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Description
Rat TRAP ELISA KitProduct Specification Usage 1. Self prepared test equipment required for the experiment: 1, plate reader (450nm) 2, high precision sampler and gun head: 0. 5 10uL5 50uL20 200uL200 1000uL 3, 37 Incubator 4, Distilled water or deionized water 2. Sample processing and requirements: The detection range of the kit is not equivalent to the concentration range of the test substance in the sample It is recommended to estimate the concentration of the test
Product Specification
| Usage |
1. Self-prepared test equipment required for the experiment: 1, plate reader (450nm) 2, high-precision sampler and gun head: 0.5-10uL、5-50uL、20-200uL、200-1000uL 3, 37℃ Incubator 4, Distilled water or deionized water 2. Sample processing and requirements: The detection range of the kit is not equivalent to the concentration range of the test substance in the sample It is recommended to estimate the concentration of the test substance in the sample through relevant literature before the experiment and determine the actual concentration of the sample through pre-experiment. If the concentration of the test substance in the sample is too high or too low, please dilute or concentrate the sample appropriately. If the sample tested is not among the sample types listed in the instructions, it is recommended to conduct pre-experiments to verify its detection effectiveness. Serum: Whole blood samples collected in serum separation tubes were placed at room temperature 2 Hour or 2-8℃ Overnight, then 1000×g Centrifugation 20 Minutes, take the supernatant, or place the supernatant in -20℃ Or -80℃ Store, but repeated freezing and thawing should be avoided. Plasma: use EDTA Or heparin as an anticoagulant to collect a sample, and collect the sample after collection 30 Within minutes 2-8℃1000×g Centrifugation 15 Minutes, take the supernatant to detect, or place the supernatant in -20℃ Or -80℃ Store, but repeated freezing and thawing should be avoided. Tissue homogenate: With pre-cooled PBS(0.01M,pH=7.4) The tissue is flushed to remove residual blood (lysed red blood cells in the homogenate can affect the test results), and the tissue is weighed and cut into pieces. Combining the shredded tissue with the corresponding volume PBS (Generally according to 1:9 Weight to volume ratio, such as 1g The tissue samples correspond to 9mL Of PBS The specific volume can be appropriately adjusted according to the experimental needs and recorded. Recommended in PBS Add protease inhibitor) into a glass homogenizer and grind thoroughly on ice or grind in a homogenizer. For further lysis of tissue cells, the homogenate can be sonicated, or freeze-thawed repeatedly. Finally, the homogenate was mixed in 5000×g Centrifugation 5~10 Minutes, take the supernatant for detection. Cell culture supernatant: Please 1000×g Centrifugation 20 Minutes, take the supernatant to detect, or place the supernatant in -20℃ Or -80℃ Store, but repeated freezing and thawing should be avoided. Cell lysate: Precooling for adherent cells PBS Gently washed, followed by trypsinization, 1000×g Centrifugation 5 Cells were collected after minutes. The suspended cells can be collected directly by centrifugation. The collected cells were pre-cooled with PBS Washing 3 Times, every 1×10^6 Added to cells 150-200μLPBS Resuspension (recommended at PBS Adding a protease inhibitor. If the content is very low, it can be appropriately reduced PBS Volume) and the cells were disrupted by repeated freeze-thaw or sonication. The extracts were mixed in 2-8℃, 1500×g Centrifugation 10 Minutes, take the supernatant for detection. Other biological samples: 1000×g Centrifugation 20 Minutes, take the supernatant to detect. Sample Appearance: The sample should be clear and transparent, and the suspended solids should be centrifuged to remove. Sample Preservation: After sample collection, if 1 Those tested within weeks can be stored in 4℃, if it cannot be detected in time, please pack it according to the one-time usage amount and freeze it in -20℃（1 Within months), or -80℃（6 Test within months) to avoid repeated freezing and thawing. Hemolysis of the sample will affect the final test result, so hemolyzed samples are not suitable for this test. 3. Sample dilution plan: Please estimate the concentration range of the sample in advance. If your test sample needs to be diluted, refer to the dilution plan as follows: Dilution 100 Times: One step dilution. Take 5μL Sample to 495μL Within universal diluent, do 100 Double dilution. Dilution 1000 Times: Two-step dilution. Take 5μL Sample to 95μL Within universal diluent, do 20 Dilute, and then take 5μL20 Double dilute sample to 245μL Within universal diluent, do 50 Double dilution, total dilution 1000 Times. Dilution 100000 Times: Three-step dilution. Take 5μL Sample to 195μL Within universal diluent, do 40 Dilute, and then take 5μL40 Double dilute sample to 245μL Within universal diluent, do 50 Time dilution, and finally take 5μL 2000 Double dilute sample to 245μL Within universal diluent, do 50 Double dilution, total dilution 100000 Times. The amount of liquid taken during each dilution step is not less than 3μL, the dilution factor is not more than 100 Times. Each step of dilution should be mixed evenly to avoid foaming. 