) Dosage:5 and 30 mg/kg Administration:Intraperitoneal injectionon; 5 and 30 mg/kg, once daily, on days 6 and 13 Result:Reversed the ethanol-induced colon dilated and the lost of distinct pattern of pellets. Decreased the level of IL-6 and increased the concentrations of glutamic acid. Reduced frequencies of splenic human effector memory T cells and switched B cells.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorInterleukin
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Research Area——
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Indication——
Chemical Information
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CAS Number1186098-83-8
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Formula Weight
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Molecular Formula——
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Purity>98% (HPLC)
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Solubility——
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SMILES——
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
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EPZ032597
EPZ032597 is a novel selective inhibitor of SMYD2 with an IC50 of 16 nM. EPZ032597 has anticancer activity and can be used to prevent and treat pancreatic cancer.
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N-Succinimidyl-S-ace...
N-Succinimidyl S-acetylthioacetate (SATA) is a protein modification agent that introduces thiol-groups into protein molecules and adds sulfhydryl groups in a protected form to proteins and other amine-containing molecules for later reaction with sulfhydryl reactive crosslinkers such as Sulfo-SMCC, Sulfo-MBS, etc.
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Sarmenoside II
Sarmenoside II is a flavonol glycoside with activity that inhibits lipid accumulation. Sarmenoside II inhibits albumin-oleate-induced lipid accumulation in HepG2 cells by approximately 30% at 100 μM.
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