scholarly journals Monoclonal antibody to chicken oviduct progesterone receptor.

1983 ◽  
Vol 80 (10) ◽  
pp. 2854-2858 ◽  
Author(s):  
C. Radanyi ◽  
I. Joab ◽  
J. M. Renoir ◽  
H. Richard-Foy ◽  
E. E. Baulieu
Keyword(s):  
Monoclonal Antibody ◽  
Progesterone Receptor ◽  
Chicken Oviduct

A monoclonal antibody produced against the chicken oviduct progesterone receptor shows cross reaction with human antigen

1984 ◽  
Vol 20 (6) ◽  
pp. 1627 ◽  
Author(s):  
D. Edwards ◽  
W. McGuire ◽  
N. Weigel ◽  
W. Schrader ◽  
B. O'Malley
Keyword(s):  
Monoclonal Antibody ◽  
Progesterone Receptor ◽  
Cross Reaction ◽  
Chicken Oviduct

scholarly journals Phosphorylation in vivo of chicken oviduct progesterone receptor.

1982 ◽  
Vol 257 (23) ◽  
pp. 14226-14230
Author(s):  
J J Dougherty ◽  
R K Puri ◽  
D O Toft
Keyword(s):  
Progesterone Receptor ◽  
Chicken Oviduct

Characterization of a novel 23-kilodalton protein of unactive progesterone receptor complexes

1994 ◽  
Vol 14 (3) ◽  
pp. 1956-1963
Author(s):  
J L Johnson ◽  
T G Beito ◽  
C J Krco ◽  
D O Toft
Keyword(s):  
Progesterone Receptor ◽  
Cdna Clone ◽  
Peptide Fragments ◽  
Receptor Complexes ◽  
Human Cdna ◽  
Partial Clone ◽  
Chicken Oviduct ◽  
Brain Cdna Library ◽  
Carboxy Terminal ◽  
And Function

Immunoprecipitation of unactivated avian progesterone receptor results in the copurification of hsp90, hsp70, and three additional proteins, p54, p50, and p23. p23 is also present in immunoaffinity-purified hsp90 complexes along with hsp70 and another protein, p60. Antibody and cDNA probes for p23 were prepared in an effort to elucidate the significance and function of this protein. Antibodies to p23 detect similar levels of p23 in all tissues tested and cross-react with a protein of the same size in mice, rabbits, guinea pigs, humans, and Saccharomyces cerevisiae, indicating that p23 is a conserved protein of broad tissue distribution. These antibodies were used to screen a chicken brain cDNA library, resulting in the isolation of a 468-bp partial cDNA clone encoding a sequence containing four sequences corresponding to peptide fragments isolated from chicken p23. This partial clone was subsequently used to isolate a full-length human cDNA clone. The human cDNA encodes a protein of 160 amino acids that does not show homology to previously identified proteins. The chicken and human cDNAs are 88% identical at the DNA level and 96.3% identical at the protein level. p23 is a highly acidic phosphoprotein with an aspartic acid-rich carboxy-terminal domain. Bacterially overexpressed human p23 was used to raise several monoclonal antibodies to p23. These antibodies specifically immunoprecipitate p23 in complex with hsp90 in all tissues tested and can be used to immunoaffinity isolate progesterone receptor complexes from chicken oviduct cytosol.

scholarly journals Progesterone receptor in the chick oviduct: an immunohistochemical study with antibodies to distinct receptor components.

1984 ◽  
Vol 99 (4) ◽  
pp. 1193-1201 ◽  
Author(s):  
J M Gasc ◽  
J M Renoir ◽  
C Radanyi ◽  
I Joab ◽  
P Tuohimaa ◽  
...  
Keyword(s):  
Progesterone Receptor ◽  
Polyclonal Antibodies ◽  
Smooth Muscles ◽  
Immunoperoxidase Technique ◽  
Cell Nuclei ◽  
Receptor Complexes ◽  
B Subunit ◽  
Chicken Oviduct ◽  
A Subunit ◽  
Immunohistochemical Studies

We performed immunohistochemical studies of chicken oviduct after different fixation procedures, by using antibodies against the progesterone receptor: polyclonal antibodies IgG-G3 against the "8S" form (an oligomere containing progesterone-binding and nonprogesterone-binding units), polyclonal antibodies IgG-RB against the progesterone-binding B subunit, and monoclonal BF4 against the non-progesterone-binding 90,000-mol-wt protein component. Chickens were immature animals with or without estrogen priming, and with or without progesterone treatment. The antibodies were revealed by means of an immunoperoxidase technique that used the avidin-biotin-peroxidase complex, and controls were performed by presaturation of antibodies with the purified 8S-progesterone receptor, the B subunit, and 90,000-mol-wt protein. The progesterone receptor was detected not only in well-characterized target tissues, i.e., in glands and luminal epithelium, but also in stromal cells (some displayed the strongest reaction), in mesothelium, and in fibers of smooth muscles. Only in cell nuclei, whether or not the animals received an injection of progesterone was an antigen revealed corresponding to the B subunit (and/or to the A subunit, because there is immunoreactivity of IgG-RB with both hormone-binding subunits A and B). The 90,000-mol-wt protein was revealed in both cytoplasm and nuclei. These immunohistological data suggest that the concept of steroid action that necessarily involves the original formation of the hormone-receptor complexes in the cytoplasm before translocation to the nucleus, may have to be revised.

