Human CD3 ELISA Kit For the quantitative in vitro determination of Human CD 3 concentrations in serum - plasma - celiac fluid - tissue homogenate - body fluid FOR LABORATORY RESEARCH USE ONLY. NOT FOR USE IN DIAGNOSTIC PROCEDURES. This package insert must be read in its entirety Before using this product. ELISAENZYME LINKED IMMUNOSORBENT ASSAYINTENDED USE AND TEST PRINCIPLEThis CD3 ELISA kit is intended Laboratory for Research use only and is not for use in diagnostic or therapeutic procedures. The Stop Solution changes the color from blue to yellow and the intensity of the color The measured standards are at the same time as the samples and allow the operator to produce a concentration curve of Optical Density versus CD3 concentration. The concentration of CD3 in the samples is then determined by comparing the OD SAMPLE COLLECTION AND STORAGESSerum - Use a serum separator tube and allow samples to clot for 2 hours at room temperature or overnight at 4°C before centrifugation for 20 minutes at approximately 2000×g. Remove serum and assay immediately Or aliquot and store samples at -20°C. Avoiding freeze-thaw cyclesPlasma - Collect plasma using heparin as an anticoagulant. Centrifuge samples for 30 minutes at 2000×g at 2-8°C within 30 minutes of collection. Store samples at -20 °C. Avoiding freeze-thaw cycles.Cell culture supernates, tissue homogenate and other biological fluids - Remove particulates by centrifugation and assay immediately or aliquot and store samples at -20°C. Avoiding freeze-thaw cycles.Note: The samples shoule be Centrifugated dequately and no hemolysis or granule was allowed.MATERIALS REQUIRED BUT NOT SUPPLIED1. 37 °C incubator2. Standard microplate reader capable of measuring absorbance at 450 nm3. Precision pipet TER, disposable pipette tips and Absorbent paper4. Distilled or deionized waterREAGENTS PROVIDED All reagents provided are stored at 2-8°C. Refer to the expiration date on the label. Name 96 determinations 48 determinationsMicroelisa stripplate 12*8strips 12*4stripsStandard(6 vial 0.5ml/vial 0.5ml/vialSample diluent 6.0ml 3.0mlHRP-Conjugate reagent 10.0ml 5.0ml20X Wash solution 25ml 15mlChromogen Solution A 6.0ml 3.0mlChromogen Solution B 6.0ml 3.0mlStop Solution 6.0ml 3.0mlClosure plate membrane 2 2User manual 1 1Sealed bags 1 1Note: 1. Standard concentration was followed by: 100, 50, 25, 12.5, 6.25, 3.12 ng/mL2. If samples generate values ​​higher than the highest standard, please dilute the samples with Sample Diluent and repeat the assay.PRECAUTIONS1. 2. Do not substitute reagents from one kit lot to another. Standard, conjugate and microtiter plates are matched for optimal performance. Use only the reagents supplied by manufacturer. 2. Allow kit reagents and materials to rea 5. do not use water baths to thaw samples or reagents. 3. Do not use kit components beyond their expiration date. 4. Use only deionized or distilled water to dilute reagents. Do not remove microtiter plate from the storage bag until needed. Unused strips should be stored at 2-8°C in their pouch with the desiccant provided. 6. Use fresh disposable pipette tips for each transfer to avoid contamination. 7. Do not mix Disposable knives must be subjected to the assay procedure, since no known test method can offer complete assurance that products derived from Rat blood will not Transmitted infectious agents. Therefore, all blood derivatives should be considered potentially infectious and good laboratory practices should be followed. 9. All samples should be disposed of in a manner that will inactivate viruses. Liquid Waste: Add sodium hypochlorite to a final concentration of 1.0%. The waste should be allowed to stand for a minimum of 30 minutes to inactivate the viruses before disposal. 11. Substrate Solution is easily contaminated. If bluish prior to use, do not Use. 12. Substrate B contain 20% acetone, keep this reagent away from sources of heat or flame. 13. Remove all kit reagents from refrigerator and allow them to reach room temperature ( 20-25°C).REAGENT PREPARATION AND STORAGEWash Solution (1X) - Dilute 1 volume of Wash solution (20X) with 19 volumes of deionized or distilled water. Wash Solution is stable for 1 month at 2-8°C. ASSAY PROCEDURE1. Prepare all reagents before starting assay procedure. It is recommended That all Standards and Samples be added in duplicate to the Microelisa Stripplate.2. Add 50μl of Standard or Sample to the appropriate wells. Blank well doesn't add anyting.3. Add 100μl of HRP-conjugate reagent to standard wells and sample wells Except the blank well Wash the Microtiter Plate 4 times. Manual Washing - Remove incubation mixture by aspirating contents of the plate into a sink or proper waste container. Using a squirt bottle, cover with an adhesive strip and incubate for 60 minutes at 37°C.4. Fill each well completely with Wash Solution (1X), then aspirate contents of the plate into a sink or proper waste container. Repeat this procedure for a total of four times. After final wash, invert plate, and blot dry by hitting plate Note: Hold the sides of the plate frame firm when washing the plate to assure that all strips remain securely in frame. Automated Washing - Aspirate all wells, then wash plates four times using Wash Buffer (1X Always support your friend to aspirate as much liquid as possible and set fill volume at 350μL/well/wash. After final wash, invert plate, and blot dry by hitting plate. Add c Hromogen solution A 50μl and chromogen solution B 50μl to each well. Gently mix and incubate for 15 minutes at 37°C. Protect from light.6. Add 50μl Stop Solution to each well. The color in the wells should change from blue to yellow Read the Optical Density (OD) at 450 nm using a microtiter plate reader within 15 minutes.CALCULATION OF The standard curve is generated by plotting the average OD (450 nm) obtained for each of the six standard concentrations on the vertical (X) axis versus the corresponding concentration on 2. The first OD values ​​are subtracted by the mean value of the balnk well before result interpretation. Construct the standard curve using graph paper or statistical softw At the point of intersection, draw a vertical line to the X-axis and read the 4. Any variation in operator, pipetting and washing technique, incubation time or temperature, and kit age can cause variation in result. Each user should obtain their own standard curve.5. Intra-assay CV(%) and Inter- Assay range: 3.12 ng/ml –100 ng/ml.7. Sensitivity: The minimum detectable dose of Human CD3 is typically less than 1.0 ng/ml8. Cross-reactivity: This assay recognizes recombinant and natural Human CD3. No significant cross-reactivity or interference was observed. 9. Storage: 2-8 ° C (Use frequently); six months (-20 ° C). 10. QUOTE READ ONH;
The 100% pure wood pulp Kitchen Paper Towel is both water and oil absorbent, making it suitable for use in the kitchen.
Along with kitchen paper products in standard sizes, produce custom kitchen towels according to customer requirements.
This Kitchen Paper Towel can easily absorb residual grease from frying foods.
Before cooking eat or fish, use the Kitchen Paper Towel to absorb the water on the surface, thus preventing hot oil splashes when placing the food into the pan.
By absorbing grease on tableware with the Kitchen Paper Towel, users can effectively reduce the need for expensive cleaning agents.
This kitchen towel is ideal for cleaning cooking equipment, dining room tables and tableware.
Kitchen Tissue Roll,Kitchen Towel Tissue,Kitchen Tissue Paper,Kitchen Tissue Paper Roll
Yafeng Paper Industry Co., Ltd , https://www.tenoutissue.com