2010
DOI: 10.1016/j.jchromb.2010.09.009
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An automated packed Protein G micro-pipette tip assay for rapid quantification of polyclonal antibodies in ovine serum

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Cited by 18 publications
(9 citation statements)
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“…Chromatographic separations are often used as analytical tools for the detection and measurement of analytes of interest in process streams (Table S5). For example, Protein A analytical scale columns (Hober et al, 2007) or micro‐pipette assays (Chhatre et al, 2010) measure the total content of mAb in a sample. For the latter method, the main contribution to the total analytical time stems from the liquid handling of samples.…”
Section: Resultsmentioning
confidence: 99%
“…Chromatographic separations are often used as analytical tools for the detection and measurement of analytes of interest in process streams (Table S5). For example, Protein A analytical scale columns (Hober et al, 2007) or micro‐pipette assays (Chhatre et al, 2010) measure the total content of mAb in a sample. For the latter method, the main contribution to the total analytical time stems from the liquid handling of samples.…”
Section: Resultsmentioning
confidence: 99%
“…Feed: Stocks of ovine serum containing polyclonal antibody must be maintained at −20 °C for long-term storage. To avoid the potentially deleterious impact of repeated freeze-thaw cycles of bulk material [7], it is recommended that small aliquots of around 1.5-2.0 mL volumes are frozen. Samples should be thawed fully to ambient temperature prior to experimentation.…”
Section: Materials and Equipmentmentioning
confidence: 99%
“…To create an isotherm curve requires one to know the number of cycles needed to achieve equilibrium between solid and liquid phase at each concentration; hence isotherm data can be obtained from the end point of uptake curve data by material balance (see below) (see Notes 9-12). Uptake curves as a function of time can be plotted either in terms of the residual feed concentration, i.e., C = f(t), or in a normalized form by dividing individual data points by the initial feed antibody concentration, i.e., C/C 0 = f(t) [7]. The value of time at each data point accounts for the accumulated period covering both the aspirate and dispense steps.…”
Section: Liquid Handlingmentioning
confidence: 99%
“…A large number of researches focus on the high throughput screening (HTS) which is an essential part of drug discovery and development (Gribbon & Andreas 2005;Mishra et al 2008). Many studies have contributed to microbial fermentation (Kostov et al 2001;Rios-Solis et al 2013 (Saitoh & Yoshimori 2008), precipitation (Knevelman et al 2010;Titchener-Hooker et al 2008) and chromatography (Chhatre et al 2010;Wiendahl et al 2008). …”
Section: Application Of High Throughput Techniques In Bioprocess Devementioning
confidence: 99%
“…The tips enable the liquid handling system to investigate the whole chromatography processes. Several studies used micropipette chromatography tips to model the performance of column (Coffman et al 2008;Chhatre et al 2010). The third approach is to apply miniature columns.…”
Section: Chromatographymentioning
confidence: 99%