GLP-2 (Rat) ELISA. For the quantitative determination of glucagon-like peptide 2 (GLP-2) in rat serum and plasma

Transcription

1 GLP-2 (Rat) ELISA For the quantitative determination of glucagon-like peptide 2 (GLP-2) in rat serum and plasma For Research Use Only. Not For Use In Diagnostic Procedures. Catalog Number: 48-GP2RT-E01 Size: 96 wells Version: September 2, 2014 ALPCO November 3, 2014 C26-G Keewaydin Drive, Salem, NH P: (800) F: (603) ts@alpco.com

2 I. Introduction - Please carefully read all of the package insert before beginning the assay. - The proglucagon gene is expressed in both pancreatic A cells and intestinal L cells. Tissue specific post-translational processing of proglucagon by the prohormone convertase produces the different proglucagon derived peptides (PGDPs) in both the pancreas and intestine. The most notable pancreatic PGDP is glucagon, whereas the intestinal L cells produce several structurally related peptides. These include glucagon-like peptide (GLP)-1 and GLP-2, as well as glicentin and oxyntomodulin, which contain the glucagon sequence in their molecules. Among PGDPs, GLP-2 has recently been found to show intestinal epithelial proliferation. GLP-2 (Rat) ELISA Contents This assay can measure GLP-2 in the range of ) Antibody coated plate 100 ng/ml. 2) Rat GLP-2 standard The assay completes within hours hours. 3) Labeled antigen With one assay, 40 samples can be measured in 4) Rat GLP-2 antibody duplicate. 5) SA-HRP solution Test Sample: rat serum or plasma 6) Substrate buffer Sample Volume: 25 μl 7) OPD tablet The 96-well plate consists of 12 8-well strips. 8) Stop solution The strips can be used separately. 9) Buffer solution Precision and Reproducibility 10) Wash solution (concentrated) Intra-assay CV (%) serum ) Adhesive foil (plate sealers) Inter-assay CV (%) serum Intra-assay CV (%) plasma Inter-assay CV (%) plasma Stability and Storage Store all of the components at 2-8 C. The kit is stable under the condition for19 months from the date of manufacturing. The expiry date is listed on the kit label. II. Characteristics This ELISA kit is used for quantitative determination of rat GLP-2 in serum or plasma samples. This kit is characterized for sensitive quantification, high specificity and no influences with other components in samples. The Rat GLP-2 standard is a highly purified synthetic product. Specificity The ELISA kit has high specificity to rat GLP-2 and shows no cross-reactivity with rat glucagon or rat GLP- 1 within the range of 300 pmol/ml. Test Principle This ELISA kit, for determination of rat GLP-2 in serum or plasma samples, is based on a competitive enzyme immunoassay using the combination of a highly specific antibody to rat GLP-2 and a biotin Page 2 of 7

3 avidin affinity system. The 96-well plate is coated with goat anti-rabbit IgG antibody. Rat GLP-2 standard or samples, labeled antigen, and anti-rat GLP-2 polyclonal antibody are added to the wells for a competitive immunoreaction. After incubation and plate washing, HRP labeled streptavidin (SA-HRP) is added to form HRP labeled streptavidin biotinylated rat GLP-2 antibody complexes on the surface of the wells. Finally, HRP enzyme activity is determined by o-phenylenediamine dihydrochloride (OPD) and the concentration of rat GLP-2 is calculated. III. Composition Component Form Quantity Main Ingredient 1. Antibody coated plate MTP *1 1 plate (96 wells) Goat anti-rabbit IgG 2. Rat GLP-2 standard lyophilized 1 vial Synthetic rat GLP-2 (50 ng/vial) 3. Labeled antigen lyophilized 1 vial Biotinylated rat GLP-2 4. Rat GLP-2 antibody liquid 1 bottle (6 ml) Rabbit anti-rat GLP-2 5. SA-HRP solution liquid 1 bottle (12 ml) HRP labeled streptavidin 6. Substrate buffer liquid 1 bottle (26 ml) 0.015% hydrogen peroxide 7. OPD tablet tablet 2 tablets o-phenylenediamine hydrochloride 8. Stop solution liquid 1 bottle (12 ml) 1M H 2SO 4 9. Buffer solution liquid 1 bottle (25 ml) Tris-HCl buffer 10. Wash solution liquid 1 bottle (50 ml) Concentrated saline (concentrate) 11. Adhesive foil 3 sheets (plate sealers) MTP *1.. Microplate IV. Method Equipment required 1) Photometer for microplate (plate reader) which can read optical density of 2.5 at 490 nm 2) Microplate shaker 3) Washing device for microplate and dispenser with aspiration system 4) Micropipettes, multi-channel pipettes for 8 wells or 12 wells, and their tips 5) Test tubes for preparation of Standard solution Page 3 of 7

