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anti-Human Growth Hormone 1 Antibodies:
anti-Mouse (Murine) Growth Hormone 1 Antibodies:
anti-Rat (Rattus) Growth Hormone 1 Antibodies:
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Human Monoclonal Growth Hormone 1 Primary Antibody for ICC, IF - ABIN268996
Thompson, Seethala, Müller: Ectopic sphenoid sinus pituitary adenoma (ESSPA) with normal anterior pituitary gland: a clinicopathologic and immunophenotypic study of 32 cases with a comprehensive review of the english literature. in Head and neck pathology 2012
Rat (Rattus) Polyclonal Growth Hormone 1 Primary Antibody for IHC (fro), WB - ABIN2473905
Ailus, Melamies, Tuomi, Palosuo, Aho: IgM-rheumatoid factors measured by ELISA in non-rheumatoid sera: comparison of human and rabbit Fc fragments as antigens. in British journal of rheumatology 1992
Show all 2 Pubmed References
Human Polyclonal Growth Hormone 1 Primary Antibody for - ABIN285499
Staloch, Divine, Witten, Simon: C/EBP and Cdx family factors regulate liver fatty acid binding protein transgene expression in the small intestinal epithelium. in Biochimica et biophysica acta 2005
Human Monoclonal Growth Hormone 1 Primary Antibody for FACS, IF - ABIN5578783
Niall, Hogan, Sauer, Rosenblum, Greenwood: Sequences of pituitary and placental lactogenic and growth hormones: evolution from a primordial peptide by gene reduplication. in Proceedings of the National Academy of Sciences of the United States of America 1971
The intrinsic amyloidogenicity of growth hormone, in the presence of contaminating prion protein (show PRNP Antibodies) (and perhaps prolactin (show PRL Antibodies) as well) and amyloid-beta contained in some cadavers' pituitaries, may have led to the observed co-occurring of Creutzfeldt-Jakob disease and Alzheimer's disease.
To our knowledge, c.-223C>T is the first homozygous point mutation in the GH1 promoter that leads to short stature due to idiopathic growth hormone deficiency.
Data show that the recombinant protein produced by the plasmid-free E coli strain was purified and characterized to be human growth hormone (hGH).
Our results suggest that the known protective effect of GH signaling deficiency on neoplastic tissue growth is mediated, at least partially, by regulating p53 (show TP53 Antibodies) expression
Gene polymorphism of leptin (loci rs7799039) and leptin receptor (loci rs1137101) are correlated with Growth hormone deficiency susceptibility.
These results showed that hybrid training system on a cycle ergometer (CE) was more efficient in stimulating acute increases in GH, lactate and IL-6 (show IL6 Antibodies) than CE at the same workload.
Growth Hormone 1 T1663A Polymorphism were at a decreased risk of breast cancer.
GH and IGF-1 (show IGF1 Antibodies) suppression is maintained for up to 25 months during pasireotide LAR (show PTPRF Antibodies) treatment of acromegaly.
Effect of oral glucose administration on rebound growth hormone release in normal and obese women: the role of adiposity, insulin (show INS Antibodies) sensitivity and ghrelin (show GHRL Antibodies).
the phenotype of MIP (show TNPO1 Antibodies)-FoxM1 (show FOXM1 Antibodies)-hGH mice is due primarily to hGH activity and that the FoxM1 (show FOXM1 Antibodies) protein remains largely inactive
These results indicate that up-regulation of GH in the lungs of DJ-1 (show PARK7 Antibodies) KO mice may enhance the malignancy of B16F10 cells and nodule formation in pulmonary metastasis of melanoma.
Confirmation of the impairment of GH-IGF-1 (show IGF1 Antibodies) release in hyperphagic MC4R (show MC4R Antibodies) KO mice suggests a role for insulin (show INS Antibodies) in regulating both the release of GH, but also in mediating growth during periods of physiologically suppressed GH-IGF-1 (show IGF1 Antibodies) levels
When charged with hypoxia-ischemia, mutant brains with deleted IGF-1 (show IGF1 Antibodies) receptor were broadly protected from cell damage, neuroinflammation and cerebral edema.
Thiol-disulfide exchange reactions in hGH and related model peptides were influenced by higher order structure, by the size of the thiol reactant and by an Arg residue adjacent to Cys (show DNAJC5 Antibodies) in the thiol reactant.
Growth hormone deficient mice exhibited renal hypertrophy in tubular epithelial cells.
observations demonstrate that germline loss of ghrelin-O-acyltransferase alters Growth Hormone release and patterning
alter miR (show MLXIP Antibodies)-19b concentrations in hematopoietic stem cells (HSCs) and affect HSC (show FUT1 Antibodies) migration
Moderate elevations in circulating GH and IGF-I (show IGF1 Antibodies) can directly increase basal insulin (show INS Antibodies) secretion without impacting beta-cell mass, independent of changes in whole body insulin (show INS Antibodies) sensitivity and hyperlipidemia.
