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US Patent 11850535 Methods for quantitating individual antibodies from a mixture

Patent 11850535 was granted and assigned to Regeneron Pharmaceuticals on December, 2023 by the United States Patent and Trademark Office.

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Contents

Is a
Patent
Patent
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Patent attributes

Patent Applicant
Regeneron Pharmaceuticals
Regeneron Pharmaceuticals
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Current Assignee
Regeneron Pharmaceuticals
Regeneron Pharmaceuticals
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Patent Jurisdiction
United States Patent and Trademark Office
United States Patent and Trademark Office
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Patent Number
118505350
Patent Inventor Names
Long Xu0
Dingjiang Liu0
Lin Luo0
Date of Patent
December 26, 2023
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Patent Application Number
180678030
Date Filed
December 19, 2022
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Patent Citations
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US Patent 7303747 Use of VEGF inhibitors for treatment of eye disorders
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US Patent 7306799 Use of VEGF inhibitors for treatment of eye disorders
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US Patent RE40070 Antibody purification
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US Patent 7374757 Modified chimeric polypeptides with improved pharmacokinetic properties
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US Patent 7374758 Modified chimeric polypeptides with improved pharmacokinetic properties and methods of using thereof
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US Patent 7385040 Antibody purification
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US Patent 7393631 Method for purifying adenoviruses
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US Patent 7427659 Process for purifying proteins in a hydrophobic interaction chromatography flow-through fraction
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Patent Primary Examiner
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Jennifer Wecker
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CPC Code
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C07K 16/065
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C07K 16/10
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G01N 30/02
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G01N 33/6854
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G01N 2030/027
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G01N 30/88
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G01N 2030/8831
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A61P 11/00
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Patent abstract

The present disclosure relates to, inter alia, a method of quantitating an amount of an antibody molecule from a mixture comprising two or more antibody molecules, comprising separating each of the two or more antibody molecules from the mixture by hydrophobic interaction chromatography high performance liquid chromatography (HIC-HPLC) and quantitating an amount of each antibody molecule, wherein the molecular weight of each antibody molecule is within 15 kDa of any other antibody molecule in the mixture and either each antibody molecule is different from another antibody molecule in the mixture by more than about 0.25 unit on the Kyte & Doolittle hydropathy scale or each of the antibody molecules when nm alone on HIC-HPLC elutes at distinct run time with little overlap from the other antibody molecules in the mixture, or both.

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