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235 results about "Initial cell" patented technology

Method and mobile station to perform the initial cell search in time slotted systems

A method is disclosed that a Mobile Station MS performs at switch-on to search the most favorable target cell in UMTS systems like the 3GPP CDMA—LCR (Low Chip Rate) option at 1.28 Mcps—TDD (Time Division Duplex) mode and the equivalent TD-SCDMA (Time Division—Synchronous CDMA). Signal at the MS antenna is the sum of different RF downlink frames coming from different carriers in the assigned frequency ranges. A DL synchronization timeslot and a BCCH TS0 are both transmitted with full power in the frames, the first one includes one out of 32 SYNC codes assigned on cell basis. Following a conventional approach the absence of a common downlink pilot and without prior knowledge of the used frequencies would force the MS, for all the frequencies of the channel raster stored in the SIM card, the correlation of the received frame with all the 32 SYNCs stored in the MS, in order to detect the BSIC of a cell to which associate the power measures. Following the two-step method of the invention the power measures are performed in two-step scan of the PLMN band without interleaved correlation steps; once a final frequency is selected the respective frame is the only correlated one. At least one frame duration about 5 ms long of the whole 15 MHz bandwidth is acquired, IF converted, A/D converted and the digital set is stored. A rough scan is performed multiplying the digital set by a digital IF tuned in steps wide as the channel band (1.6 MHz) along the 15 MHz band, and filtering the baseband signal with a Root Raise Cosine low-pass filter. The 5 ms baseband signal is subdivided into 15 blocks of half timeslot (337.5 μs) and the power of each block is measured. The power of the strongest block indicates the priority of the respective frequency. The strongest power values are put in a Spectral Table together with respective frame load indicators. The load indicator is the percentage of timeslots in a frame almost equally loaded as the strongest block. The three strongest frequencies are selected for the successive scan. The second step search is performed like the first one but the IF steps are now 200 kHz wide and cover the only 1.6 MHz spectrum around a selected frequency. A final frequency is selected for the successive correlation step. Then the frequency error of the MS reference oscillator is corrected with data-aided techniques and a calibration value stored for successive connections (FIG. 9).
Owner:SIEMENS INFORMATION & COMM NEWTWORKS INC

Product quality enhancement in mammalian cell culture processes for protein production

The present invention describes methods and processes for the production of proteins, particularly glycoproteins, by animal cell or mammalian cell culture, illustratively, but not limited to, fed-batch cell cultures. The methods comprise feeding the cells with D-galactose, preferably with feed medium containing D-galactose, preferably daily, to sustain a sialylation effective level of D-galactose in the culture for its duration, thus increasing sialylation of the produced proteins. The methods can also comprise at least two temperature shifts performed during the culturing period, in which the temperature is lower at the end of the culturing period than at the time of initial cell culture. The cell culture processes of the invention involving two or more temperature shifts sustain a high cell viability, and can allow for an extended protein production phase. The methods can also comprise the delayed addition of polyanionic compound at a time after innoculation. Supplementation of the cultures with D-galactose, preferably in a feed medium, to sustain galactose at sialylation effective levels in the cultures until the end of a culture run reverses a decline in sialylation that accompanies culture scale up, and is advantageous for large scale culturing processes.
Owner:BRISTOL MYERS SQUIBB CO

Polypeptide production in animal cell culture

A method of producing a polypeptide in fed batch cell culture is provided which involves an initial cell growth phase and a distinct production phase. In the initial growth stage, animal cells having nucleic acid encoding the polypeptide are cultured at a starting osmolality of about 280-330 mOsm in the presence of a concentration of glucose controlled throughout the culturing to be within a range between about 0.01 and 1 g/L. This is followed by a production phase, where the cultured animal cells of the growth phase are inoculated at a cell seed density of at least 1.0×106 cells/mL and the cells are cultured at a starting osmolarity of about 400-600 mOsm in the presence of a concentration of glucose controlled throughout the culturing to be within a range between about 0.01 and 1 g/L. Preferably, the glutamine concentration in the cell culture medium is simultaneously controlled in order to curtail production of lactic acid and ammonia which result from unnecessarily high glutamine concentrations. During the growth phase, production of potentially detrimental metabolic waste products, such as lactic acid, is controlled thereby curtailing the increase of osmolality due to accumulation and neutralization of waste products. Thus, the cell growth can be improved. In the production phase, the cell culture conditions are modified in order to arrest or reduce cell growth and thereby direct nutrient utilization toward production, as opposed to cell growth. Overall, it is intended that the method results in an improvement in specific productivity, reduction in production run times and/or an increase in final product concentration.
Owner:GENENTECH INC

