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METHODS: The different concentrations of natural monoclonal antikeratin antibody IgM 3B4 were incubated with Candida albicans yeast phase suspension on condition that profited germ tube formation of Candida albicans to observe the action of natural monoclonal antikeratin antibody IgM 3B4 to Candida albicans germ tube formation.And the different concentrations of natural monoclonal antikeratin antibody IgM 3B4 were incubated with the mixed suspenions of Candida albicans yeast phase with malpighian cells, human buccal epithelial cells, endothelial cells of fetal umbilical vein, respectively, to observe the action of natural monoclonal antikeratin antibody IgM 3B4 to the adhesion of Candida albicans to malpighian cells, human buccal epithelial cells and endothelial cells of fetal umbilical vein.

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Keratin antibody IgM 3B4 specifically against Candida albicans in vitro. METHODS: The different concentrations of natural monoclonal anti??keratin antibody IgM 3B4 were incubated with Candida albicans yeast phase suspension on condition that profited germ tube formation of Candida albicans to observe the action of natural monoclonal anti??keratin antibody IgM 3B4 to Candida albicans germ tube formation.And the different concentrations of natural monoclonal anti??keratin antibody IgM 3B4 were incubated with the mixed suspenions of Candida albicans yeast phase with malpighian cells, human buccal epithelial cells, endothelial cells of fetal umbilical vein, respectively, to observe the action of natural monoclonal anti??

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METHODS: 24 rabbits were divided into four groups: control group; rapid pacing group; adenosine perfusing group; selective adenosine receptor antagonist perfusing group. The index of observed: time of repolarization in monophase action potential (APD90); the active level of A1 adenosine receptor; the level of free calcium in the atrium cells and the ability of atrium cell to release calcium.

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METHODS: Rat bilateral olfactory bulbs and olfactory mucosa at 1/3 nasal septum were obtained, sliced, digested in trypsin, and made into monoplast suspension. At 1×109/L, cells were incubated in uncoated 25 cm2 culture flask. At 18-20 hours, cell suspension was moved into another uncoated 25 cm2 culture flask (the first differential adhesion). At 24 hours, cell suspension was moved into a poly-D-lysine-coated 25 cm2 culture flask or poly-D-lysine-coated 6-well culture plate (the second differential adhesion). At 48 hours, parenchyma cells were removed after a half of medium was changed.

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Results There were hemodynamic changes of double kidneys in all 120 cases of pregnant women, thereinto, the signs were seen for nephrauxe, hydronephrosis (including 35 cases with hydrops of double kidneys, 12 cases with hydrops of left kidneys ) and sparate collecting system of kidney in various degree in 108 cases, otherwise, there were no visible ultrasonic symptom on hydrops of double kidneys, but low-grade nephrauxe in 12 cases.

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Furthermore,using oxaldehyde,make the emulsion crosslinked and form a kind of net structure,thus a new kind of water-resistant adhesive is created.

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The magnetic properties of carbonyl iron particle s were characterized by VSM;the apparent viscosities and the magnetic field-induced shear stresses of the magnetorheological fluids above were investigated by an advanced rheometric expansion system;the properties of MR damper were tested by an electro-hydralic servocontrol testing system.

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Armigera and M. separata mid-gut juice, but, other less than 60kD proteins also can be got by M. separata mid-gut juice .4 Many Bt Cry1AcE toxins can be got by the method of precipitate and resolve, which have high purity.

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2 The analysis step by 125mL separatory funnel, a fartoo 0.1mL cadmiun forcultivation added liquid (equivalent 1 μ g cadmiun) and 50mL acetate (4%), and the other one is to join the 50.0mL sample lixivium, separatory funnel and 2mL in the seignette solution,-amoxycillin sodium hydroxide solution and potassium cyanide-2mL hydroxylammonium hydrochloride solution, each adding a reagent shake after.

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