GlucagonLike Peptide 1 EIA KIT - Cosmo Bio Co.,Ltd.

Antibodies

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GlucagonLike Peptide 1 EIA KIT

Catalog No.: YII-YK160-EX
Size: 1KIT
Price: ¥76000
$1014
antigen/source: GLP-1
catalog info: Catalog 2012-p111
Storage: 4C
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Reacts with: Rat
Human
Mouse
Measurement Range: 0.206 - 50 ng/mL
Purpose: This EIA kit is used for quantitative determination of rat/mouse/human GLP-1 in plasma samples. The kit is characterized by sensitive quantification and high specificity. In addition, it is not influenced by other constituents in samples. GLP-1 standard of this kit is a highly purified synthetic product.
component: Antibody: X
Plate: X
Coating: X
Control: -
Standard: X
Labeling: X
Substrate: X
Others: X
1. Antibody coated plate 1 plate (96 wells)
2. GLP-1 standard 1 vial(25 ng )
3. Labeled antigen 1 vial
4. GLP-1 antibody 1 bottle (6 mL )
5. SA-HRP 1 tube (0.2 mL)
6. Diluent for SA-HRP 1 bottle (12 mL )
7. Substrate buffer 1 bottle (26 mL )
6. OPD tablet 2 tablets
8. OPD tablet 2 tablets
9. Stopping solution 1 bottle (12 mL )
10. Buffer solution 1 bottle (10 mL )
11. Washing solution 1 bottle (50 mL )
21. Adhesive foil 3 sheets

Other:

 Supplementary 
Competitive
 Applicable sample 
Plasma
[Other]
GLP-1 is a peptide hormone from the intestinal mucosa, which is produced from its precursor, proglucagon by post transnational processing. The mammalian proglucagon is synthesized in the neuroendocrine L-cell of the intestine and the alpha-cells of the pancreas. It contains within its structure the sequences of glucagon and two glucagon-like peptides (GLP-1 and GLP-2) in tandem flanked at their amino and carboxyl termini by dibasic residues. GLP-1 is a 37 amino acids peptide and produced in the small intestine and in the pancreas in the human, in either C-terminal-amidated on glycine-extended form.
GLP1 (7-36) amide and its receptor are present in several brain regions and may play a role in the physiological control of feeding. Several reports have been presented as follows as to the biological activities of GLP-1. GLP-1 (7-37) and (7-36) amide is known as one of the most potent insulin secretagogues.
GLP-1 (7-36) amide was supposed to improved glycemic control in patients with type 2 diabetes by increasing insulin secretion, by inhibiting glucagon secretion and by delaying gastric emptying rather than by altering extrapancreatic glucose metabolism. Intravenous GLP-1(7-37) and (7-36)amide could normalize fasting hyperglycaemia in type 2 diabetic patients. Hyperglycaemia during parenteral nutrition could be controlled by exogenous GLP-1, whereas the chronic therapy of type 2 diabetes required GLP-1 derivatives with longer duration of action. Recombinant GLP-1 (7-36) amide was recently shown to cause significant weight loss in type 2 diabetics when administered for 6 weeks as a continuous subcutaneous infusion, 5-day treatment of hereby obese human subjects with GLP-1 at high doses by prandial subcutaneous infusion promptly slowed gastric emptying as a probable mechanism of action of increased satiety, decreased hunger and reduced food intake with an ensuing weight loss.
A G-protein-coupled receptor, GPR120, which is abundantly expressed in intestine, functions as a receptor for unsaturated long-chain FFAs (free fatty acids). The stimulation of GPR120 by FFAs promotes the secretion of GLP-1 in vitro (measured by YK160, Yanaihara Institute Inc) and in vivo, and increases circulation insulin, indicate that GPR120-mediated GLP-1 secretion induced by dietary FFAs is important in the treatment of diabete.
All these approaches have shown remarkable efficacy in both experimental and clinicalstudies. The GLP-1-based therapy of type 2 diabetes, therefore, represents a new and attractive alternative.


Reference:

•  Fukunaga T, Sasaki M, Araki Y, Okamoto T, Yasuoka T, Tsujikawa T, Fujiyama Y, Bamba T. Digestion. 2003;67(1-2):42-9.
•  Hirotani Y, Yamamoto K, Ikeda K, Arakawa Y, Li J, Kitamura K, Kurokawa N, Tanaka K. Biol Pharm Bull. 2006 Nov;29(11):2327-30.
•  Hirotani Y, Ikeda T, Ikeda K, Yamamoto K, Onda M, Arakawa Y, Li J, Kitamura K, Kurokawa N. Yakugaku Zasshi. 2007 Sep;127(9):1509-13.
•  Izumi H, Ishizuka S, Inafune A, Hira T, Ozawa K, Shimizu T, Takase M, Hara H. J Nutr. 2009 Jul;139(7):1322-7. Epub 2009 Jun 3.
•  Nutr Res. 2011 Sep;31(9):707-14.
◊  Nutr Res. 2011 Sep;31(9):707-14.
 
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