1.RNAⅢ acts primarily at the level of target gene transcription and independently regulated the transcription of exoprotein. RAP(RNAⅢ activating protein) is a -38KD S. aureus secretory protein which could activate the transcription of RNAⅢ in S. aureus. Now it was found that RAP activated the toxin production via its sensor TRAP (Target of RAP), a membrane-associated -21 kD protein.
其调节过程为RAP蛋白(RNAⅢ activating protein)使其靶分子TRAP蛋白(Target of RAP)磷酸化，从而激活RNAⅢ的转录，上调外毒素的分泌。
2.Homology searches with the deduced 1695 amino acid protein sequence revealed human N-RAP shares 88% similarity with murine N-RAP, 90% with rat N-RAP, 63% with human Nebulin, 58% with rat Nebulin, 60% with chick Nebulin and 59% with murine Nebulin.
小鼠(NP 032759)和大鼠N-RAP蛋白(XP 217637)以及人(NP 004534)、小鼠(AAC52678)、大鼠(XP 229925)和鸡Nebulin蛋白(BAB18734)与人N-RAP一样，均含有多个串联重复的nebulin相关重复序列，相似的序列和结构域组成提示它们同属Nebulin家族。
3.The CDK5RAP1_v3 and CDK5RAP1_v4 cDNAs are 1923bp and 1792bp in length, respectively.
CDK5RAP1_v3和CDK5RAP1_v4的cDNA分别长1923bp和1792bp。
4.ANTI-RAP ANTIBODY-INDUCED RAT GLOMERULAR PODOCYTES RAP GENE EXPRESSION CHANGES IN VITRO
抗RAP抗体对肾小球上皮足突细胞RAP基因表达调控
5.P-RAP method is adopted to grow KBr single crystal. CHBr_3 and the mixture of CH_2Br_2 and CCl_4 are chosen as the P-reagent and RAP-reagent for the purification of KBr raw material and KBr melt respectively. Crucible crack caused by adhesion of the melt can be avoided.
采用P-RAP法生长KBr单晶,用CHBr_3作为纯化固体粉料的试剂,CCl_4与CH_2Br_2的混合物作为纯化KBr熔体的RAP试剂,解决了晶体粘附坩埚引起坩埚的炸裂问题。
6.Cloning and Functional Study of Human Gene C4orf13, CDK5RAP1_v3, CDK5RAP1_v4 and PXK
人类基因C4orf13、CDK5RAP1_v3、CDK5RAP1_v4和PXK的克隆和功能研究
7.Firstly, it narrates the connotation and extension of Rap, and the forms of expression of Pop before Rap.
论及Rap所属Pop的内涵与外延、以及Rap之前的Pop的表现形态;
8.2. PCWP RAP raised bothin CPPA and CPAP while PEEP increased, so PCWP or RAP could not reflect changesin preload exaetly.
2.CPPV和CPAP时PEEP升高,可影响PCWP、RAP(CVP)的准确性。
9.(4) Immunohistochemistry study indicated that in RAP and SC groups, the rate of COX-2 expression was 83.3%(10/12) and 25.0%(3/12) respectively.
(4)RAP组犬心耳内皮细胞COX-2阳性率为83.3％(10／12)，对照组为25.0％(3／12)，RAP组显著高于对照组(p=0.013)；
10.RESULTS After inducing by IPTG, the recombinant RAP protein was expressed characterized by molecular mass about 40KD by SDS-PAGE.
结果 在经IPTG诱导的RAP-pQE30/SG13009全菌蛋白中检测到相对分子量大小约为40KD的RAP重组蛋白,经纯化后明显。