Structural analysis of chicken oviduct progesterone receptor using monoclonal antibodies to the subunit B protein

Biochemistry ◽  
1984 ◽  
Vol 23 (19) ◽  
pp. 4427-4435 ◽  
Author(s):  
Dean P. Edwards ◽  
Nancy L. Weigel ◽  
William T. Schrader ◽  
Bert W. O'Malley ◽  
William L. McGuire
Keyword(s):  
Monoclonal Antibodies ◽  
Structural Analysis ◽  
Progesterone Receptor ◽  
Chicken Oviduct ◽  
Subunit B

scholarly journals Immunohistochemical studies on the progesterone receptor (PR) in the sow uterus during the oestrous cycle and in inseminated sows at oestrus and early pregnancy

Reproduction ◽  
2005 ◽  
Vol 129 (3) ◽  
pp. 349-359 ◽  
Author(s):  
S Sukjumlong ◽  
A-M Dalin ◽  
L Sahlin ◽  
E Persson
Keyword(s):  
Monoclonal Antibody ◽  
Progesterone Receptor ◽  
Early Pregnancy ◽  
Artificial Insemination ◽  
Oestrous Cycle ◽  
Surface Epithelium ◽  
Physiological Changes ◽  
Receptor Proteins ◽  
High Level ◽  
Immunohistochemical Studies

Physiological changes in the sow uterus involve the regulation by progesterone and its receptor proteins (PR). Therefore, the aim of the present study was to investigate the localization of PR during different stages of the oestrous cycle and in inseminated sows during early pregnancy by use of immunohistochemistry. Uterine samples were collected from cyclic and inseminated sows at different stages of the oestrous cycle and early pregnancy. The samples were fixed in 10% formaldehyde and embedded in paraffin. Immunohistochemistry was done by use of a mouse monoclonal antibody to PR. The highest PR immunostaining in the surface epithelium was observed at oestrus/5–6 h after artificial insemination (AI) and early dioestrus/70 h after AI. In the glandular epithelium, the highest level of PR was found at oestrus with the lowest at late dioestrus/d 19. Higher levels of PR were observed in inseminated groups compared with cyclic sows. In the myometrium, a high level of PR was found at oestrus, while stromal PR cells were constantly present throughout the oestrous cycle and at different stages of early pregnancy. In conclusion, this study shows that the immunopresence of PR in the sow uterus differed between uterine compartments at the same reproductive stage. Differences were also found for some uterine compartments between cyclic and inseminated/early pregnant sows. The relatively consistent immunostaining of PR in the stroma strengthens a stromal role in the regulation of physiological activities in the sow uterus during the oestrous cycle as well as early pregnancy.

scholarly journals Expression of Progesterone Receptors in Hippocampal Neurons in Rabbit Males

2012 ◽  
Vol 56 (2) ◽  
pp. 231-234
Author(s):  
Izabela Krakowska ◽  
Grzegorz Lonc
Keyword(s):  
Monoclonal Antibody ◽  
New Zealand ◽  
Progesterone Receptor ◽  
Hippocampal Neurons ◽  
Progesterone Receptors ◽  
Direct Influence ◽  
Immunohistochemical Detection ◽  
Granular Cells

Abstract The aim of this study was to investigate the presence of progesterone receptors in hippocampal neurons of male rabbits and the distribution of these receptors in different areas of the hippocampus. The examinations were carried out on brains of five males, New Zealand breed, age of 2 years, weighing 2-3 kg. Immunohistochemical detection of receptors was performed using DAKO LSAB + Kit Peroxidase method. The sections were incubated with primary monoclonal antibody for progesterone receptor NCL-LPGR- AB. The obtained results have shown the presence of progesterone receptors in neurons of CA1, CA3, and CA4 regions of the hippocampus. The reaction also occurred in the region of granular cells of the dental gyrus. The reaction was seen in the cytoplasm and nuclei of neurons simultaneously, whereas some neurons did not show any reaction in the nucleus and cytoplasm. Occurrence of progesterone receptors in most neurons of the hippocampus confirms a direct influence of progesterone on the hippocampus and its functions in rabbit males.

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