rabbit polyclonal anti cb2 Search Results


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Bioss cnr2 cb2 polyclonal antibody
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GeneTex primary rabbit polyclonal anti cb 2 receptor antibody (rrid:ab_374359)
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Cayman Chemical rabbit anti-human cb 2 r polyclonal antibody cayman chemicals, ann arbor, mi
Primer sequences
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Alpha Diagnostics polyclonal rabbit anti- human-cb2 antibody
Primer sequences
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Alpha Diagnostics affinity-purified polyclonal rabbit anti-human-cb2 antibody
Primer sequences
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Cayman Chemical rabbit polyclonal anti-human cb2 antibody lot 136802
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Image Search Results


Primer sequences

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: CB1 , Enzo Life Sciences International USA , 1:150 , From rabbit , EDTA solution , microwave heating on high for 20 minutes.

Techniques:

Antibody used for immunohistochemistry

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: CB1 , Enzo Life Sciences International USA , 1:150 , From rabbit , EDTA solution , microwave heating on high for 20 minutes.

Techniques: Concentration Assay

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.

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: CB1 , Enzo Life Sciences International USA , 1:150 , From rabbit , EDTA solution , microwave heating on high for 20 minutes.

Techniques: Real-time Polymerase Chain Reaction, Expressing

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×.

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: CB1 , Enzo Life Sciences International USA , 1:150 , From rabbit , EDTA solution , microwave heating on high for 20 minutes.

Techniques: Immunostaining, Immunohistochemistry, Staining

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×.

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: CB1 , Enzo Life Sciences International USA , 1:150 , From rabbit , EDTA solution , microwave heating on high for 20 minutes.

Techniques: Immunostaining, Immunolabeling, Staining