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anti-Human Progesterone Receptor Antibodies:
anti-Mouse (Murine) Progesterone Receptor Antibodies:
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Human Monoclonal Progesterone Receptor Primary Antibody for ELISA, WB - ABIN969352
Saito, Ito, Nagase, Suzuki, Akahira, Okamura, Yaegashi, Sasano: Progesterone receptor isoforms as a prognostic marker in human endometrial carcinoma. in Cancer science 2006
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Human Monoclonal Progesterone Receptor Primary Antibody for ChIP, ICC - ABIN2668242
Rochette-Egly, Lutz, Pfister, Heyberger, Scheuer, Chambon, Gaub: Detection of retinoid X receptors using specific monoclonal and polyclonal antibodies. in Biochemical and biophysical research communications 1994
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Human Polyclonal Progesterone Receptor Primary Antibody for WB - ABIN1881649
Van Belle, Van Calster, Brouckaert, Vanden Bempt, Pintens, Harvey, Murray, Naume, Wiedswang, Paridaens, Moerman, Amant, Leunen, Smeets, Drijkoningen, Wildiers, Christiaens, Vergote, Van Huffel, Neven: Qualitative assessment of the progesterone receptor and HER2 improves the Nottingham Prognostic Index up to 5 years after breast cancer diagnosis. in Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2010
Show all 3 Pubmed References
Human Polyclonal Progesterone Receptor Primary Antibody for WB - ABIN1881650
Geradts, Bean, Bentley, Barry: The oncotype DX recurrence score is correlated with a composite index including routinely reported pathobiologic features. in Cancer investigation 2010
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Human Monoclonal Progesterone Receptor Primary Antibody for IF, IHC (p) - ABIN562204
Liu, Chang, Kuo, Hwa, Lin, Huang, Chen, Chang, Hsieh: Major Functional Transcriptome of an Inferred Center Regulator of an ER(-) Breast Cancer Model System. in Cancer informatics 2012
Show all 2 Pubmed References
Human Monoclonal Progesterone Receptor Primary Antibody for ELISA, WB - ABIN966829
Polo, José Galindo, Martínez, Alvarez, Arévalo, Asensi, Cánoves, Cáncer, Collazos, Estrada, Gómez-Candela, Johnston, Locutura, López-Aldeguer, Lozano, Miralles, Muñoz-Sanz, Ortega, Pascua, Pedrol, Pulido, San Martín, Sanz, Viciana, Chamorro,: [Recommendations of the Study Group for Metabolic Alterations/Secretariat for the National AIDS Plan (GEAM/SPNS) on the management of metabolic and morphologic alterations in patients with HIV infection]. in Enfermedades infecciosas y microbiología clínica 2006
Show all 4 Pubmed References
Human Monoclonal Progesterone Receptor Primary Antibody for ELISA - ABIN1724699
Tung, Abdel-Hafiz, Shen, Harvell, Nitao, Richer, Sartorius, Takimoto, Horwitz: Progesterone receptors (PR)-B and -A regulate transcription by different mechanisms: AF-3 exerts regulatory control over coactivator binding to PR-B. in Molecular endocrinology (Baltimore, Md.) 2006
Show all 2 Pubmed References
Human Monoclonal Progesterone Receptor Primary Antibody for IHC (fro), IHC - ABIN152361
Pérez, Cuadros, Benítez, Jiménez: Interaction of Alzheimer's disease amyloid beta peptide fragment 25-35 with tau protein, and with a tau peptide containing the microtubule binding domain. in Journal of Alzheimer's disease : JAD 2004
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Human Monoclonal Progesterone Receptor Primary Antibody for IP, WB - ABIN1042662
Weigel, Beck, Estes, Prendergast, Altmann, Christensen, Edwards: Ligands induce conformational changes in the carboxyl-terminus of progesterone receptors which are detected by a site-directed antipeptide monoclonal antibody. in Molecular endocrinology (Baltimore, Md.) 1992
Mouse (Murine) Monoclonal Progesterone Receptor Primary Antibody for IP, WB - ABIN1042666
Narayanan, Edwards, Weigel: Human progesterone receptor displays cell cycle-dependent changes in transcriptional activity. in Molecular and cellular biology 2005
In progesterone control of myometrial contractility during pregnancy and labour, while liganded nuclear progesterone receptor B can suppress the expression of Cx43 (show GJA1 Antibodies), unliganded progesterone receptor A paradoxically translocates to the nucleus where it acts as a transcriptional activator of this labour gene.
Progesterone receptor, EGFR (show EGFR Antibodies), and galectin-3 (show LGALS3 Antibodies) are expressed differentially in uterine smooth muscle tumors.
Estrogen receptor (ER (show ESR1 Antibodies)) and progesterone receptor (PR) expression in endometrial carcinoma (EC) were significantly higher than those in the paracarcinoma tissue and control.
TIMP-3 (show TIMP3 Antibodies) mRNA expression levels positively correlates with levels of miR (show MLXIP Antibodies)-21 in in situ breast carcinomas and negatively in progesterone receptor positive invasive breast carcinomas.
results suggest differential downstream progesterone receptor signalling, as progesterone receptor regulates MMP3 (show MMP3 Antibodies)/10 expression via HIF1A (show HIF1A Antibodies), which is not involved in ADAMTS-1 (show ADAMTS1 Antibodies) expression
Association of progesterone receptor gene polymorphism with threatened abortion.
Villin, Pro-Ex-C and progesterone/estrogen receptor (show ESR1 Antibodies) expression have diagnostic and predictive roles in endocervical and endometrioid adenocarcinoma.
