Ganitumab
CAS No. 905703-97-1
Ganitumab( —— )
Catalog No. M36729 CAS No. 905703-97-1
Ganitumab (AMG 479) is a highly potent monoclonal antibody targeting the type 1 insulin-like growth factor receptor (IGF1R). Recognized for binding IGF1R at low concentrations with a KD value of 0.22 nM, Ganitumab inhibits IGF1R interactions with IGF1 and IGF2 in mice, making it useful for cancer research.
Purity : >98% (HPLC)
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Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 2MG | 439 | Get Quote |
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| 5MG | 717 | Get Quote |
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| 10MG | 1121 | Get Quote |
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| 25MG | 1638 | Get Quote |
|
| 50MG | 2199 | Get Quote |
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| 500MG | Get Quote | Get Quote |
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| 1G | Get Quote | Get Quote |
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Biological Information
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Product NameGanitumab
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NoteResearch use only, not for human use.
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Brief DescriptionGanitumab (AMG 479) is a highly potent monoclonal antibody targeting the type 1 insulin-like growth factor receptor (IGF1R). Recognized for binding IGF1R at low concentrations with a KD value of 0.22 nM, Ganitumab inhibits IGF1R interactions with IGF1 and IGF2 in mice, making it useful for cancer research.
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DescriptionGanitumab (AMG 479) is a recombinant human monoclonal antibody to the human type 1 insulin-like growth factor receptor (IGF1R). Ganitumab recognizes murine IGF1R with sub-nanomolar affinity (KD=0.22 nM) and inhibits the interaction of murine IGF1R with IGF1 and IGF2. Ganitumab can be used in research of cancer.
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In VitroWestern Blot Analysis Cell Line:CT26 cells Concentration:0.032-500 nM Incubation Time:10 minutes Result:Inhibited IGF1-induced autophosphorylation of mIGF1R in CT26 murine colon carcinoma cells in a dose-dependent manner.
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In VivoAnimal Model:Na?ve and tumor-bearing miceDosage:1 mg/doseAdministration:Intraperitoneal injectionResult:Inhibited the IGF1-induced activation of mIGF1R and inhibited 80% tumor growth.Animal Model:Male athymic nude mice Dosage:300 μg/dose Administration:Intraperitoneal injection, twice per week for a total of five doses Result:Had significantly higher serum glucose levels than hIgG1-pretreated mice.Increased serum levels of mIGF1, mIGFPB3 and mGH.Animal Model:Female athymic nude mice Dosage:300 μg/dose Administration:Intraperitoneal injection, twice per week for a total of five dosesResult:Reduced the number of peripheral neutrophils up to 50% compared with hIgG1 controls.
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Synonyms——
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PathwayAngiogenesis
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TargetIGF-1R
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RecptorIGF-1R
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Research Area——
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Indication——
Chemical Information
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CAS Number905703-97-1
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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
1. Moody G, et, al. IGF1R blockade with ganitumab results in systemic effects on the GH-IGF axis in mice. J Endocrinol. 2014 Mar 17;221(1):145-55.?
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