4 6) Graduated cylinder (1,000 ml) 7) Distilled water or deionized water Preparatory work 1) Preparation of Standard solution: Reconstitute the Standard (lyophilized rat GLP-2 50 ng/vial) with 0.5 ml of Buffer solution, which yields the 100 ng/ml Standard solution. Take 0.1 ml of the reconstituted Standard solution and dilute with 0.2 ml of Buffer solution to product the ng/ml Standard solution. Repeat the same dilution to make the 11.11, 3.704, 1.235, 0.412, and ng/ml Standards. Buffer solution is used as the 0 ng/ml Standard. 2) Preparation of Labeled antigen: Reconstitute Labeled antigen with 9 ml of Buffer solution. 3) Preparation of Substrate solution: Resolve OPD tablet with 12 ml of Substrate buffer. It should be prepared immediately before use. 4) Preparation of Wash solution : Dilute 50 ml of wash solution (concentrated) to 1,000 ml with distilled or deionized water. 5) Other reagents are ready for use. Procedure 1. Allow all reagents and samples to return to room temperature before beginning the test. 2. Fill 75 μl of Labeled antigen solution into the wells first, then introduce 25 μl of the Standards (0, 0.137, 0.412, 1.235, 3.704, 11.11, 33.33, and 100 ng/ml) and the samples, and finally add 50 μl of Rat GLP-2 antibody to the wells. 3. Cover the plate with adhesive foil and incubate it at 4ºC for hours. (The plate shaker is not used for this incubation.) 4. Take off the adhesive foil, aspirate, and wash the wells three times with approximately 0.35 ml/well of wash solution. Finally, invert the plate and tap it onto an absorbent surface, such as paper towels, to ensure blotting free of most residual wash solution. 5. Pipette 100 μl of SA-HRP solution into the wells. Page 4 of 7

5 6. Cover the plate with adhesive foil and incubate it at room temperature (20-30 º C) for 1 hour. During the incubation, the plate should be shaken with a plate shaker. 7. Take off the adhesive foil, aspirate, and wash the wells five times with approximately 0.35 ml/well of wash solution. Finally, invert the plate and tap it onto an absorbent surface, such as paper towels, to ensure blotting free of most residual wash solution. 8. Dissolve OPD tablet with 12 ml of Substrate buffer. It should be prepared immediately before use. 9. Add 100 μl of Substrate solution to the wells, cover the plate with adhesive foil, and incubate it for 30 minutes at room temperature. (The plate shaker is not used for this incubation.) 10. Add 100 μl of stop solution to the wells to stop the color reaction. 11. Read the optical density of the wells at 490 nm. Calculate mean absorbance values of wells containing Standards and plot a standard curve on semilogarithmic graph paper (abscissa: concentration of standard; ordinate: absorbance values.). Use the standard curve to read rat GLP- 2 concentrations of the samples from the corresponding absorbance values. V. Notes 1. Plasma and serum samples must be used as soon as possible after collection. If the samples are to be tested at a later time, they should be frozen in aliquots at or below 30 C. Avoid repeated freezing and thawing of plasma and serum samples. 2. Rat GLP-2 standard, Labeled antigen, and Substrate solution should be prepared immediately before use. The well strips can be divided and used at separate times. In such instances, any remaining volume of the reconstituted reagents (Rat GLP-2 Standard, Labeled antigen) should be stored below -30 C. 3. During storage of wash solution (concentrated) at 2-8 C, precipitates may be observed. The precipitates will dissolve during the dilution of the concentrate. Diluted Wash solution is stable for 6 months at 2-8 C. 4. Pipetting operations may affect the precision of the assay; precisely pipette standard solutions and samples into each well of the plate. Use a new tip for each sample and standard to avoid cross contamination. Use clean test tubes or vessels in assay. 5. When a sample value exceeds 100 ng/ml, the sample needs to be diluted with buffer solution to an appropriate concentration. 6. During incubation except the case at 4 C and color reaction, the plate should be shaken gently with a microtiter plate shaker to promote immunoreaction. Page 5 of 7

6 7. Perform all the determinations in duplicate. 8. Read optical absorbance of reaction solution in the wells immediately after stopping color reaction. 9. To quantify accurately, always run a standard curve when testing samples. 10. Protect reagents from strong light (e.g., direct sunlight) during storage and assay. 11. Satisfactory performance of the test is guaranteed only when reagents from the same lot number are used. VI. Performance Characteristics Typical standard curve OD490- ABS (ng/m l) Analytical recovery Rat serum Sample Rat GLP-2 added Observed Expected* Recovery No. ng/ml ng/ml ng/ml (%) Page 6 of 7

7 Rat plasma Sample Rat GLP-2 added Observed Expected* Recovery No. ng/ml ng/ml ng/ml (%) *Adjusted for spike volume. Precision and reproducibility Intra-assay/Rat serum CV (%) Inter-assay/Rat serum CV (%) Intra-assay/Rat plasma CV (%) Inter-assay/Rat plasma CV (%) Assay Range ng/ml VII. Stability and Storage Storage Store all components at 2-8 C. Shelf life The kit is stable under the condition for 19 months from the date of manufacturing. The expiry date is on the kit label. Package For 96 tests per one kit including standards. VIII. References 1. Philippe, J.: Structure and pancreatic expression of the insulin and glucagon gene. Endocr Rev 12: , Mojsov S. et al: Preproglucagon gene expression in pancreas and intestine diversifies the level of post-transcriptiona processing. J Biol Chem 261: , Drucker, D. J. et al: Induction of intestinal epithelial proliferation by glucagon-like peptide 2. Proc Natl Acad Sci USA 93: , 1996 Page 7 of 7