GLP-1 ELISA Kit

Produktnummer ABIN6956106

Produktdetails GLP-1 ELISA Kit

Target: GLP-1 (Glucagon-like peptide 1 (GLP-1))

Reaktivität: Human, Maus, Ratte, Hund, Rind (Kuh), Kaninchen

Nachweismethode: Colorimetric

Methodentyp: Competition ELISA

Detektionsbereich: 12.35 pg/mL - 1000 pg/mL

Untere Nachweisgrenze: 12.35 pg/mL

Applikation: ELISA

Verwendungszweck: The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of GLP1 in serum, plasma. Due to the 100% homology of the sequence among different species, the kit can be used to detect human, mouse, rat, rabbit, bovine and canine samples.

Proben: Plasma, Serum

Analytische Methode: Quantitative

Spezifität: This assay has high sensitivity and excellent specificity for detection of Glucagon Like Peptide 1 (GLP1)

Sensitivität: 4.26 pg/mL

Bestandteile:

• Pre-coated, ready to use 96-well strip plate, flat buttom
• Plate sealer for 96 wells
• Reference Standard
• Standard Diluent
• Detection Reagent A
• Detection Reagent B
• Assay Diluent A
• Assay Diluent B
• Reagent Diluent (if Detection Reagent is lyophilized)
• TMB Substrate
• Stop Solution
• Wash Buffer (30 x concentrate)
• Instruction manual

Anwendungsinformationen

Kommentare:

Information on standard material:
The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

Information on reagents:
The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

Information on antibodies:
The provided antibodies and their host vary in different kits.

Probenmenge: 50 μL

Testdauer: 2 h

Plattentyp: Pre-coated

Protokoll:

1. Prepare all reagents, samples and standards,
2. Add 50μL standard or sample to each well.
   Then add 50μL prepared Detection Reagent A immediately.
   Shake and mix. Incubate 1 hour at 37 °C,
3. Aspirate and wash 3 times,
4. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
5. Aspirate and wash 5 times,
6. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
7. Add 50μL Stop Solution. Read at 450 nm immediately.

Aufbereitung der Reagenzien:

1. Bring all kit components and samples to room temperature (18-25 °C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
2. Standard - Reconstitute the Standard with 2.0 mL of Standard Diluent, kept for 10 minutes at room temperature, shake gently(not to foam). The concentration of the standard in the stock solution is 1,000pg/mL. Please prepare 5 tubes containing 0.6 mL Standard Diluent and produce a triple dilution series according to the picture shown below. Mix each tube thoroughly before the next transfer. Set up 5 points of diluted standard such as 1,000pg/mL, 333.33pg/mL, 111.11pg/mL, 37.04pg/mL, 12.35pg/mL, and the last EP tubes with Standard Diluent is the blank as 0pg/mL.
3. Detection Reagent A and Detection Reagent B - If lyophilized reconstitute the Detection Reagent A with 150μL of Reagent Diluent, kept for 10 minutes at room temperature, shake gently (not to foam). Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
4. Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
5. TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.

Note:

1. Making serial dilution in the wells directly is not permitted.
2. Prepare standard within 15 minutes before assay. Please do not dissolve the reagents at 37 °C directly.
3. Detection Reagent A and B are sticky solutions, therefore, slowly pipette them to reduce the volume errors.
4. Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
5. The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
6. If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
7. Contaminated water or container for reagent preparation will influence the detection result.

Aufbereitung der Proben:

• It is recommended to use fresh samples without long storage, otherwise protein degradation and denaturationmay occur in these samples, leading to false results. Samples should therefore be stored for a short periodat 2 - 8 °C or aliquoted at -20 °C (≤1 month) or -80 °C (≤ 3 months). Repeated freeze-thawcycles should be avoided. Prior to assay, the frozen samples should be slowly thawed and centrifuged toremove precipitates.
• If the sample type is not specified in the instructions, a preliminary test is necessary to determinecompatibility with the kit.
• If a lysis buffer is used to prepare tissue homogenates or cell culture supernatant, there is a possibilityof causing a deviation due to the introduced chemical substance.The recommended dilution factor is for reference only.
• Please estimate the concentration of the samples before performing the test. If the values are not in therange of the standard curve, the optimal sample dilution for the particular experiment has to be determined.Samples should then be diluted with PBS (pH =7.0-7.2).

Testpräzision: Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level of target were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level of target were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV < 10%
Inter-Assay: CV < 12%

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Vorsichtsmaßnahmen: The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.

Lagerung: 4 °C/-20 °C

Informationen zur Lagerung:

1. For unopened kit: All reagents should be stored according to the labels on the vials. The Standard, Detection Reagent A, Detection Reagent B, and 96-well Strip Plate should be stored at -20 °C upon receipt, while the other reagents should be stored at 4 °C.
2. For opened kits: the remaining reagents must be stored according to the above storage conditions. In addition, please return the unused wells to the foil pouch containing the desiccant and seal the foil pouch with the zipper.

