| 1. | Mpges immunostaining was strongly detected on day 5 after birth
Mpges免疫染色自出生5日后在颗粒细胞中很强。 |
| 2. | Mpges mrna and protein were not detected in the pseudopregnant uterus from days 1 to 8
在妊娠第1天小鼠子宫中没有检测到mpges的免疫染色。 |
| 3. | A low level of cpges immunostaining was detected in oocyte cytoplasm on day 5 after birth
5日龄小鼠的卵巢中，卵母细胞质中有较弱的cpges免疫染色。 |
| 4. | Cpges mrna signal was maily located in oocyte cytoplasm and declined at 48 h after pmsg treatment
在pmsg处理后的卵泡颗粒细胞中，几乎检测不到cpges免疫染色。 |
| 5. | Then cpges immunostaining gradually decreased and reached to a basal level in adult ovary
以后，卵母细胞质中的cpges免疫染色逐步减弱，在成体卵母细胞质中很弱。 |
| 6. | The basal cell layer is fragmented but still present as confirmed by high molecular weight cytokeratin immunostain ( next slide )
基底细胞层已成碎片，但是通过高分子量细胞角蛋白免疫染色后仍可确定其存在（见下一张） 。 |
| 7. | After stained , lpo was detected in the immunohistochemical background . and area x could be distinguished from the surrounding lpo
经免疫染色后， lpo界限明显，并在lpo中基本能识别出x区，但有些个体的x区并不明显。 |
| 8. | In contrast , ep2 immunostaining was strong in the luminal epithelium and glandular epithelium under delayed implantation and reinitiation of implantation
在第6 - 9天的子宫蜕膜区和胚胎上， ep2免疫染色较弱或检测不到。 |
| 9. | The diagnosis of superficial acral fibromyxoma was made by the clinical and histopathological features , together with the immunostaining results
就临床、组织病理学的特徵及免疫染色的结果而言，可符合一表浅性肢端纤维黏液瘤之诊断。 |
| 10. | On day 10 after birth , the staining in oocyte cytoplasm was stronger , while the staining became weaker again on day 15 . the strongest cpges immunostaining was seen on day 20
10日龄小鼠卵巢卵母细胞质中， cpges的免疫染色较强，但在15日龄小鼠卵巢卵母细胞质中又转弱。 |