Acylated ghrelin (show GHRL Antibodies) is not required for the surge in pituitary growth hormone observed in pregnant mice.
STAT5 (show STAT5A Antibodies) signaling is increased in the liver in GH-transgenic mice during the growth period, with a balance between positive and negative effectors resulting in accelerated but controlled growth.
An SNP GH4.1 in a growth hormone gene was significantly related to a weaning weight.
The association of IGF1 (show IGF1 Antibodies), GH, and PIT1 (show POU1F1 Antibodies) markers with growth and reproductive traits were assessed.
The total frequencies for the combined genotypes for the bGH and RORC (show RORC Antibodies) genes, which provide for superior meat quality and carcass weight, in the populations of Kazakh white-headed cattle
Whereas only moderate structural changes were observed with up-regulation of GH/IGF-I (show IGF1 Antibodies) axis, disruption of the GH receptor (show GHR Antibodies) had pronounced effects upon tendon ultra-structure.
this study identifies a biochemical mechanism for the regulation of SCFAs on bovine GH and PRL (show PRL Antibodies) gene transcription in dairy cow anterior pituitary cells
homozygote genotypes of GH (LL) and beta-LG (AA) were superior compared to heterozygote genotypes, whereas, the heterozygote genotype of Pit-1 (show POU1F1 Antibodies) gene (AB) was desirable
one GH1 SNP, GH33, was significantly associated with milk protein (show CSN2 Antibodies) yield in the second lactation. Several GH1 SNPs were significantly associated with fertility.
GH and IGF-I (show IGF1 Antibodies) genotypes had no substantial effect on productive parameters, though IGF-I (show IGF1 Antibodies) genotype affected calving-first service interval in primiparous cows. However, the genotypes do alter the endocrine/metabolic profiles of the transition dairy cow.
Association of cattle growth hormone gene polymorphism with milk productivity
Leptin modulation of lymphocytic growth hormone plays a role in the regulation of immune response during pregnancy.
Data indicate that the dual effects of cortistatin (show CORT Antibodies) on growth hormone release parallel those of somatostatin (show SST Antibodies) and are probably mediated by the same receptor(s) and signaling pathway(s) for both peptides.
ghrelin increased growth hormone secretion but not growth hormone synthesis by ovarian follicles
Plasma levels of growth hormone (as well as glucose, insulin (show INS Antibodies), and leptin (show LEP Antibodies)) are highly correlated with the duration of winter anovulatory phase.
Expression of PRL (show PRL Antibodies) and GH in the guinea pig is prominent in the anterior pituitary, similar to known expression patterns of PRL (show PRL Antibodies) and GH for other species.
that concomitant overexpression of GH and GHR (show GHR Antibodies) resulted in a strong decrease of the somatotrophic axis intracellular signaling by diminishing its principal transcription factor signal transducer and activator of transcription 5.1 (show STAT5B Antibodies).
Effects of somatotrophic axis (GH/GHR (show GHR Antibodies)) double transgenesis on structural and molecular aspects of the zebrafish immune system
The zebrafish gh1 mutant, vizzini, exhibits decreased somatic growth, increased adipose tissue accumulation, and disrupted adipose plasticity after nutrient deprivation.
tbx5 (show TBX5 Antibodies) knockdown causes a pseudo GH deficiency in zebrafish during early embryonic stages, and supplementation of exogenous GH can partially restore dysmorphogenesis, apoptosis, cell growth inhibition, and abnormal cardiomyogenesis
Findings show similar regulatory growth hormone (GH) and insulin-like growth factor 1 (IGF-1 (show IGF1 Antibodies)) responses in both Atlantic salmon and rainbow trout.
The protein encoded by this gene is a member of the somatotropin/prolactin family of hormones which play an important role in growth control. The gene, along with four other related genes, is located at the growth hormone locus on chromosome 17 where they are interspersed in the same transcriptional orientation\; an arrangement which is thought to have evolved by a series of gene duplications. The five genes share a remarkably high degree of sequence identity. Alternative splicing generates additional isoforms of each of the five growth hormones, leading to further diversity and potential for specialization. This particular family member is expressed in the pituitary but not in placental tissue as is the case for the other four genes in the growth hormone locus. Mutations in or deletions of the gene lead to growth hormone deficiency and short stature.
pituitary growth hormone
, growth hormone 12
, growth hormone
, growth hormone 1
, neural retina growth hormone
, gnRH receptor
, gonadotropin-releasing hormone receptor
, chorionic somatommamotropin hormone 4
, Pituitary growth hormone
, growth hormone I
, Growth hormone