anti-Leptin (LEP) 抗体产品概述

Full name:
anti-Leptin 抗体 (LEP)
在www.antibodies-online.cn可供594 Leptin (LEP) 抗体的34不同的供货商。 再加上,我们可以发Leptin 蛋白 (199)Leptin 试剂盒 (192)和数多这个蛋白质的别的产品。 总共1022 Leptin产品已列进来了。
别名:
LEPD, OB, obese, OBS

所有可销售的anti-Leptin 抗体

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引用最多的anti-Leptin 抗体

  1. Mouse (Murine) Polyclonal Leptin Primary Antibody for EIA, WB - ABIN115496 : Maffei, Halaas, Ravussin, Pratley, Lee, Zhang, Fei, Kim, Lallone, Ranganathan: Leptin levels in human and rodent: measurement of plasma leptin and ob RNA in obese and weight-reduced subjects. in Nature medicine 1995 (PubMed)
    Show all 6 references for 115496

  2. Human Monoclonal Leptin Primary Antibody for EIA, WB - ABIN114695 : Lönnqvist, Arner, Nordfors, Schalling: Overexpression of the obese (ob) gene in adipose tissue of human obese subjects. in Nature medicine 1995 (PubMed)
    Show all 6 references for 114695

  3. Human Polyclonal Leptin Primary Antibody for EIA, IF - ABIN358628 : Tank, Jordan, Diedrich, Schroeder, Furlan, Sharma, Luft, Brabant: Bound leptin and sympathetic outflow in nonobese men. in The Journal of clinical endocrinology and metabolism 2003 (PubMed)
    Show all 4 references for 358628

  4. Human Polyclonal Leptin Primary Antibody for EIA, FACS - ABIN953161 : Friedlander, Li, Fornage, Williams, Lewis, Schreiner, Pletcher, Enquobahrie, Williams, Siscovick: Candidate molecular pathway genes related to appetite regulatory neural network, adipocyte homeostasis and obesity: results from the CARDIA Study. in Annals of human genetics 2010 (PubMed)
    Show all 2 references for 953161

  5. Human Monoclonal Leptin Primary Antibody for ELISA, IF - ABIN1996123 : Sun, Park, Gupta, Holland, Auerbach, Zhang, Goncalves Marangoni, Nicoloro, Czech, Varga, Ploug, An, Scherer: Endotrophin triggers adipose tissue fibrosis and metabolic dysfunction. in Nature communications 2014 (PubMed)

  6. Human Polyclonal Leptin Primary Antibody for EIA - ABIN318591 : Mantzoros: The role of leptin in human obesity and disease: a review of current evidence. in Annals of internal medicine 1999 (PubMed)

更多抗Leptin的相互作用对抗体

Mouse (Murine) Leptin (LEP) interaction partners

  1. High fat diet attenuates leptin signaling throughout the brain, but some brain regions maintain their ability to sense leptin. Weight loss restores leptin sensing to some degree in most (but not all) brain regions, while other brain regions display hypersensitivity to leptin following weight loss

  2. CNS-specific Tak1 (显示 NR2C2 抗体) deletion prevented ER-stress-induced hypothalamic leptin resistance and hyperphagic obesity under a high-fat diet (HFD). Thus, TAK1 (显示 NR2C2 抗体) is a crucial regulator of ER stress in vivo, which could be a target for alleviation of ER stress and its associated disease conditions.

  3. These data further implicate IL-6 (显示 IL6 抗体) in fatty liver disease modulation in the context of DIO, and indicate that continuous stimulation with IL-6 (显示 IL6 抗体) attenuates the IL-6 (显示 IL6 抗体)-receptor response, which is associated with high serum levels of leptin.

  4. these data unmasked a role for mitochondrial fission in leptin sensitivity and glucose sensing of POMC (显示 POMC 抗体) neurons.

  5. Obesity and leptin deficiency substantially decreased morphine metabolism and clearance.

  6. These findings suggest that by impairing the testicular LEP-JAK (显示 JAK3 抗体)-STAT (显示 STAT1 抗体) pathway, early-stage obesity inhibits the biosynthesis of testosterone and sexual development and reduces male reproductive potential. Long-term moderate and high-volume exercise can effectively reduce body fat and improve obesity-induced abnormalities in testicular leptin signal transduction, whereas only moderate-volume exercise can reverse the negativ

  7. genetic and pharmacological ablation of adult NG2 (显示 Vcan 抗体)-glia (also known as oligodendrocyte precursors), but not microglia, leads to primary leptin resistance and obesity in mice.

  8. a novel mechanism of leptin-induced fatty acid oxidation in muscle tissue; namely, this process is dependent on the activation of AMPK (显示 PRKAA1 抗体) to induce the translocation of FAT/CD36 (显示 CD36 抗体) to the plasma membrane, thereby stimulating fatty acid uptake.

  9. Results demonstrate that in white adipose tissue, leptin expression and secretion is promoted by Epac1 (显示 RAPGEF3 抗体), hence regulating energy balance and glucose homeostasis.

