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Description
Mouse CNR1 ELISA KitProduct Specification Usage Experimental equipment required for the experiment: 1. Microplate reader (450nm) 2. High precision pipette and gun tips: 0. 5 10uL, 5 50uL, 20 200uL, 200 1000uL 3. 37 constant temperature box 4. Distilled water or deionized water Sample processing and requirements: Serum: Place the whole blood sample collected in the serum separation tube at room temperature for 2 hours or at 4 overnight, then centrifuge at 1000g for 20
Product Specification
| Usage |
Experimental equipment required for the experiment: 1. Microplate reader (450nm) 2. High-precision pipette and gun tips: 0.5-10uL, 5-50uL, 20-200uL, 200-1000uL 3. 37℃ constant temperature box 4. Distilled water or deionized water Sample processing and requirements: Serum: Place the whole blood sample collected in the serum separation tube at room temperature for 2 hours or at 4℃ overnight, then centrifuge at 1000×g for 20 minutes, and take the supernatant, or store the supernatant at -20℃ or -80℃, but avoid repeated freezing and thawing. Plasma: Collect specimens using EDTA or heparin as an anticoagulant and centrifuge at 1000×g for 15 minutes at 2-8°C within 30 minutes of collection. Remove the supernatant for testing, or store at -20°C or -80°C, but avoid repeated freezing and thawing. Cell culture supernatant: Centrifuge at 1000×g for 20 minutes. Remove the supernatant for testing, or store at -20°C or -80°C, but avoid repeated freezing and thawing. Pre-Test Preparation: 1. Remove the test kit from the refrigerator 10 minutes in advance and equilibrate to room temperature. 2. Prepare a gradient standard working solution: Add 1 mL of universal diluent to the lyophilized standard. Let stand for 15 minutes to completely dissolve, then gently mix (concentration 20 ng/mL). Then dilute to the following concentrations: 20 ng/mL, 10 ng/mL, 5 ng/mL, 2.5 ng/mL, 1.25 ng/mL, 0.625 ng/mL, 0.3125 ng/mL, and 0 ng/mL. Serial dilution method: Take seven EP tubes and add 500 μL of universal diluent to each tube. Pipette 500 μL of the 20 ng/mL standard working solution into the first EP tube and mix thoroughly to make a 10 ng/mL standard working solution. Repeat this procedure for subsequent tubes. The last tube serves as a blank well; there is no need to pipette liquid from the penultimate tube. See the figure below for details. 3. Preparation of biotinylated detection antibody working solution: Centrifuge the concentrated biotinylated antibody at 1000×g for 1 minute 15 minutes before use. Dilute the 100× concentrated biotinylated antibody to a 1× working concentration with universal diluent (e.g., 10uL concentrate + 990uL universal diluent). Prepare and use immediately. 4. Prepare the enzyme conjugate working solution: 15 minutes before use, centrifuge the 100× concentrated enzyme conjugate at 1000×g for 1 minute. Dilute the 100× concentrated HRP enzyme conjugate to a 1× working concentration with universal diluent (e.g., 10 μL of concentrate + 990 μL of universal diluent). Prepare immediately. 5. Prepare the 1× wash solution: Dispense 10 mL of 20× wash solution into 190 mL of distilled water (concentrated wash solution removed from the refrigerator may crystallize; this is normal. Allow to stand at room temperature until the crystals have completely dissolved before preparing). Procedure: 1. Remove the desired strips from the aluminum foil bag after equilibration at room temperature for 10 minutes. Seal the remaining strips in a ziplock bag and return to 4°C. 2. Sample addition: Add 100 μL of sample or standard of varying concentrations to the corresponding wells. Add 100 μL of universal diluent to the blank wells. Cover with a film and incubate at 37°C for 60 minutes. (Recommendation: Dilute the sample to be tested at least 1-fold with universal diluent before adding it to the ELISA plate. This will reduce the impact of matrix effects on the test results. The sample concentration should be multiplied by the corresponding dilution factor when calculating the final sample concentration. It is recommended to run replicates for all test samples and standards.) 3. Add Biotinylated Antibody: Remove the ELISA plate and discard the liquid without washing. Add 100 μL of Biotinylated Antibody Working Solution directly to each well. Cover with a film and incubate at 37°C for 60 minutes. 4. Wash: Discard the liquid and add 300 μL of 1x Wash Solution to each well. Let stand for 1 minute, shake off the wash solution, and pat dry on absorbent paper. Repeat this process three times (a plate washer can also be used). 5. Add Enzyme Conjugate Working Solution: Add 100 μL of Enzyme Conjugate Working Solution to each well. Cover with a film and incubate at 37°C for 30 minutes. 6. Washing: Discard the liquid and wash the plate five times as in step 4. 7. Adding substrate: Add 90 μL of substrate (TMB) to each well, cover with a sealing film, and incubate at 37°C in the dark for 15 minutes. 8. Adding stop solution: Remove the ELISA plate and add 50 μL of stop solution directly to each well. Immediately measure the OD value of each well at a wavelength of 450 nm. Calculating experimental results: 1. Calculate the average OD value of the standard and sample replicates and subtract the OD value of the blank well as a correction factor. Plot the standard curve of the four-parameter logistic function on double-logarithmic graph paper, with concentration as the horizontal axis and OD value as the vertical axis. 2. If the sample OD value is higher than the upper limit of the standard curve, dilute the sample appropriately and retest. Multiply the sample concentration by the corresponding dilution factor. |
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| Theory | This kit uses a double-antibody sandwich enzyme-linked immunosorbent assay (ELISA). Sample, standard, biotin-labeled detection antibody, and HRP conjugate are sequentially added to microwells pre-coated with a capture antibody against Cannabinoid Receptor 1, Brain (CNR1). After incubation and washing, the sample is developed using the substrate TMB. TMB is converted to blue by peroxidase (HRP) catalysis and to yellow by acid. The intensity of the color is positively correlated with the amount of Cannabinoid Receptor 1, Brain (CNR1) in the sample. The absorbance (OD) is measured at 450 nm using a microplate reader to calculate the sample concentration. | |||||||||||||||||||||||||||||||||
