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Human AMH ELISA Kit for Competition ELISA - ABIN414951
Lin, Wang, Weng, Sheng, Jiang, Yang et al.: Influence of gonadotropin-releasing hormone agonist on the effect of chemotherapy upon ovarian cancer and the prevention of chemotherapy-induced ovarian damage: an experimental study with nu/nu ... in Journal of Zhejiang University. Science. B 2012
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Rat (Rattus) AMH ELISA Kit for Competition ELISA - ABIN1873297
Erba?, Akman, Yava?o?lu, Terek, Akman, Taskiran: Oxytocin improves follicular reserve in a cisplatin-induced gonadotoxicity model in rats. in BioMed research international 2014
Show all 7 Pubmed References
Human AMH ELISA Kit for Competition ELISA - ABIN364999
Ozler, Turgut, Soydinç, Sak, Evsen, Alabalik, Basarali, Deveci: The biochemical and histologic effects of adnexal torsion and early surgical intervention to unwind detorsion on ovarian reserve: an experimental study. in Reproductive sciences (Thousand Oaks, Calif.) 2013
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Rat (Rattus) AMH ELISA Kit for Competition ELISA - ABIN367547
Aiken, Tarry-Adkins, Ozanne: Suboptimal nutrition in utero causes DNA damage and accelerated aging of the female reproductive tract. in FASEB journal : official publication of the Federation of American Societies for Experimental Biology 2013
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Cow (Bovine) AMH ELISA Kit for Sandwich ELISA - ABIN413999
Nfon, Marszal, Zhang, Weingartl: Innate immune response to Rift Valley fever virus in goats. in PLoS neglected tropical diseases 2012
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Mouse (Murine) AMH ELISA Kit for Competition ELISA - ABIN415733
Wang, Qu, Dong, Huang, Kumar, Ji, Wang, Yao, Yang, Wu, Zhang: Long-term effects of methamphetamine exposure in adolescent mice on the future ovarian reserve in adulthood. in Toxicology letters 2016
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Cow (Bovine) AMH ELISA Kit for Competition ELISA - ABIN1873294
Rajak, Kumaresan, Attupuram, Chhillar, Baithalu, Nayak, Sreela, Singh, Tripathi, Mohanty, Yadav: Age-related changes in transcriptional abundance and circulating levels of anti-Mullerian hormone and Sertoli cell count in crossbred and Zebu bovine males. in Theriogenology 2017
Mouse (Murine) AMH ELISA Kit for Competition ELISA - ABIN457143
Lee, Kim, Kong, Youm, Lee, Suh, Kim: A combination of simvastatin and methylprednisolone improves the quality of vitrified-warmed ovarian tissue after auto-transplantation. in Human reproduction (Oxford, England) 2015
Human AMH ELISA Kit for Sandwich ELISA - ABIN455921
Carranza-Lira, Bustamante-Mendoza, Leaños-Miranda, Campos-Galicia, Estrada-Moscoso, Chan-Verdugo, Ramos-Godínez, Moncada-Claudio, Peña-Torres: [Anti-Müllerian hormone serum levels in women with and without uterine fibroids]. in Ginecología y obstetricia de México 2014
Rat (Rattus) AMH ELISA Kit for Sandwich ELISA - ABIN579483
Benian, Guralp, Uzun, Okyar, Sahmay: The effect of repeated administration of methotrexate (MTX) on rat ovary: measurement of serum antimullerian hormone (AMH) levels. in Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology 2013
nuclear receptor subfamily 5, group A, member 1b is a new candidate for sex determination and differentiation in a way similar to steroidogenic factor 1 (show NR5A1 ELISA Kits), possibly involving AMH
zebrafish Anti-Mullerian hormone (Amh) is regulated by sox9a, sox9b, and cyp19a1a during gonad development
amh is a candidate gene down-regulating cyp19a1a, leading to "juvenile ovary-to-testis" transformation.
It was shown that the male-to-female sex reversal phenotype in hotei medaka mutants is not a direct consequence of anti-Mullerian hormone signaling in supporting cells, but is instead mediated by germ cells.
Study found 24 rare AMH variants in patients with PCOS and control subjects; 18 variants were specific to women with PCOS. Seventeen of 18 (94%) PCOS-specific variants had significantly reduced AMH signaling, whereas none of 6 variants observed in control subjects showed significant defects in signaling.
In the obese polycystic ovary syndrome group, anti-mullerian hormone was associated with ghrelin (show GHRL ELISA Kits) levels independent of age, insulin (show INS ELISA Kits), and total testosterone. There was no association between total ghrelin (show GHRL ELISA Kits) and anti-mullerian hormone levels in non-obese women with polycystic ovary syndrome, non-obese controls, or obese controls.
Data suggest that young men and young women initially have similar levels of circulating levels of AMH, but women lose their AMH in parallel with the decrease in their ovarian reserve. Circulating AMH in men is negatively associated with all-cause mortality; men with higher levels of AMH may outlive men with lower levels of AMH. [EDITORIAL]
In young women with polycystic ovary syndrome, low AMH levels predict a greater risk of metabolic syndrome.
