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Image Search Results
Journal: Reproductive Biology and Endocrinology : RB&E
Article Title: Expressions of candidate molecules in the human fallopian tube and chorionic villi of tubal pregnancy exposed to levonorgestrel emergency contraception
doi: 10.1186/1477-7827-11-46
Figure Lengend Snippet: Primer sequences
Article Snippet:
Techniques:
Journal: Reproductive Biology and Endocrinology : RB&E
Article Title: Expressions of candidate molecules in the human fallopian tube and chorionic villi of tubal pregnancy exposed to levonorgestrel emergency contraception
doi: 10.1186/1477-7827-11-46
Figure Lengend Snippet: Antibody used for immunohistochemistry
Article Snippet:
Techniques: Concentration Assay
Journal: Reproductive Biology and Endocrinology : RB&E
Article Title: Expressions of candidate molecules in the human fallopian tube and chorionic villi of tubal pregnancy exposed to levonorgestrel emergency contraception
doi: 10.1186/1477-7827-11-46
Figure Lengend Snippet: Quantitative real-time PCR analysis of mRNA expression in chorionic villi and the implantation site in fallopian tube of tubal pregnancy. There were no significant differences between the two groups in the mRNA expressions of estrogen receptor (ER)-alpha, progestogen receptor (PR), leukemia inhibitory factor (LIF), vascular endothelial growth factor (VEGF), inducible nitric oxide synthase (iNOS), and endocannabinoid receptor 1 (CB1) in chorionic villi and the implantation site in fallopian tube of tubal pregnancy. All mRNA expression values were normalized against the glyceraldehyde-3-phosphate dehydrogenase (GAPDH) endogenous control gene.
Article Snippet:
Techniques: Real-time Polymerase Chain Reaction, Expressing
Journal: Reproductive Biology and Endocrinology : RB&E
Article Title: Expressions of candidate molecules in the human fallopian tube and chorionic villi of tubal pregnancy exposed to levonorgestrel emergency contraception
doi: 10.1186/1477-7827-11-46
Figure Lengend Snippet: Immunostaining of the chorionic villi in tubal pregnancy. Expressions of estrogen receptor (ER)-alpha ( A, B ), progestogen receptor (PR) ( C, D ), leukemia inhibitory factor (LIF) ( E, F ), vascular endothelial growth factor (VEGF) ( G, H ), inducible nitric oxide synthase (iNOS) ( I, J ) and endocannabinoid receptor (CB1) (K, L) in the chorionic villi observed by immunohistochemistry. Positive staining was detected in the chorionic villi from both the LNG-EC group ( A, C, E, G, I ) and the control group ( B, D, F, H, J ). The immunostaining for ER-alpha ( A, B ) and PR( C, D ) was observed in the nuclei of cytotrophobast, syncytiotrophoblast, and stromal cells from both groups. The immunostaining for LIF ( E, F ), VEGF ( G, H ), iNOS ( I, J ) and CB1 ( K, L ) was seen in the cytoplasm of cytotrophobast, syncytiotrophoblast, and stromal cells from both groups. There were no significant differences between the two groups in the expressions of ER-alpha ( A, B ), PR ( C, D ), LIF ( E, F ), VEGF ( G, H ), iNOS ( I, J ) or CB1 ( K, L ). Magnification: 400×.
Article Snippet:
Techniques: Immunostaining, Immunohistochemistry, Staining
Journal: Reproductive Biology and Endocrinology : RB&E
Article Title: Expressions of candidate molecules in the human fallopian tube and chorionic villi of tubal pregnancy exposed to levonorgestrel emergency contraception
doi: 10.1186/1477-7827-11-46
Figure Lengend Snippet: Immunostaining of the implantation site in the fallopian tube in tubal pregnancy. Representative images showing immunoreactivity of estrogen receptor (ER)-alpha ( A, B ), progestogen receptor (PR) ( C, D ), leukemia inhibitory factor (LIF) ( E, F ), vascular endothelial growth factor (VEGF) ( G, H ), inducible nitric oxide synthase (iNOS) ( I, J ), and endocannabinoid receptor (CB1) ( K, L ). Positive immunolabeling was detected in the epithelial and stromal cells from both the LNG-EC group ( A, C, E, G, I ) and the control group ( B, D, F, H, J ). The immunostaining for ER-alpha ( A, B ) and PR ( C, D ) was observed in the nuclei of the epithelial and stromal cells from both groups. The positive staining for LIF ( E, F ), VEGF ( G, H ), iNOS ( I, J ), and CB1 ( K, L ) was found in the cytoplasm of the epithelial and stromal cells from both groups. No significant differences were observed in any of the immunoreactivity of ER-alpha ( A, B ), PR ( C, D ), LIF ( E, F ), VEGF ( G, H ), iNOS ( I, J ), or CB1 ( K, L ) between the two groups. Magnification: 400×.
Article Snippet:
Techniques: Immunostaining, Immunolabeling, Staining