4. Preparations before testing: 1, please advance 10 Minutes remove the kit from the refrigerator and equilibrate to room temperature. 2, Standard gradient working solution preparation: add 1mL Universal diluent into lyophilized standard and let stand 15 Minutes until it is completely dissolved and then gently mix (The concentration is 250ng/mL). And then according to the following concentrations: 250ng/mL、125ng/mL、62.5ng/mL、31.25ng/mL、15.62ng/mL、7.81ng/mL、3.9ng/mL、0ng/mL The dilution was performed. Double dilution method: Take 7 branch EP Tubes, each tube is added 500μL Universal diluent,250ng/mL Pipette from the standard working solution 500μL To the first EP Mix evenly in a tube 125ng/mL. According to this step, suck and mix the standard working solution in turn. The last tube is directly used as a blank hole, so there is no need to suck liquid from the penultimate tube, as shown in the figure below. 3, Preparation of biotinylated antibody detection working solution: before use 15 Minutes will 100× Concentrated biotinylation detection 1000×g Centrifugation 1 Minutes, with a universal diluent 100× Concentrated biotinylated detection antibody diluted into 1× Working concentration (Example: 10μL concentrate +990μL Universal diluent), now available for use. 4, Preparation of enzyme conjugate working solution: before use 15 Minutes will 100× Concentrated enzyme conjugate in 1000×g Centrifugation 1 Minutes, with a universal diluent 100× The concentrated enzyme conjugate is diluted into 1× Working concentration (Example: 10μL Concentrate +990μL Universal diluent), now available for use. 5, 1× Wash liquid preparation: Take 10mL20× Wash liquid to 190mL In distilled water (the concentrated washing liquid taken out from the refrigerator may have crystals, which is a normal phenomenon. It can be placed at room temperature and prepared after the crystals are completely dissolved). 5. Operation steps: 1, Equilibration from room temperature 10 After minutes, remove the required slats from the aluminum foil bag, and seal the remaining slats with ziplock bag and put them back 4℃. 2, Adding samples: respectively add samples or different concentration standards according to 100μL Each well is added to the corresponding well, and the blank well is added 100μL Universal diluent. After covering the sealing film 37℃ Incubation 60 Minutes. (Recommendation: minimum dilution of sample to be tested with universal diluent 1 Times later, add the enzyme labeled plate for testing. So as to reduce the influence of matrix effect on the test results, and finally, the sample concentration needs to be multiplied by the corresponding dilution factor when calculating. It is recommended to set up double wells for all samples and standards to be tested during testing). 3, Add biotinylated antibody detection: take out the enzyme labeled plate, discard the liquid, and do not wash it. Add directly to each well 100μL Biotinylated antibiotic detection working solution, after covering with sealing film 37℃ Incubation 60 Minutes. 4, Plate washing: discard the liquid and add to each well 300μL1x Wash liquid, stand 1 Minutes, throw off the washing liquid, pat dry on absorbent paper, and repeat washing the plate 3 Times (the plate can also be washed with a plate washing machine). 5, Add enzyme conjugate working solution: add each well 100μL Enzyme conjugate working solution, after covering with sealing membrane 37℃ Incubation 30 Minutes. 6, Plate washing: discard the liquid according to the steps 4 Washing method, wash plate 5 Times. 7, Add substrate: add per well 90μL Substrate (TMB) Covered with a sealing film, 37℃ Incubation protected from light 15 Minutes. 8, Add stop solution: take out the enzyme label plate and add it directly to each well 50μL Stop solution, immediately in 450nm Wavelength measurement of each well OD Value. VI. Calculation of experimental results: Result judgment: 1, calculate the average of the standard and sample replica well OD Value and subtract the blank hole's OD Values as correction values. Taking concentration as the abscissa, OD Value is ordinate, draw the standard curve of the four-parameter logic function on the double logarithmic coordinate paper. 2, If the sample OD If the value is higher than the upper limit of the standard curve, the test should be retested after appropriate dilution and multiplied by the corresponding dilution factor when calculating the sample concentration. 7. Kit performance: 1, Repeatability: the coefficient of variation in the plate is less than 10%, the interplate coefficient of variation is less than 10%. 2, Recovery rate: added to selected healthy serum, plasma and cell culture supernatant 3 Rats at different concentration levels TRAP, calculate the recovery. 3, linear dilution: respectively in the selected 4 Healthy serum, plasma and cell culture supernatant were added with high concentration of rats TRAP, linearity was assessed by dilution within the standard curve kinetic range. |
