493 research outputs found
Comparison of Spider-Robot Information Models
The paper deduces a mathematical model of a spider-robot with six three-link limbs. Many limbs with a multi-link structure greatly complicate the process of synthesizing a model, since in total the robot has twenty-four degrees of freedom, i.e., three coordinates of the center of mass of the body in space, three angles of rotation of the body relative to its center of mass and three degrees of freedom for each limb, to describe the position of the links. The derived mathematical model is based on the Lagrange equations with a further transformation of the equations to the Cauchy normal form in a matrix form. To test the resulting model in a SimInTech environment, an information model is synthesized and two simple experiments ar carried out to simulate the behavior of real spiders: moving forward in a straight line and turning in place at a given angle. The experimental results demonstrate that the synthesized information model can well cope with the tasks and the mathematical model underlying it can be used for further research
TREC and KREC Levels as a Predictors of Lymphocyte Subpopulations Measured by Flow Cytometry
Primary immunodeficiency diseases (PID) is a heterogeneous group of disorders caused
by genetic defects of the immune system, which manifests clinically as recurrent
infections, autoimmune diseases, or malignancies. Early detection of other PID remains
a challenge, particularly in older children due to milder and less specific symptoms,
a low level of clinician PID awareness and poor provision of hospital laboratories
with appropriate devices. T-cell recombination excision circles (TREC) and kappadeleting element recombination circle (KREC) in a dried blood spot and in peripheral
blood using real-time polymerase chain reaction (PCR) are used as a tool for severe
combined immune deficiency but not in PID. They represent an attractive and cheap
target for a more extensive use in clinical practice. This study aimed to assess
TREC/KREC correspondence with lymphocyte subpopulations, measured by flow
cytometry and evaluate correlations between TREC/KREC, lymphocyte subpopulations
and immunoglobulins. We carried out analysis of data from children assessed by clinical
immunologists at Speransky Children’s Hospital, Moscow, Russia with suspected
immunodeficiencies between May 2013 and August 2016. Peripheral blood samples
were sent for TREC/KREC, flow cytometry (CD3, CD4, CD8, and CD19), IgA, IgM, and
IgG analysis. A total of 839 samples were analyzed for using TREC assay and flow cytometry and 931 KREC/flow cytometry. TREC demonstrated an AUC of 0.73 (95% CI
0.70–0.76) for CD3, 0.74 (95% CI 0.71–0.77) for CD4 and 0.67 (95% CI 0.63–0.70) for
CD8, respectively, while KREC demonstrated an AUC of 0.72 (95% CI 0.69–0.76) for
CD19. Moderate correlation was found between the levels of TREC and CD4 (r = 0.55,
p < 0.01) and KREC with CD19 (r = 0.56, p < 0.01). In this study, promising prediction
models were tested. We found that TREC and KREC are able to moderately detect
abnormal levels of individual lymphocyte subpopulations. Future research should assess
associations between TREC/KREC and other lymphocyte subpopulations and approach
TREC/KREC use in PID diagnosis
Development of Wolffia arrhiza as a Producer for Recombinant Human Granulocyte Colony-Stimulating Factor
To date, the expression of recombinant proteins in transgenic plants is becoming a powerful alternative to classical expression methods. Special efforts are directed to the development of contained cultivation systems based on cell culture or rhyzosecretion, which reliably prevents the heterologous DNA releasing into the environment. A promising object for the development of such systems is the tiny aquatic plant of Wolffia arrhiza, which can be used as a dipped culture in bioreactors. Herein we have expressed the human granulocyte colony-stimulating factor (hG-CSF) in nuclear-transformed Wolffia. The nucleotide sequence of hG-CSF was optimized for expression in Wolffia and cloned into the vector pCamGCSF downstream of double CaMV 35S promoter. Wolffia plants were successfully transformed and 34 independent transgenic lines with hG-CSF gene were obtained, PCR and Southern blot analysis confirmed the transgenic origin of these lines. Western blot analysis revealed accumulation of the target protein in 33 transgenic lines. Quantitative ELISA of protein extracts from these lines showed hG-CSF accumulation up to 35.5 mg/kg of Wolffia fresh weight (0.194% of total soluble protein). This relatively high yield holds promise for the development of Wolffia-based expression system in strictly controlled format to produce various recombinant proteins
METHOD OF NANO-CRYSTALLINE ALLOY RECEIVING
FIELD: metallurgy. SUBSTANCE: it is implemented melting of alloy in capsule, then melt is pressed out through the hole in capsule on surface of rotating cooling disc with passing of constant current through the stream of melt and cooling disc at that changing of cooling rate of melt on cooling disc while passing of current is implemented by means of matching of current density value and directing of its behavior for forming of nano-structural condition of alloy with required grain size and its minimal dispersion. EFFECT: uniform nano-structure in alloy, maximal service properties. 1 tbl, 5 dwg.Изобретение относится к области металлургии и может быть использовано при производстве нанокристаллических материалов в виде ленты. Для получения необходимой однородной наноструктуры в сплаве, обеспечивающей его максимальные служебные свойства, осуществляют плавление сплава в тигле, затем расплав выдавливают через отверстие в тигле на поверхность вращающегося охлаждающего диска с пропусканием постоянного электрического тока через струю расплава и охлаждающий диск, при этом изменение скорости охлаждения расплава на охлаждающем диске при пропускании тока ведут путем подбора величины плотности тока и направления его протекания для формирования наноструктурного состояния сплава с требуемым размером зерна и его минимальной дисперсией. 1 з.п.ф-лы, 1 табл., 5 ил
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