Methods for high-throughput screening of cell lines
A cell line, high-throughput technology, applied in the field of screening cell lines, can solve the problems of inability to produce post-translational modifications, waste of time and resources, and protein structure abnormalities
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Embodiment 1
[0112] High-throughput screening of human Fc protein assays
[0113] 1. Preparation of anti-Aβ standard
[0114] Standard curve buffer was prepared in 16 assay plates (Corning / Costar, Corning, NY) by mixing 20 ul of medium R5CD1 and 24 ml of assay buffer (PBS w / 0.05% Tween 20 and 1% bovine serum albumin) (SCB). A 0.3 mg / ml intermediate standard was prepared using 6 ul 32.5 mg / ml reference standard and 644 ul SCB (prepared fresh each time). A lug / ml standard was placed in a well called A1 and an additional well called H1 of a 2ml deep well plate. In 16 assay plates, well A1 contained 6ul of 0.3 mg / ml intermediate standard and 1794ul of SCB. Repeat the process for hole H1. For each of the 16 assay plates, serial dilutions were prepared by taking 900ul of the solution in the wells and adding 900ul of SCB. Dilutions were dispensed at 50ul per standard well.
[0115] 2. Preparation of controls
[0116] Controls were prepared to create an intermediate control at a conce...
Embodiment 2
[0138] High-throughput purification and identification of suitable cell culture conditions
[0139] 1. Manual protein purification using centrifugation
[0140] The high-throughput titration screening method of Example 1 can be combined with the high-throughput purification method detailed below to facilitate potential improvements in cell culture.
[0141] Thin layer resin in 20% ethanol. Additional 20% ethanol solution was added to make up 50% of the final volume. The solution was mixed well and dispensed in 200uL aliquots per well of filter plates (Whatman 7700-2804, longdrip, 25um, 96 well x 800uL, Whatman LabSciences, Orange, NJ). Filter plates were stacked on top of empty microplates (Corning / Costar, Corning, NY) and centrifuged (Sorvall Legend RT) at 700 rpm (approximately equal to 104G) for 3 minutes to remove 20% ethanol. Then, 200 uL per well of RODI water was added and the plates were centrifuged for 3 minutes with an empty microtiter plate underneath. Repea...
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