MIS/AMH inhibits ovarian cancer by deregulating the Wnt (show WNT2 ELISA Kits) signal pathway via the beta-catenin interacting protein (ICAT (show CTNNBIP1 ELISA Kits)). MIS/AMH upregulated ICAT (show CTNNBIP1 ELISA Kits) in ovarian cancer cell line which caused decreased cell viability, cell cycle arrest and apoptosis.
The AMH level peaked at or before ovulation in most women, trended down with natural pregnancies, and consistently increased or decreased in women with a viable pregnancy after therapy. Nonviable pregnancies showed erratic AMH patterns.
Before 35 years of age, women with type 1 diabetes have lower AMH levels than women without diabetes.
Suggest that activation of AMH by proteolytic enzymes is largely stable throughout the ovarian cycle. However, there is a subtle but robust decrease in the level of proAMH relative to AMHN,C in the acute postovulatory period.
Age is correlated with AMH, but it accounts for only a portion of the variation seen in reproductive age African American women.
AMH was inversely correlated with age in both the fertile and infertile populations and there was no significant difference between the fertile and infertile populations in terms of AMH.
AMH increases GnRH-dependent LH pulsatility and secretion, supporting a central action of AMH on GnRH neurons.
AMH and FOXL2 (show FOXL2 ELISA Kits) collaboratively work to reserve ovarian follicles. AMH is an endogenous target gene of FOXL2 (show FOXL2 ELISA Kits).
Up-regulation of SOX9 (show SOX9 ELISA Kits) in sertoli cells from testiculopathic patients accounts for increasing anti-mullerian hormone expression via impaired androgen receptor (show AR ELISA Kits) signaling.
Male mice require AMH to undergo normal social development.
Data show that Purkinje cells express receptors for Mullerian inhibiting substance (MIS), and that MIS(-/-) male mice have female-like numbers of Purkinje cells and a female-like size to other parts of their cerebellum.
MIS may be involved in anterograde rather than autocrine or retrograde regulation of neurons.
FSH (show BRD2 ELISA Kits) and cAMP stimulate AMH transcription by granulosa cells. FSH (show BRD2 ELISA Kits) and LH have an additive effect, which may be important in polycystic ovary syndrome.
This suggests that MIS is one of the determinants of "boy"-specific behavior.
Role of anti-Mullerian hormone (AMH) as a regulator and marker of ovarian function.
Administration of MIS to male mice induced IEX-1S mRNA in the prostate in vivo, suggesting that MIS may function as an endogenous hormonal regulator of NF-kappaB (show NFKB1 ELISA Kits) signaling and growth in the prostate gland.
This study showed that antral follicle counts (AFC) and AMH levels were repeatable when determined at an unknown stage of follicular growth and expected day of follicular wave emergence, but repeatability was greater for AMH than AFC.
The effects of castration and other surgical intervention on the blood levels of anti-Muellerian hormone, inhibin A (show INHA ELISA Kits), gonadotropins, and gonadotropin receptors in bull calves are reported.
Results from these studies indicate that AMH signaling plays a role in both regulating granulosa cell proliferation and preventing granulosa cells from 5- to 8-mm follicles from undergoing premature differentiation before follicle selection.
These findings indicate the followings: AMH mRNA levels decrease in both dominant and secondary follicles during follicular deviation; granulosa cells from heathy follicles express more AMH mRNA compared to subordinate follicles undergoing atresia and FSH (show BRD2 ELISA Kits) stimulates AMH and AMHR2 (show AMHR2 ELISA Kits) mRNA expression in granulosa cells of co-dominant follicles.
Measurement of AMH concentration in the plasma of cows can help to predict their capacity for embryo production in response to gonadotrophin treatment.
In first study to investigate the blood profile and immunohuistochemistry of anti-Mullerian hormone in bovine granulosa-theca cell tumors, the findings indicated that anti-Mullerian hormone is a novel biomarker for granulosa-theca cell tumors in cattle.
Regulation of anti-Mullerian hormone production in the cow.
Intrafollicular AMH was not a marker of cystic development in the cow, but low AMH concentrations in cysts were associated with luteinization.
AMH expression is modulated by androgens in bovine granulosa cells from small follicles.
Anti-Mullerian hormone is a member of the transforming growth factor-beta gene family which mediates male sexual differentiation. Anti-Mullerian hormone causes the regression of Mullerian ducts which would otherwise differentiate into the uterus and fallopian tubes. Some mutations in the anti-Mullerian hormone result in persistent Mullerian duct syndrome.
, anti-Mullerian hormone
, anti-mullerian hormone
, Mullerian inhibiting factor
, Mullerian inhibiting substance
, anti-Muellerian hormone
, muellerian-inhibiting substance
, Mullerian inhibitory substance
, Anti - Mullerian hormone (Mulerian inhibiting substance)