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Stalling protection start

Stalling or locked rotor protection. This is also detected by the prolonged starting time as well as overheating of the machine. It is possible that the machine was already under operation and hot when it had stalled. Under such a condition, the rotor operates at a high freqitency and is more vulnerable to damage. Since it is not possible to create a replica of the rotor, separate... [Pg.297]

To ensure a time long enough to disconnect the motor from its power supply when the motor is stalled, fE shall exceed 5 s. When current dependent protective devices are applied to initiate the disconnection, fE shall increase with decreasing ratios of starting current to rated current. [Pg.204]

Figure 5 Starting from natural mRNA, a cDNA library (A blue) is produced and like ribosomal display, the cDNA is transcribed into mRNA (B) with no stop codons. The 3 -end of each mRNA molecule is ligated to a short synthetic DNA linker (C) and sometimes a polyethyleneglycol spacer, which terminates with a puramycin molecule (small red sphere). The ligation is stabilized by the addition of psoralen (green clamp), which is photoactivated to covalently join both strands. Addition of crude polysomes or purified ribosomes (D) results in translation of the mRNA into protein, but the ribosome stalls at the mRNA-DNA junction. Since there are no stop codons, release factors cannot function and instead the puromycin enters the A-site of the ribosome (A). Because puramycin is an analog of tyrosyl-tRNA, the peptidyl transferase subunit catalyzes amide bond formation between the puromycin amine and the peptide carboxyl terminus, but is unable to hydrolyze the amide link (which should be an ester in tyrosyl-tRNA) to release the dimethyladenosine. The ribosome is dissociated to release the mRNA-protein fusion (E), which is protected with complementary cDNA using RT-PCR (F). The mRNA library can then be selected against an immobilized natural product probe (G), nonbinding library members washed away and the bound mRNA (H) released with SDS. PCR amplification of the cDNA provides a sublibrary (A) for another round of selection or for analysis/ sequencing. Figure 5 Starting from natural mRNA, a cDNA library (A blue) is produced and like ribosomal display, the cDNA is transcribed into mRNA (B) with no stop codons. The 3 -end of each mRNA molecule is ligated to a short synthetic DNA linker (C) and sometimes a polyethyleneglycol spacer, which terminates with a puramycin molecule (small red sphere). The ligation is stabilized by the addition of psoralen (green clamp), which is photoactivated to covalently join both strands. Addition of crude polysomes or purified ribosomes (D) results in translation of the mRNA into protein, but the ribosome stalls at the mRNA-DNA junction. Since there are no stop codons, release factors cannot function and instead the puromycin enters the A-site of the ribosome (A). Because puramycin is an analog of tyrosyl-tRNA, the peptidyl transferase subunit catalyzes amide bond formation between the puromycin amine and the peptide carboxyl terminus, but is unable to hydrolyze the amide link (which should be an ester in tyrosyl-tRNA) to release the dimethyladenosine. The ribosome is dissociated to release the mRNA-protein fusion (E), which is protected with complementary cDNA using RT-PCR (F). The mRNA library can then be selected against an immobilized natural product probe (G), nonbinding library members washed away and the bound mRNA (H) released with SDS. PCR amplification of the cDNA provides a sublibrary (A) for another round of selection or for analysis/ sequencing.
Are disconnecting switches for electrical motors in excess of 2hp capable of opening the circuit when the motor is in a stalled condition, without exploding (Switches must be horsepower rated equal to or in excess of the motor hp rating.) Is low-voltage protection provided in the control device of motors driving machines or equipment that could cause probable injury from inadvertent starting ... [Pg.386]


See other pages where Stalling protection start is mentioned: [Pg.283]    [Pg.295]    [Pg.302]    [Pg.44]    [Pg.199]    [Pg.287]    [Pg.291]    [Pg.308]    [Pg.273]    [Pg.125]    [Pg.340]    [Pg.47]    [Pg.641]    [Pg.378]    [Pg.649]    [Pg.555]   
See also in sourсe #XX -- [ Pg.43 ]




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