Magaud J P, Rimokh R, Brochier J, Lafage M, Germain D
Hum Genet. 1985;69(3):238-42. doi: 10.1007/BF00293032.
A monoclonal anti-DNA antibody (HB2) specific for poly dG- poly dC nucleotides was used to stain metaphasic lymphocyte or amniotic cell human chromosomes. HB2 fixation was revealed using either a peroxidase- or a rhodamine-labeled anti-mouse immunoglobulin antiserum. The staining pattern of the chromosomes was dependent on the HB2 concentration: R-banding could be observed at high antibody dilution. Previous trypsinization of metaphasic preparations demonstrated a precise and reproducible typical R-banding independent of the HB2 concentration. This technique appears to be an interesting alternative to other R-banding procedures. The specificity of the antibody allows a better understanding of the biochemical mechanism of R-banding.
一种针对聚dG-聚dC核苷酸的单克隆抗DNA抗体(HB2)被用于对中期淋巴细胞或羊水细胞的人类染色体进行染色。使用过氧化物酶或罗丹明标记的抗小鼠免疫球蛋白抗血清来显示HB2固定情况。染色体的染色模式取决于HB2的浓度:在高抗体稀释度下可观察到R带。对中期制片预先进行胰蛋白酶处理显示出一种精确且可重复的典型R带,且与HB2浓度无关。该技术似乎是其他R带程序的一个有趣替代方法。抗体的特异性有助于更好地理解R带的生化机制。