  10. may regulate growth hormone (显示 GH1 抗体) expression in somatotropes through the stimulation of POU1F1 (显示 POU1F1 抗体)

Human Leptin (LEP) interaction partners

  1. Leptin, at concentrations with minimal or no activating effects on astrocytoma cells, enhanced growth and migration promoted by low doses of sPLA2-IIA (显示 PLA2G2A 抗体). sPLA2-IIA (显示 PLA2G2A 抗体) alone induced a transient phosphorylation pattern in the Src (显示 SRC 抗体)/ERK (显示 EPHB2 抗体)/Akt (显示 AKT1 抗体)/mTOR (显示 FRAP1 抗体)/p70S6K (显示 RPS6KB1 抗体)/rS6 pathway through EGFR (显示 EGFR 抗体) transactivation

  2. a novel mechanism by which compromised HDLECs maintain their homeostasis during inflammation mediated by leptin and IL-6 (显示 IL6 抗体)

  3. In this study of a predominantly minority population, no association between premorbid leptin levels and cancer incidence was demonstrated

  4. Centenarians had significant higher serum levels of leptin compared with controls (p<0.001), whereas no significant differences were observed for adiponectin (显示 ADIPOQ 抗体).

  5. Studies suggest that metformin treatment was not associated with a decrease in blood leptin levels, or increases in blood ghrelin (显示 GHRL 抗体) levels in patients with type 2 diabetes mellitus (T2DM).

  6. higher prediagnostic levels of plasma leptin were associated with an elevated risk of pancreatic cancer among men, but not among women

  7. Leptin levels are not significantly associated with incident atrial fibrillation in women.

  8. Results found an association between DNA methylation (显示 HELLS 抗体) in each CpG site of the gene LEP, measured in saliva (显示 RAG1AP1 抗体), and obesity-related measures in 431 children aged 10- 15 years old. This association differed by sex and obesity status, with a much stronger association in obese boys.

  9. Data suggest caloric restriction modifies response of ovarian granulosa cells to leptin on cell proliferation/apoptosis, MAP kinase (显示 MAPK1 抗体) signaling, and release of hormones (estradiol and IGFI (显示 IGF1 抗体)). The caloric restriction studies were conducted in rabbits; then, isolated rabbit granulosa cells were exposed to recombinant human leptin. (IGF1 (显示 IGF1 抗体) = insulin-like growth factor I (显示 IGF1 抗体))

  10. Data suggest that modest weight loss in overweight adults due to caloric restriction and exercise decreases serum leptin (LEP) and high molecular weight adiponectin (ADPN), and increases serum pentraxin-3 (PTX3 (显示 PTX3 抗体)) in a manner that correlates with increased insulin (显示 INS 抗体) sensitivity.

Pig (Porcine) Leptin (LEP) interaction partners

  1. The lack of effect of heat stress on the expression of leptin suggests that this peptide may not be involved in the reduction of feed intake of HS acclimated pigs.

  2. A high variability of the LEP was detected in the different analysed populations providing new data for the existence of two domestication centres in Asia.

  3. The presence of leptin and ObR (显示 LEPR 抗体)-b varies across parities and is more intense in the uterus, ovaries and hypothalamus of females that were cycling before culling than in those having cystic ovaries.

  4. Studied 3'UTR (显示 UTS2R 抗体) leptin polymorphism regulatory sequences' affect on gene expression and their association with production traits.

  5. These results suggest that LEPR, MC4R, PIK3C3 and VRTN are useful markers for accurately predicting breeding values in Duroc pigs.

  6. Data showing changes in expression patterns of LEP/LEPR (显示 LEPR 抗体) in endometrium/chorioallantoic membrane during placentation/fetal development suggest role for LEP/LEPR (显示 LEPR 抗体) complex at early stages of pregnancy, possibly affecting the attachment process.

  7. Another funning discovery is ob-Rb (显示 LEPR 抗体) mRNA in porcine endometrium was mainly negative-regulated by leptin

  8. Characterization of a distinctive pattern of periovulatory leptin secretion and its relationship with ovulation rate and luteal function in swine with obesity/leptin resistance

  9. Leptin and leptin receptor (显示 LEPR 抗体) are expressed in porcine luteal cells, and there is a modulatory effect of LH, estradiol (E) and progesterone (P) on leptin mRNA expression as well as E and P on leptin secretion by those cells obtained in early pregnancy.

  10. The present study aimed to determine the effects of breed and sex on growth patterns and metabolic features of advanced-pregnancy foetuses from lean and obese/leptin resistant swine.

Cow (Bovine) Leptin (LEP) interaction partners

  1. Consistent with this, leptin enhanced GnRH (显示 GNRH1 抗体)-induced secretion of LH measured by ELISA. We suggest that leptin enhances membrane expression of voltage-gated Na(+) and Ca(2 (显示 CA2 抗体)+) channels, which results in a modulation of the action potential properties and an increase in hormone release from gonadotropes.