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| Sensitivity | 1.7ng/mL | |||||||||||||||||||||||||||||||||
| Species Reactivity | Rat | |||||||||||||||||||||||||||||||||
| Theory | This kit uses double antibody sandwich enzyme-linked immunosorbent assay (ELISA). Sample, standard, biotin-labeled detection antibody, HRP enzyme conjugate were sequentially added to microwells pre-coated with rat anti-tartrate acid phosphatase (TRAP) capture antibody, incubated and washed in the middle, and colored with substrate TMB. TMB was converted to blue under the catalysis of peroxidase (HRP) and to final yellow under the action of acid. There was a positive correlation between the depth of color and rat tartrate-resistant acid phosphatase (TRAP) in the sample. The absorbance (OD value) was measured with a microplate reader at a wavelength of 450nm, and the sample concentration was calculated. | |||||||||||||||||||||||||||||||||
| Synonym | Rat Acid Phosphatase 5, Tartrate Resistant (TRAP) ELISA Kit | |||||||||||||||||||||||||||||||||
| Detection Type | Double antibody sandwich method | |||||||||||||||||||||||||||||||||
| Composition |
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| Background | Tartrate-resistant acid phosphatase (TRAP), also called ACP5, is a glycosylated monomeric metalloproteinase expressed in mammals. It has a molecular weight of about 35kDa, has an alkaline isoelectric point (7.6-9.5) and is optimal for activity under acidic conditions. TRAP is synthesized as a latent proenzyme and activated by proteolysis and reduction. It is distinguished from other mammalian acid phosphatases by its resistance to tartrate inhibition and its molecular weight. | |||||||||||||||||||||||||||||||||
| Storage Temp. | Unopened kit, stored at 4 °C, shelf life 6 months. | |||||||||||||||||||||||||||||||||
| Test Range | 3.90-250ng/mL | |||||||||||||||||||||||||||||||||
| Applications | Serum, plasma, tissue homogenates and other biological fluids |
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4.5 ★★★★★
Based on 9 reviews
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Product Reviews
★★★★★ 4
Great Toy, but Big Dogs Destroy the Squeakers Fast
Color: Wild Duck, Hare, Squirrel & Alligator, Size: Large
My big dogs had the squeaker torn out in no time, but my little dog absolutely loves this toy. It’s the perfect size for her, and she carries it everywhere. Durable enough for small pups, just not tough enough for heavy chewers. Still a fun toy overall!
WAS THIS REVIEW HELPFUL?YesReportShare
Reviewed in the United States on February 15, 2026
★★★★★ 5
Fun for dogs
Color: Green/Alligator, Size: Small
Smaller than I expected, but the two little dogs love it!
They love shaking it, making it squeak, tugging it against each other & chasing it when I throw it to fetch. They often sleep laying on it.
WAS THIS REVIEW HELPFUL?YesReportShare
Reviewed in the United States on May 25, 2026
★★★★★ 3
WEIRD feature - requires a water bottle
Color: Cow, Size: Large
Cute, but buyer beware. Maybe the description said this, but who would think to read for this.... You have to insert an empty bottle (like an old water bottle) for it to make the crinkle noise. There is a velcro spot at the base where you can open it and insert the water bottle for the noise factor and your dogs entertainment. I've yet to do that, but feel like my dog is gonna figure out the velcro and get the bottle out in no time. Seems like a waste of money. I could just give her an empty water bottle without the toy for free.
WAS THIS REVIEW HELPFUL?YesReportShare
Reviewed in the United States on June 9, 2026
★★★★★ 5
Best dog toy!
Color: Multicolor/Alligator & Wild Duck, Size: Medium, Color: Multicolor/Alligator & Wild Duck, Size: Medium
Best dog toy! Most dog toys lady maybe a week or less but this one has been going strong for almost 2 months. Both the squeekers still work on both toys i purchased. My vizsla loves ti squeek and carry it around. We added an empty water bottle in the pocket cavity for some extra fun! Yes, we are still on the same water bottle! Fantastic durability.
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Reviewed in the United States on May 26, 2026
★★★★★ 3
Shows wear quickly
Color: Multicolor/Sheep & Cow, Size: Medium
These are cute but not holding up as well as I had hoped. Quality is ok and the Velcro has held up great. The fabric just isn’t as good as it could be. They are much larger than expected.
WAS THIS REVIEW HELPFUL?YesReportShare
Reviewed in the United States on April 28, 2026
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