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anti-Human Growth Hormone Receptor Antikörper:
anti-Mouse (Murine) Growth Hormone Receptor Antikörper:
anti-Rat (Rattus) Growth Hormone Receptor Antikörper:
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Human Polyclonal Growth Hormone Receptor Primary Antibody für IF (p), IHC (p) - ABIN671481
Wang, Zhou, Lin, Wang, Lin, Li: RhGH attenuates ischemia injury of intrahepatic bile ducts relating to liver transplantation. in The Journal of surgical research 2011
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Human Polyclonal Growth Hormone Receptor Primary Antibody für CyTOF, FACS - ABIN4900013
Zhang, Hatano, Shaw, Olde Nordkamp, Jiang, Li, Kollnberger: The Leukocyte Immunoglobulin-Like Receptor Family Member LILRB5 Binds to HLA-Class I Heavy Chains. in PLoS ONE 2015
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Human Polyclonal Growth Hormone Receptor Primary Antibody für IHC (p), IHC - ABIN441424
Xekouki, Pacak, Almeida, Wassif, Rustin, Nesterova, de la Luz Sierra, Matro, Ball, Azevedo, Horvath, Lyssikatos, Quezado, Patronas, Ferrando, Pasini, Lytras, Tolis, Stratakis: Succinate dehydrogenase (SDH) D subunit (SDHD) inactivation in a growth-hormone-producing pituitary tumor: a new association for SDH? in The Journal of clinical endocrinology and metabolism 2012
These results implicate TIMP3 (zeige TIMP3 Antikörper) as a modulator of cell surface GHR abundance and the ability of GH to promote cellular signaling.
GHR and PRLR (zeige PRLR Antikörper) associate in complexes comprised of GHR-GHR/PRLR-PRLR (zeige PRLR Antikörper) heteromers consisting of GHR homodimers and PRLR (zeige PRLR Antikörper) homodimers, rather than GHR-PRLR (zeige PRLR Antikörper) heterodimers.
d3/d3 GHR genotype was found twice as frequent in appropriate for gestational age (AGA (zeige AGA Antikörper)) and large for gestational age (LGA (zeige GLS2 Antikörper)) cohorts compared to small for gestational age (SGA) subjects, whereas no significant differences in the frequency distribution of the GHR genotypes between LGA (zeige GLS2 Antikörper) and AGA (zeige AGA Antikörper) newborns were detected.
Molecular interactions of EphA4 (zeige EPHA4 Antikörper), growth hormone receptor, Jak2 (zeige JAK2 Antikörper), and STAT5B (zeige STAT5B Antikörper) have been described.
GHR levels correlate with levels of lipases and lipid droplet-associated proteins crucial for lipolysis. Thus, higher GHR expression in the abdominal depot when compared with the gluteal depot may underlie the in vivo effect of GH to specifically reduce abdominal adipose tissue mass.
There was a strong relationship between growth hormone receptor (GHR)-d3/fl gene polymorphism status and leptin (zeige LEP Antikörper) levels in acromegalic patients
GHR exon 3 genotype appears to have no clinical significance, at least in Brazilian acromegaly patients.
No differences were observed in GHR genotype distribution between the idiopathic growth hormone (zeige GH1 Antikörper) deficiency (IGHD)patients and the control group. Patients with IGHD did not differ among each other depending on their genotype (fl/fl (zeige FLT3LG Antikörper)-GHR or fl/d3-GHR) in terms of growth velocity before introducing therapy or growth rate after one year of recombinant human GH therapy.
GHR-exon 3 polymorphisms did not show any consistent association with clinical and laboratory features of acromegalic patients even after treatment.
We report a rapid, optimized method for genotyping the GHR full-length versus exon 3-deleted isoform (GHRd3)
A role for GH in influencing hormone signaling in adipose tissue in a depot-dependent manner in GHR-/- knock-out mice.
disruption of cardiomyocyte GH-induced signaling in adult GhrKO mice does not affect cardiac function, but it does play a role in systemic glucose homeostasis, in part through modulation of circulating IGF-1 (zeige IGF1 Antikörper).
Snell, GHKRO, and PAPPA (zeige PAPPA Antikörper)-KO mice express high levels of two proteins involved in DNA repair, O-6-methylguanine-DNA methyltransferase (MGMT (zeige MGMT Antikörper)) and N-myc downstream-regulated gene 1 (NDRG1 (zeige NDRG1 Antikörper)).
adult-onset growth hormone receptor knockout mice (aGHRKO mice), like GHRKO animals, displayed retarded growth and high adiposity with improved insulin (zeige INS Antikörper) sensitivity. Importantly, female aGHRKO animals showed an increase in their maximal lifespan, whereas the lifespan of male aGHRKO mice was not different from controls.
Similar to other mice with decreased GH action, female GHA mice display reduced age-related lipid redistribution and improved insulin (zeige INS Antikörper) sensitivity, but no change in cellular senescence.
The dwarf phenotype was partially corrected via plasmid containing the growth hormone gene administrated intramuscularly, depending on age at treatment.