  2. The effects of a single nucleotide polymorphism of leptin on weight gain and body composition are reported.

  3. A leptin SNP (LEPg.978) was significantly associated with a weight at one year.

  4. The results of this study suggest that leptin physiology could be a candidate for mechanisms that contribute to feed intake and feed efficiency variation in beef cattle.

  5. Leptin concentrations could be a useful physiological marker for growth and feed efficiency of finishing beef cattle.

  6. Hormonal gene expression involved in residual feed intake in dairy cows may be related to the molecular regulation of the leptin-NPY (显示 NPY 抗体) and insulin (显示 INS 抗体) signaling pathways.

  7. Leptin R25C genotype impacted most traits associated with fatness.

  8. The absence of A80V polymorphism (C --> T at position 95691973 bp of leptin gene) has been established in the genotypes of Ayrshire cattle as compared to Holstein cattle.

  9. Data indicate that increased body weight gain during juvenile development accelerates sexual maturation in heifers, coincident with reciprocal changes in circulating concentrations of leptin and hypothalamic neuropeptide Y (NPY (显示 NPY 抗体)) release.

  10. SNP LEP significantly affected milk, protein and fat yield (P<0.05), and age at first calving (P<0.01) in analyzed population of cows. SNP LEPR (显示 LEPR 抗体)/T945M affected significantly calving interval (P<0.01) only

Goat Leptin (LEP) interaction partners

  1. polymorphisms of the LEP gene might be important genetic factors influencing growth traits, and these genetic markers may be useful for future marker-assisted selection programs in goat breeding and production

Rabbit Leptin (LEP) interaction partners

  1. study suggests that increased CSF (显示 CSF2 抗体) leptin, likely from blood-brain barrier breakdown, combined with elevated serum GH and IGF-1 (显示 IGF1 抗体) after traumatic brain injury, leads to accelerated fracture healing

  2. We conclude that offspring from mothers consuming a high fat diet exhibit an adverse cardiovascular profile in adulthood because of altered central hypothalamic sensitivity to leptin and ghrelin (显示 GHRL 抗体).

  3. Niacin Reduces serum level and adipose mRNA expression of leptin and up-regulates PPARgamma (显示 PPARG 抗体) and CD36 (显示 CD36 抗体) mRNA expression in hypercholesterolemic rabbits.

Horse (Equine) Leptin (LEP) interaction partners

  1. Positive correlations were found between leptin and total lipids, triglycerides, VLDLs, Total-Chol, and LDLs.

  2. Leptin metabolism in obese ponies following a return to free feeding after a period of food deprivation is reported.

  3. Plasma levels of leptin (as well as glucose, insulin (显示 INS 抗体), and growth hormone (显示 GH1 抗体)) are highly correlated with the duration of winter anovulatory phase.

  4. GHRL (显示 GHRL 抗体), LEP, ADIP (显示 SSX2IP 抗体), INS (显示 INS 抗体) and CORT (显示 CORT 抗体) concentrations were measured using radioimmunoassay

  5. positive correlation between leptin and estradiol led us to suggest that leptin hormone plays an important role in ovulation of the first postpartum estrus in mares

Rhesus Monkey Leptin (LEP) interaction partners

  1. The effects of exogenous human kisspeptin-10 (KP10) were studied on three important adipokines, namely, adiponectin (显示 ADIPOQ 抗体), leptin, and resistin (显示 RETN 抗体) in a set of four chair-restraint habituated intact adult male rhesus monkeys.

  2. results do not support a role for reduced leptin secretion in anovulation induced by dietary restriction

Leptin (LEP) 抗原简介

Antigen Summary

This gene encodes a protein that is secreted by white adipocytes, and which plays a major role in the regulation of body weight. This protein, which acts through the leptin receptor, functions as part of a signaling pathway that can inhibit food intake and/or regulate energy expenditure to maintain constancy of the adipose mass. This protein also has several endocrine functions, and is involved in the regulation of immune and inflammatory responses, hematopoiesis, angiogenesis and wound healing. Mutations in this gene and/or its regulatory regions cause severe obesity, and morbid obesity with hypogonadism. This gene has also been linked to type 2 diabetes mellitus development.

Alternative names and synonyms associated with Leptin (LEP)

  • leptin (Lep) 抗体
  • leptin (LEP) 抗体
  • leptin (lep) 抗体
  • LEPD 抗体
  • OB 抗体
  • obese 抗体
  • OBS 抗体

Protein level used designations for anti-Leptin (LEP) 抗体

obesity factor , leptin (murine obesity homolog) , leptin (obesity homolog, mouse) , obese protein , obese, mouse, homolog of , obese

GENE ID SPECIES
16846 Mus musculus
3952 Homo sapiens
25608 Rattus norvegicus
443534 Ovis aries
396832 Sus scrofa
280836 Bos taurus
100860794 Capra hircus
100008747 Oryctolagus cuniculus
373955 Gallus gallus
403616 Canis lupus familiaris
100034042 Equus caballus
493838 Felis catus
449638 Pan troglodytes
100716751 Cavia porcellus
698728 Macaca mulatta
548631 Takifugu rubripes
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