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In total, 186 proteins were immunoreactive to at least one sera type and of these, 105 were immunoreactive to all sera screened.
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The most important factors in significantly affecting cell growth and differentiation were the sera types added to basal DMEM.
Moreover, we have tested the effects of sera types on proliferation, morphology, population doubling and viability of primary equine bronchial fibroblasts.
In concordance, sera types affect other various cell types in a similar way: bovine adipocytes and sheep skeletal muscle satellite cells proliferated rapidly, when FBS was supplemented to growth medium instead of HS; thus, FBS-containing medium is often used as growth medium in these cultures [ 31, 32].
Consistent with this, although the total number of SERA genes differs in different Plasmodium genomes, all those that have been examined to date appear to contain at least one each of the two SERA types (Hodder et al., 2003; McCoubrie et al., 2007).
To further assess the effects of sera types on cell proliferation and population doubling, EBF between passage 3 and 6 were transferred into 6-well plates (2 × 10 cells/cm) and cell numbers were determined manually after day 1, 2, 3, 4, 6 and 8.
Sera, imunoglobulin type, and antigen type were included as covariates.
In view of the well-recognized prevalence of oxidative stress in diabetes mellitus and the susceptibility of calcineurin (Ca2+-calmodulin dependent protein phosphatase 2 B) to free radicals, calcineurin was assayed in the sera of type II diabetic patients.
Sera from type 1 diabetic patients were obtained at disease onset and stored at −20°C until use.
Our study demonstrates that PGRN concentrations and other inflammatory markers, such as TNF- α and IL-6, are markedly elevated in sera of type 2 diabetic patients with microangiopathy.
The monoclonal antibody (Mab -based typing systeMab -basedloped because of typingfficultiesystemuntered wash the use of absorbedevelopedmune polyclonal sera for typing.
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