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antibsa
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  anti-bsa
     The results showed that the home svnthesized TTA-SO_2Cl was a suc cessful bifunctional ligand,high conjugation ratios(TTA:BSA = 35:1,TTA:anti-BSA=100:1)were obtained.
     研究结果表明TTA-SO_2O是一种标记效率较高的双功能络合剂,可获得较高的结合比(TTA:BSA=35:1;TTA:anti-BSA=100:1)。
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     while CSF anti N is sensitive and specific for CNS SLE,and anti N level is associated with disease activity of CNS SLE.
     脑脊液中anti N是
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     Study on synthesis of swainsonine-BSA
     苦马豆素-BSA的合成研究
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     THE SYNTHESIS OF CORTICOSTERONE-3-BSA
     皮质酮-3-BSA的合成
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     Anti-Fuzzy Subgroup′s Homomorphism
     Anti-Fuzzy子群的同态
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     STUDY ON EQUILIBRIUM DIALYSIS OF Hg(Ⅱ) BINDING TO BSA
     Hg(Ⅱ)BSA的平衡透析研究
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  antibsa
Methotrexate (MTX) was first conjugated to antibovine serum albumin IgG (antiBSA) or its F(ab)2 fragment to define conditions for retention of drug and antibody activity.
      
With identical drug: protein molar ratios, incorporation in the F(ab)2 fragment was lower than in intact antiBSA, an observation consistent with analysis of the number of lysine residues (22 in F(ab)2 compared to 40 in antiBSA).
      
At an incorporation ratio of 6 mol MTX per mol protein, MTX-antiBSA retained 100% of antibody activity and MTX-F(ab)2antiBSA retained 75%.
      
MTX-antiBSA and MTX-F(ab)2antiBSA were equally potent in vitro inhibitors of dihydrofolate reductase.
      
On the other hand, superoxide generation enhancing activity of BSA-antiBSA immune complexes was not affected by preincubation with rheumatoid factors isolated from the sera of either rheumatoid arthritits patients or the macroglobulinemia patient.
      
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The noncompetitive capillary electrophoresis based immunoassay for proteins using bovine serum albumin (BSA)and its monoclonal antibody (anti-BSA)as a model system were studied.BSA was labeled with fluorescein isothiocyanate and used as a tracer to determine anti-BSA.The binding reaction between antiBSA and the tracer reached equilibrium in less than 20 minutes,and separation between the immunocomplexes and the free tracer was achieved in 12 minutes using capillary zone electrophoresis.The linear dynamic...

The noncompetitive capillary electrophoresis based immunoassay for proteins using bovine serum albumin (BSA)and its monoclonal antibody (anti-BSA)as a model system were studied.BSA was labeled with fluorescein isothiocyanate and used as a tracer to determine anti-BSA.The binding reaction between antiBSA and the tracer reached equilibrium in less than 20 minutes,and separation between the immunocomplexes and the free tracer was achieved in 12 minutes using capillary zone electrophoresis.The linear dynamic range of the standard curve was 8~150 nmol/L,and the detection limit was 5nmol/L when a tracer concentration of 320 nmol/L was used.Influences of separation conditions such as buffer concentration,pH and separation voltage was also studied.

以牛血清白蛋白与其单克隆抗体为样品,初步研究了蛋白质的非竞争性毛细管电泳免疫分析方法。混合温育可以在对20min内达到平衡,电泳分离在12min内完成。当示踪物浓度为320nmol/L时,所得到的标准曲线的线性范围为8-150nmol/L,检出限为5nmol/L,并考察了缓冲溶液的浓度、pH、分离电压等因素的影响。

 
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