Product quality enhancement in mammalian cell culture processes for protein production

The present invention describes methods and processes for the production of proteins, particularly glycoproteins, by animal cell or mammalian cell culture, illustratively, but not limited to, fed-batch cell cultures. The methods comprise feeding the cells with D-galactose, preferably with feed medium containing D-galactose, preferably daily, to sustain a sialylation effective level of D-galactose in the culture for its duration, thus increasing sialylation of the produced proteins. The methods can also comprise at least two temperature shifts performed during the culturing period, in which the temperature is lower at the end of the culturing period than at the time of initial cell culture. The cell culture processes of the invention involving two or more temperature shifts sustain a high cell viability, and can allow for an extended protein production phase. The methods can also comprise the delayed addition of polyanionic compound at a time after innoculation. Supplementation of the cultures with D-galactose, preferably in a feed medium, to sustain galactose at sialylation effective levels in the cultures until the end of a culture run reverses a decline in sialylation that accompanies culture scale up, and is advantageous for large scale culturing processes.
Owner:BRISTOL MYERS SQUIBB CO

Method and system for encoding wide striped cells

A system and method for encoding wide striped cells that carry packets of data across stripes. The method encodes an initial block of a first wide striped cell is encoded with initial cell encoding information, and distributes initial bytes of packet data into available space in the initial block of the first wide striped cell. The initial cell encoding information includes control information and state information. One initial block of the first wide striped cell comprises five subblocks corresponding to five stripes. Each subblock includes identical control information and identical state information. The method further includes adding reserve information to available bytes at the end of the initial block of the first wide striped cell. Remaining bytes of packet data are distributed across one or more blocks in the first wide striped cell until an end of packet condition is reached or a maximum cell size is reached. Other steps include encoding the first wide striped cell or another wide striped cell with end of packet information. The end of packet information varies depending upon a set of end of packet conditions, such as, whether the end of packet occurs at the end of an initial block, at the end of the initial block, within a subsequent block, at a block boundary, or at a cell boundary.
Owner:AVAGO TECH INT SALES PTE LTD

SOC estimation method and SOC estimation device based on cell characteristic curve

ActiveCN106772072AAchieve correctionEstimate method is simple and feasibleElectrical testingEngineeringSimple computation
The invention discloses an SOC estimation method and an SOC estimation device based on a cell characteristic curve, wherein the SOC estimation method and the SOC estimation device belong to the field of cell management and testing technology. The SOC estimation method comprises the steps of acquiring an initial cell state-of-charge, a cell capacity, a cell monomer voltage value, a cell monomer temperature value, a cell working current value and a cell sampling period; performing calculation for obtaining a first cell state-of-charge; when duration time in which the cell working current value is smaller than a current threshold is shorter than a time threshold, obtaining a second cell state-of-charge according to preset state-of-charge-open-circuit-voltage curves at different temperatures; calculating a difference between the first cell state-of-charge and the second cell state-of-charge, and calculating the absolute value of the difference, thereby obtaining the cell state-of-charge difference; and determining a relationship between the cell state-of-charge difference and a state-of-charge threshold for determining a final cell state-of-charge. The SOC estimation method and the SOC estimation device have advantages of satisfying a requirement for high SOC testing precision at different temperatures by means of a simple calculation process, realizing SOC estimation and correction, and ensuring convenient and feasible calculation method and wide application range.
Owner:CHERY AUTOMOBILE CO LTD
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