GHR-dependent downregulation of NLRP3 (zeige NLRP3 Antikörper) inflammasome in macrophages is linked to pro-longevity effects that maintain immune system homeostasis in aging.
both brown adipose tissue (BAT (zeige BAAT Antikörper)) and white adipose tissue (WAT) contribute in different ways to phenotypes in GHRKO mice, with Ghr ablation blunting inflammation in BAT (zeige BAAT Antikörper) as well as cellular metabolism and mitochondrial biogenesis in WAT
Data (including data from studies in knockout mice) suggest Socs2 (suppressor of cytokine signaling 2 (zeige SOCS2 Antikörper)) regulates liver regeneration rate after partial hepatectomy, Ghr level via ubiquitination/proteolysis, and serum Igf1 (insulin-like growth factor-1 (zeige IGF1 Antikörper)).
It was concluded that endogenously secreted PTH (zeige PTH Antikörper) and GHR signaling in bone are necessary to establish radial bone growth and optimize mineral acquisition during growth.
There was no association between the genotypes of GH and IGF-IS and fertility of Holstein cows raised in semiextensive or intensive regimes, while the STAT5 (zeige STAT5A Antikörper) ABstEII polymorphism was associated with calving-first heat interval in Holstein cows raised in the intensive system.
hepatic growth hormone receptor and suppressor of cytokine signaling (SOCS (zeige CISH Antikörper))2 (zeige SOCS2 Antikörper) messenger RNA expression appeared to be promptly and sensitively regulated by increased estradiol levels before ovulation of dairy heifers
Comparatively studied genetic diversity of growth hormone receptor (GHR) in Tibetan cattle and Chinese Holstein cow.
This work confirms the importance of CAPN1 (zeige CAPNL1 Antikörper) and CAST for tenderness in beef, provides a new effect of CAST on beef tenderness, and questions the utility of GHR as a selection marker for beef quality.
the data support the high potential of the growth hormone receptor F279Y polymorphism as a marker for the improvement of milk traits in selection programs
6 of the published GHR SNPs and 7 of the novel GHR SNPs were associated with at least 1 of the traits--milk yield, fat yield, protein yield, fat percentage, protein percentage, somatic cell score, calving interval, survival and growth and size traits.
Effects of GHR p.Phe279Tyr mutations on milk, fat and protein yield, as well as fat and protein percentage in the milk of 1222 Holstein cows was found to be significantly associated with protein percentage.
Food deprivation-induced decrease in circulating IGF-I (zeige IGF1 Antikörper) in steers is associated with decrease in expression of different IGF-I (zeige IGF1 Antikörper) mRNA variants and specific decrease in expression of growth hormone receptor mRNA variants 1C3 and 1A in liver.
Insulin (zeige INS Antikörper) regulates the efficiency of GH signaling in liver and adipose tissue of dairy cows by acting as a rheostat of GHR synthesis.
Results show that chicken ovalbumin upstream promoter transcription factor (zeige NR2F1 Antikörper) II (COUP-TFII (zeige NR2F2 Antikörper)), hepatocyte nuclear factor 4alpha (HNF-4alpha (zeige HNF4A Antikörper)) and HNF-4gamma regulate growth hormone receptor 1A promoter activity by binding to a common DNA element
Castration significantly reduced the serum growth hormone (zeige GH1 Antikörper) and the responses of the growth hormone receptor (GHR)
GHR double-allelic knockout pigs were 50% smaller than that of the controls.
Growth hormone (GH (zeige GH1 Antikörper)) in maturation medium did not increase cumulus expansion in porcine cumulus-oocyte complexes but did improve nuclear maturation, GH had no effect on porcine fertilization and embryo development.
subunit alignment is critical for effective signaling in GH receptor activation
Fos-zippered GHR tails and Jak2 (zeige JAK2 Antikörper), both purified from baculovirus-infected insect cells, interacted via box1 with a binding affinity of approximately 40nM.
Jak2 (zeige JAK2 Antikörper) binding to the growth hormone receptor prevents endocytosis in a non-catalytic manner
GHR gene may be a candidate gene responsible for butcher trait in rabbit.
This gene encodes a member of the type I cytokine receptor family, which is a transmembrane receptor for growth hormone. Binding of growth hormone to the receptor leads to receptor dimerization and the activation of an intra- and intercellular signal transduction pathway leading to growth. Mutations in this gene have been associated with Laron syndrome, also known as the growth hormone insensitivity syndrome (GHIS), a disorder characterized by short stature. In humans and rabbits, but not rodents, growth hormone binding protein (GHBP) is generated by proteolytic cleavage of the extracellular ligand-binding domain from the mature growth hormone receptor protein. Multiple alternatively spliced transcript variants have been found for this gene.
, growth hormone binding protein
, serum binding protein
, somatotropin receptor
, Growth hormone receptor precursor (GH receptor) (GH binding protein) (GHBP) (Serum binding protein)
, growth hormone receptor/binding protein
, growth hormone receptor precursor splice variant D56
, growth hormone receptor variant d5-6
, growth hormone receptor
, growth hormone-binding protein
, serum-binding protein
, Somatotropin receptor