Mouse PFP ELISA Kit For the quantitative in vitro determination of Mouse Pore-forming protein 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 The ELISA kit is exemplified by the ELISA kit. The ELISA kit is intended to be used by the laboratory. The Stop Solution changes the color from blue to yellow and the intensity of the In order to measure the concentration of PFP in the sample, the PFP ELISA Kit includes a set of calibration standards. The calibration standards are assayed at the same time as the samples and allow the operator to Produce a standard curve of Optical Density versus PFP concentration. The concentration of PFP in the samples is then determined by co Mparing the OD of the samples to the standard curve. 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. 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. 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. 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 pipettes, 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: 1000, 500, 250, 125, 62.5, 31.2 pg/ml2. If samples generate values ​​higher than the highest standard, please dilute the samples with Sample Diluent and repeat the assay.PRECAUTIONS1 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 reach room temperature (20-25°C) before use. 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. 5. 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 Disposable knuckles must during the assay procedure, since no known test method can offer complete assurance that products derived from Mouse blood Will not transmit 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 inac 11. 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 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 Add to the micro-lisa stripplate.2. Add 50μl of Standard or Sample to the appropriate wells Standard wells and sample wells ex Cept the blank well, cover with an adhesive strip and incubate for 60 minutes at 37°C.4. Wash the Microtiter Plate 4 times. Manual Washing - Remove incubation mixture by aspirating contents of the plate into a sink or proper waste container. a squirt bottle, 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 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 Maintain Buffer (1X). Always adjust your brush 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 mount absorbent paper or paper blanket until no moistu Add chromogen 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 Read the Optical Density (OD) at 450 nm using a microtiter plate reader The standard curve is generated by plotting the average OD (450 nm) obtained for each of the six standard concentrations on the vertical (X) 2. First, calculate the mean OD value for each standard and sample. All OD Values ​​are subtracted by the mean value of the balnk well before result interpretation. Construct the standard curve using Graph paper o r statistical software. 3. To determine the amount in each sample, first locate the OD value on the Y-axis and extend a horizontal line to the standard curve. At the point of intersection, draw a vertical line to the X-axis and 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 CV (%) are less than 15%.6. Assay range: 31.2 pg/ml –1000pg/ml.7. Sensitivity: The minimum detectable dose of Mouse PFP is typically less than. 1.0 pg/ml8. Cross- No particular cross-reactivity or interference was observed. 9. Storage: 2-8 ° C (Use frequently); six months (-20 ° C). 10. QUOTE READ ONH;
Primer mainly used to make up for uneven skin color, dark shortcomings, local use can make the skin be modified, showing crystal clear natural luster. It is the cosmetics used before makeup, usually emulsion, white, transparent, light green, lavender, pink and so on.
Benefits:Refine skin tone, refine pores, and smooth skin.
Product Usage:The makeup primer is known as the double-sided tape for make-up. It can adjust the skin tone and make the base makeup fit the skin.
Selection skills:1.Mixed and oily skin: Since the face is prone to oil, it is difficult to achieve a flawless nude makeup effect without effective oil control. Therefore, if people with this skin type choose a makeup primer, they must first choose an oil-free formula, especially if they cannot Choose bright products. Because of the oil, the face is easy to shine, and the forehead and T-zone appear shiny. If pearl products are used again, the oil will be more obvious and affect the appearance. 2.Normal and dry skin: People with normal and dry skin are more troublesome when choosing, because the skin is relatively dry, so they need more moisturizing products, such products are more delicate and easy to absorb. Because the skin is relatively dry, it is easier to grow wrinkles, and the skin's elasticity is relatively poor. Therefore, only by choosing this highly moisturizing product can the skin be effectively protected.
Primer,The Primer,A Primer,Best Primer
Guangzhou Natural Beauty Cosmetics Co;Ltd , https://www.artmissnatural.com