Leptin Mouse/Rat ELISA

Regulatery Status: RUO
Type: Sandwich ELISA, Biotin-labelled antibody
Other Names Status: Obesity factor, Obese protein, LEP, OB, OBS
Species: Mouse, Rat
Catalog No Size
Product Catalog No: RD291001200R Pack Size: 96 wells (1 kit)

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Product Features

Leptin is a protein hormone with important effects in metabolism and regulating body weight. It is a single-chain 16 kDa protein consisting of 146 amino acid residues and encoded by the obese (ob) gene. Leptin is expressed predominantly by adipocytes, small amounts of leptin are also secreted by cells in the epithelium of stomach and in the placenta. Leptin´s effect on body weight is mediated through effects on hypothalamic centers, where leptin receptors are highly expressed. Leptin has a dual action, it decreases the appetite and increases energy consumption.

A mutations in the ob gene of leptin or in the gene of leptin receptor causes hyperphagia, reduced energy expenditure, and severe obesity in the ob/ob mice. Ob gene knockout mice are also characterized by several metabolic abnormalities including hyperglucocorticoidemia, hyperglycaemia, hyperinsulinemia and insulin resistance. When ob/ob mice are treated with injections of leptin, they lose their excess fat and return to normal body weight. Studies have shown that leptin appears to be a significant regulator of reproductive function. In addition, leptin is involved in bone metabolism and plays a significant role as an immunomodulator.

Features

  • The total assay time is less than four hours.
  • The kit measures total serum leptin.
  • Quality controls are mouse and rat serum based. No human sera are used.

Research topic

Animal studies, Diabetology – Other Relevant Products, Energy metabolism and body weight regulation, Reproduction

Technical Sheet / Info

Type

Sandwich ELISA, Biotin-labelled antibody

Applications

Serum, Plasma-EDTA, Plasma-Heparin, Plasma-Citrate

Sample Requirements

7 µl/well

Storage/Expiration

Store the kit at 2–8°C. Under these conditions, the kit is stable until the expiration date (see label on the box).

Calibration Curve

Calibration Range

100–4000 pg/ml

Limit of Detection

Analytical Limit of Detection is calculated from the real leptin values in wells and is 30 pg/ml for mouse leptin and 50 pg/ml for rat leptin

Intra-assay (Within-Run)

n = 8; CV = 2.2%

Inter-assay (Run-to-Run)

n = 8; CV = 3.4%

Spiking Recovery

94,50%

Dilutation Linearity

96,70%

Crossreactivity

bovine        Non-detectable
cat           Non-detectable
dog           Non-detectable
goat          Non-detectable
hamster       Non-detectable
horse         Non-detectable
monkey        Non-detectable
pig           Non-detectable
rabbit        Non-detectable
sheep         Not tested
chicken       Not tested
mouse         Yes
rat           Yes
human         Yes (recommended dilution 1:3)
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References

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– Bartels ED, Nielsen JM, Hellgren LI, Ploug T, Nielsen LB. Cardiac expression of microsomal triglyceride transfer protein is increased in obesity and serves to attenuate cardiac triglyceride accumulation. PLoS One. 2009;4 (4):e5300

– Bol VV, Delattre AI, Reusens B, Raes M, Remacle C. Forced catch-up growth after fetal protein restriction alters the adipose tissue gene expression program leading to obesity in adult mice. Am J Physiol Regul Integr Comp. 2009 Aug;297 (2):R291-9

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– Gout J, Sarafian D, Tirard J, Blondet A, Vigier M, Rajas F, Mithieux G, Begeot M, Naville D. Leptin infusion and obesity in mouse cause alterations in the hypothalamic melanocortin system. Obesity (Silver Spring). 2008 Aug;16 (8):1763-9

– Kenny S, Gamble J, Lyons S, Vlatkovic N, Dimaline R, Varro A, Dockray GJ. Gastric expression of plasminogen activator inhibitor (PAI)-1 is associated with hyperphagia and obesity in mice. Endocrinology. 2013 Feb;154 (2):718-26

– Kirk SL, Samuelsson AM, Argenton M, Dhonye H, Kalamatianos T, Poston L, Taylor PD, Coen CW. Maternal obesity induced by diet in rats permanently influences central processes regulating food intake in offspring. PLoS One. 2009;4 (6):e5870

– Putakala M, Gujjala S, Nukala S, Desireddy S. Beneficial Effects of Phyllanthus amarus Against High Fructose Diet Induced Insulin Resistance and Hepatic Oxidative Stress in Male Wistar Rats. Appl Biochem Biotechnol. 2017 Mar 28. doi: 10.1007/s12010-017-2461-0

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– Rodriguez L, Panadero MI, Rodrigo S, Roglans N, Otero P, Alvarez-Millan JJ, Laguna JC, Bocos C. Liquid fructose in pregnancy exacerbates fructose-induced dyslipidemia in adult female offspring. J Nutr Biochem. 2016 Jun;32:115-22

– Rohrbach S, Aurich AC, Li L, Niemann B. Age-associated loss in adiponectin-activation by caloric restriction: lack of compensation by enhanced inducibility of adiponectin paralogs CTRP2 and CTRP7. Mol Cell Endocrinol. 2007 Oct 15;277 (1-2):26-34

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– Tekin S, Erden Y, Ozyalin F, Cigremis Y, Colak C, Sandal S. The effects of intracerebroventricular infusion of irisin on feeding behaviour in rats. Neurosci Lett. 2017 Apr 3;645:25-32. doi: 10.1016/j.neulet.2017.02.066

– Tinkov AA, Gatiatulina ER, Popova EV, Polyakova VS, Skalnaya AA, Agletdinov EF, Nikonorov AA, Skalny AV. Early High-Fat Feeding Induces Alteration of Trace Element Content in Tissues of Juvenile Male Wistar Rats. Biol Trace Elem Res. 2016 Jun 16;

– Tolman JR, Lephart ED, Setchell KD, Eggett DL, Christensen MJ. Timing of supplementation of selenium and isoflavones determines prostate cancer risk factor reduction in rats. Nutr Metab (Lond). 2008;5:31

– Belemets N, Kobyliak N, Virchenko O, Falalyeyeva T, Olena T, Bodnar P, Savchuk O, Galenova T, Caprnda M, Rodrigo L, Skladany L, Delev D, Opatrilova R, Kruzliak P, Beregova T, Ostapchenko L. Effects of polyphenol compounds melanin on NAFLD/NASH prevention. Biomed Pharmacother. 2017 Apr;88:267-276. doi: 10.1016/j.biopha.2017.01.028

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