Exendin (9-39) amide, GLP-1 receptor antagonist (ab141101)
Key features and details
- Potent, selective GLP-1 receptor antagonist
- CAS Number: 133514-43-9
- Purity: > 98%
- Soluble in water to 1mg/ml
- Form / State: Solid
- Source: Synthetic
製品の概要
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製品名
Exendin (9-39) amide, GLP-1 receptor antagonist -
製品の詳細
Potent, selective GLP-1 receptor antagonist -
生理活性の詳細
Potent, selective GLP-1 receptor antagonist (Kd = 1.7 nM). Inhibits the generation of intracellular cAMP induced by GLP-1 (7-36), exendin-3 and exendin-4 (ab120214). Role in appetite modulation, water and salt homeostasis and insulin release. Active in vivo.
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精製度
> 98% -
CAS 番号
133514-43-9 -
構造式
製品の特性
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分子量
3369.79 -
分子式
C149H234N40O47S -
配列
DLSKQMEEEAVRLFIEWLKNGGPSSGAPPPS (Modifications: C-terminal amide) -
PubChem 登録番号
129012199 -
保存方法
Store at -20°C. Store under desiccating conditions. The product can be stored for up to 12 months. -
溶解性
Soluble in water to 1mg/ml -
使用に関する注意
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one week. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour.
Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
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由来
Synthetic
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研究分野
プロトコール
To our knowledge, customised protocols are not required for this product. Please try the standard protocols listed below and let us know how you get on.
参考文献 (7)
ab141101 は 7 報の論文で使用されています。
- Saitoh Y et al. Improvement of hepatocyte engraftment by co-transplantation with pancreatic islets in hepatocyte transplantation. J Tissue Eng Regen Med 15:361-374 (2021). PubMed: 33484496
- Ohbayashi K et al. Gastrointestinal Distension by Pectin-Containing Carbonated Solution Suppresses Food Intake and Enhances Glucose Tolerance via GLP-1 Secretion and Vagal Afferent Activation. Front Endocrinol (Lausanne) 12:676869 (2021). PubMed: 34168616
- Tu Y et al. Geniposide Attenuates Hyperglycemia-Induced Oxidative Stress and Inflammation by Activating the Nrf2 Signaling Pathway in Experimental Diabetic Retinopathy. Oxid Med Cell Longev 2021:9247947 (2021). PubMed: 34938383
- Okabe K et al. DPP (Dipeptidyl Peptidase)-4 Inhibitor Attenuates Ang II (Angiotensin II)-Induced Cardiac Hypertrophy via GLP (Glucagon-Like Peptide)-1-Dependent Suppression of Nox (Nicotinamide Adenine Dinucleotide Phosphate Oxidase) 4-HDAC (Histone Deacetylase) 4 Pathway. Hypertension 75:991-1001 (2020). PubMed: 32160098
- Kim KH et al. Cucurbitacin B Induces Hypoglycemic Effect in Diabetic Mice by Regulation of AMP-Activated Protein Kinase Alpha and Glucagon-Like Peptide-1 via Bitter Taste Receptor Signaling. Front Pharmacol 9:1071 (2018). PubMed: 30298009
- Kim KS et al. Activation of intestinal olfactory receptor stimulates glucagon-like peptide-1 secretion in enteroendocrine cells and attenuates hyperglycemia in type 2 diabetic mice. Sci Rep 7:13978 (2017). PubMed: 29070885
- Hwang I et al. Alteration of gut microbiota by vancomycin and bacitracin improves insulin resistance via glucagon-like peptide 1 in diet-induced obesity. FASEB J 29:2397-411 (2015). PubMed: 25713030