In ovarian serous carcinoma, NF-kappaB (show NFKB1 Antibodies) nuclear expression correlated with the 4th edition WHO grade and PR was a favorable prognostic factor for ovarian serous carcinoma.
Patients with Estrogen- and progesterone receptors-positive invasive lobular carcinoma (ILC (show CCL27 Antibodies)) and invasive ductal carcinoma (IDC (show LMNA Antibodies))have similar quantitative ER and PR expression profiles, implicating that ER/PR expression is unlikely to be a confounding factor in studies concerning chemo-sensitivity of ILC (show CCL27 Antibodies) and IDC (show LMNA Antibodies)
The progesterone receptor B (PRB (show RB1 Antibodies)) and androgen Receptor (AR (show AR Antibodies)) mRNA levels were highest in tumors.
Our results identified PIK3IP1 (show PIK3IP1 Antibodies) as a novel target of ARID1A (show ARID1A Antibodies) and PGR in the murine uterus.
Glandular epithelial androgen receptor (AR (show AR Antibodies)) inactivation (with persistent stromal AR action) enhanced PTEN deletion-induced uterine pathology possibly by downregulating progesterone receptor expression in the uterus.
Studies indicate that progesterone receptor transgenic (Pgrcre/+) mitogen inducible gene 6 (Mig-6over) phosphatase and tensin homolog protein (Ptenf/f) knockout mice exhibited an increase of phospho-ERK1/2 and its target genes.
loss of PGR impairs kisspeptin secretory machinery and therefore that PGR plays a critical role in regulating kisspeptin secretion.
PR isoforms are differentially regulated by estradiol and that the induction of PR-B expression is associated to specific transcription factors interactions and epigenetic changes in its promoter in embryonic hypothalamic cells.
The results show that mPges-1 (show PTGES Antibodies) may be a direct downstream target gene of the progesterone receptor.
Progesterone receptor antagonism inhibits progestogen-related carcinogenesis and suppresses tumor cell proliferation.
generated a model to study the consequence of increased Notch (show NOTCH1 Antibodies) signaling in female reproduction and provide the first evidence, to our knowledge, that Notch (show NOTCH1 Antibodies) signaling can regulate epigenetic modification of the progesterone receptor
Calvarial cells had more potential to differentiate into osteoblasts and displayed more osteogeic markers after the PR expression was ablated from the Mx1+ cells. This indicates that PRs may play a role in the later stages of osteoblast differentiation.
progesterone receptor is a key contributor to the hypoxic ventilatory response in newborn mice
Data suggest that the classical xPR-1, located at the plasma membrane, mediates reinitiation of the meiotic cell cycle in the X. laevis oocyte through a non-genomic mechanism.
Xenopus laevis progesterone receptor is capable of associating with the plasma membrane and this association is through its ligang-binding domain.
The expression of progesterone receptor in the uterotubular junction after deep intrauterine insemination with a reduced number of sperm was lower than after conventional artificial insemination and might influence sperm transportation and fertilization.
the digitonin-soluble progesterone binding protein (show PGRMC1 Antibodies) has a binding site that differs from that of membrane PR; it is concluded that more than one progesterone receptor is present in porcine spermatozoa.
The expression of mRNAs for ERalpha (show ESR1 Antibodies), ERbeta (show ESR2 Antibodies) and PR in the sow uterus differed between endometrium and myometrium as well as with stages of the estrous cycle and early pregnancy.
Pgr is widely distributed in all regions of the zebrafish brain.
The localization of Pgr suggests that it mediates progestin regulation of reproductive signaling in the brain, early germ cell proliferation in testis, and ovarian follicular functions, but not final oocyte or sperm maturation.
11 beta-hydroxysteroid dehydrogenase activity stimulated by DHP (show DPYS Antibodies) via Pgr
In vitro and in vivo effects of PGR knockdown in Luteinized granulosa cells also support the hypothesis that Progesterone enhances its own synthesis in the primate corpus luteum by promoting luteinization.
Data suggest that there are no changes in expression or localization patterns for PGR and PGRMC1 (show PGRMC1 Antibodies) (progesterone receptor membrane component 2 (show PGRMC2 Antibodies)) in endometrium in artificially cycled disease-free animals compared with an endometriosis model.
expression differences among PGR genotypes in oviduct and uterus and when differences appear during gestation
During early pregnancy mares had the same pattern of progesterone receptor in the endometrium as that reported for other mammals; namely, a loss of progesterone receptor from the endometrial epithelia but continued localization in stromal cells.
A differential timing of expression of Pgr and Cebpb (show CEBPB Antibodies) in the preovulatory follicles appears to explain the considerably long time-lag (show STMN1 Antibodies) from the pgr gene activation to mmp15 (show MMP15 Antibodies) gene expression.
These results indicate that ptger4b expression is regulated by a genomic mechanism involving Pgr.
Progesterone upregulation of Gs proteins increases VIP (show Vip Antibodies)-induced inhibition of intestinal smooth muscle cell contraction mediated by progesterone receptor A.(progesterone receptor A)
This gene encodes a member of the steroid receptor superfamily. The encoded protein mediates the physiological effects of progesterone, which plays a central role in reproductive events associated with the establishment and maintenance of pregnancy. This gene uses two distinct promotors and translation start sites in the first exon to produce two isoforms, A and B. The two isoforms are identical except for the additional 165 amino acids found in the N-terminus of isoform B and mediate their own response genes and physiologic effects with little overlap.
nuclear receptor subfamily 3 group C member 3
, p4 receptor
, Nuclear receptor subfamily 3 group C member 3
, progesterone receptor
, nuclear progesterone receptor Pgr