| Source | Mouse | |||||||||||||||||||||||||||||||||
| Synonym | Mouse Cannabinoid Receptor 1, Brain ELISA Kit | |||||||||||||||||||||||||||||||||
| Detection Type | Double antibody sandwich method | |||||||||||||||||||||||||||||||||
| Composition |
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| Background | Cannabinoid receptor type 1, also known as cannabinoid receptor 1, is a G protein-coupled cannabinoid receptor encoded by the CNR1 gene. Disorders associated with CNR1 include cannabis dependence and abuse. Pathways involved in this gene include peptide ligand binding to receptors and GPCR signaling. Gene Ontology (GO) annotations associated with this gene include G protein-coupled receptor activity and cannabinoid receptor activity. An important homologue of this gene is CNR2. | |||||||||||||||||||||||||||||||||
| General Notes | 1. Strictly adhere to the specified incubation time and temperature to ensure accurate results. All reagents must be at room temperature (20-25°C) before use. Refrigerate reagents immediately after use. 2. Improper plate washing may result in inaccurate results. Ensure that all liquid in the wells is aspirated thoroughly before adding substrate. Do not allow the wells to dry out during incubation. 3. Remove any residual liquid and fingerprints from the bottom of the plate, as this will affect the OD value. 4. The substrate developer solution should be colorless or very light in color. Do not use substrate solution that has turned blue. 5. Avoid cross-contamination of reagents and specimens to prevent erroneous results. 6. Avoid direct exposure to strong light during storage and incubation. 7. Do not expose any reagents to bleaching solvents or the strong fumes emitted by bleaching solvents. Any bleaching agent will destroy the biological activity of the reagents in the kit. 8. Do not use expired products, and do not mix components with different product numbers and batches. 9. Recombinant proteins from sources other than the kit may not be compatible with the antibodies in this kit and will not be recognized. 10. If there is a possibility of disease transmission, all samples should be managed properly and samples and testing devices should be handled according to prescribed procedures. |
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| Storage Temp. | If the unopened kit is stored at 4°C, the shelf life is 6 months. | |||||||||||||||||||||||||||||||||
| Test Range | 0.312-20 ng/mL | |||||||||||||||||||||||||||||||||
| Applications | Serum, plasma, cell culture supernatant |
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4.3 ★★★★★
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Product Reviews
★★★★★ 5
Love these!
Size: 50 count (Pack of 1)
Leaves my face feeling fresh and clean. Doesn't leave any type of film behind
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Reviewed in the United States on May 25, 2026
★★★★★ 5
Great product with unexpected results and skincare benefits
Size: 25 Count (Pack of 1)
I have been reading about Micellar water products for a couple of years, and finally purchased these wipes to try. I am currently working very long hours and the selling point for these wipes was that they weren't soap-based, and didn't require a toner after using. I keep them on my night stand and take my makeup off with them prior to going to bed. (I do not use them for removing mascara - I use another product for that.)
The biggest point I want to share is that I have been using these wipes exclusively for makeup removal for a little more than two weeks. I have had a stubborn blackhead on my nose for a good 20 years that wouldn't budge, no matter how often I used exfoliating products, and I've invested a lot of money in high end exfoliators in an attempt to make that spot go away. It has grown larger over the years, and was a skincare peeve of mine. I noticed a couple of days ago that that blackhead is beginning to break down and get smaller. I thought at first that I was imagining it, but that blackhead is honestly a good two-thirds gone. This is just from using these wipes! I would never have predicted that something this simple and quite soft and insubstantial as a disposable face wipe would have such effective results for blackhead breakdown, but they're doing the trick. I have noticed smaller blackheads on my chin area are also melting away. I predict that in another few weeks of use, my skin is going to be as close to blackhead-free as it is humanly possible to achieve. (For the record, I don't have a lot of blackheads - just a handful that have taken up residence over the years and refused to budge, getting larger with age.)
These are safe for my sensitive skin, and have exfoliating benefits that I wouldn't ever have expected or predicted. Full disclosure: I do spend a good 3-5 minutes using a single wipe on my face, neck, and décolletage, scrubbing with the nubby side (there is a nubby, exfoliating side, and smooth side to each wipe) and using the whole cloth in sections until I have used it all. Finally, I also use it on the tops of my hands. I definitely get my money's worth out of each wipe! I wholeheartedly encourage people to try this product. I now have it on Auto-Ship status, as I don't want to ever be without these wipes in my skincare arsenal.
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Reviewed in the United States on May 23, 2016
★★★★★ 5
Cool and moist
Size: 1 Count (Pack of 2)
I had to get away from scented products and this one was cleared by my ACDS app. It is small, not resealable, but easy to use, and cleans well, the wipes are sturdy, and just wet enough to clean without needing extra drying. These are travel size and have to be kept in a zip lock after opening.
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Reviewed in the United States on December 25, 2025
★★★★★ 5
Best wipes
Best on the market
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Reviewed in the United States on March 26, 2026
★★★★★ 4
GENTLE TO SKIN
Size: 25 Count (Pack of 1)
These cleansing wipes are really gentle and effective at removing my makeup without any irritation. I appreciate how quick and convenient they are for my skincare routine.
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Reviewed in the United States on June 21, 2025