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Haltbarkeit: 6 months

Referenzen für GLP-1 ELISA Kit (ABIN6956106)

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Guo, Han, Wang, Zhang, Liu, Zhang, Hu: "miR-200a regulates Rheb-mediated amelioration of insulin resistance after duodenal-jejunal bypass." in: International journal of obesity (2005), Vol. 40, Issue 8, pp. 1222-32, (2018) (PubMed).

Dolo, Yao, Li, Zhu, Shi, Widjaja: "Preserving Duodenal-Jejunal (Foregut) Transit Does Not Impair Glucose Tolerance and Diabetes Remission Following Gastric Bypass in Type 2 Diabetes Sprague-Dawley Rat Model." in: Obesity surgery, Vol. 28, Issue 5, pp. 1313-1320, (2018) (PubMed).

Wu, Yan, Cheng, Zhong, Liu, Zhang, Hu: "Deactivation of the NLRP3 inflammasome in infiltrating macrophages by duodenal-jejunal bypass surgery mediates improvement of beta cell function in type 2 diabetes." in: Metabolism: clinical and experimental, Vol. 81, pp. 1-12, (2018) (PubMed).

Chen, Xia, Liu, He, Zhang: "Selective Vagotomy Worsens Glucose Control After Ileal Transposition." in: Obesity surgery, Vol. 28, Issue 8, pp. 2494-2499, (2018) (PubMed).

Yan, Chen, Zhu, Lin, Pan, Li, Wang, Yang, Liu, Gong: "Ileal Transposition Surgery Decreases Fat Mass and Improves Glucose Metabolism in Diabetic GK Rats: Possible Involvement of FGF21." in: Frontiers in physiology, Vol. 9, pp. 191, (2018) (PubMed).

Wu, Cheng, Huang, Zhong, Liu, Hu: "Downregulation of lncRNA MALAT1 contributes to renal functional improvement after duodenal-jejunal bypass in a diabetic rat model." in: Journal of physiology and biochemistry, Vol. 74, Issue 3, pp. 431-439, (2018) (PubMed).

Zhong, Liu, Zhang, Zhang, Liu, Hu: "Alterations in gut microbiota during remission and recurrence of diabetes after duodenal-jejunal bypass in rats." in: World journal of gastroenterology, Vol. 22, Issue 29, pp. 6706-15, (2016) (PubMed).

Wang, Zhou, Quach, Lu, Gao, Xu, Zhu: "Effect of Sleeve Gastrectomy Plus Side-to-Side Jejunoileal Anastomosis for Type 2 Diabetes Control in an Obese Rat Model." in: Obesity surgery, Vol. 26, Issue 4, pp. 797-804, (2016) (PubMed).

Qi, Ke, Liu, Liao, Ke, Liu, Wang, Lin, Zhou, Wu, Chen, Liu et al.: "Subcutaneous administration of liraglutide ameliorates learning and memory impairment by modulating tau hyperphosphorylation via the glycogen synthase kinase-3β pathway in an amyloid β protein ..." in: European journal of pharmacology, Vol. 783, pp. 23-32, (2016) (PubMed).

Balakumar, Prabhu, Sathishkumar, Prabu, Rokana, Kumar, Raghavan, Soundarajan, Grover, Batish, Mohan, Balasubramanyam: "Improvement in glucose tolerance and insulin sensitivity by probiotic strains of Indian gut origin in high-fat diet-fed C57BL/6J mice." in: European journal of nutrition, (2016) (PubMed).

Bak, Wewer Albrechtsen, Pedersen, Knop, Vilsbøll, Jørgensen, Hartmann, Deacon, Dragsted, Holst: "Specificity and sensitivity of commercially available assays for glucagon-like peptide-1 (GLP-1): implications for GLP-1 measurements in clinical studies." in: Diabetes, obesity & metabolism, Vol. 16, Issue 11, pp. 1155-64, (2015) (PubMed).

Cao, Cao, Liu: "Expression of cholecystokinin2-receptor in rat and human L cells and the stimulation of glucagon-like peptide-1 secretion by gastrin treatment." in: Acta histochemica, Vol. 117, Issue 2, pp. 205-10, (2015) (PubMed).

Hauge-Evans, Bowe, Franklin, Hassan, Jones: "Inhibitory effect of somatostatin on insulin secretion is not mediated via the CNS." in: The Journal of endocrinology, Vol. 225, Issue 1, pp. 19-26, (2015) (PubMed).

Details zu GLP-1

Target: GLP-1 (Glucagon-like peptide 1 (GLP-1))

Andere Bezeichnung: Glucagon Like Peptide 1 (GLP1) (GLP-1 Produkte)

Synonyme: GLP1 ELISA Kit, GLP2 ELISA Kit, GRPP ELISA Kit, GLP-1 ELISA Kit, Glu ELISA Kit, PPG ELISA Kit, glucagon ELISA Kit, GCG ELISA Kit, Gcg ELISA Kit