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大鼠肿瘤坏死因子α(TNF-α)ELISA试剂盒Rat TNF-α ELISA kit
面议大鼠脂蛋白磷脂酶A2(Lp-PLA2)大鼠脂蛋白磷脂酶A2
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面议大鼠转化生长因子β1(TGF-β1)ELISA试剂盒 TGF-β1 ELISA试剂盒
面议大鼠转化生长因子α(TGF-α)ELISA试剂盒 转化生长因子α ELISA试剂盒
面议大鼠昼夜节律蛋白同源物2(PER2)ELISA试剂盒 PER2 ELISA试剂盒
面议大鼠周脂素(Plin1/Peri/Plin)ELISA试剂盒 周脂素 ELISA试剂盒
面议大鼠周期素依赖性激酶5(CDK5)ELISA试剂盒 CDK5 ELISA试剂盒
面议大鼠肿瘤特异生长因子/肿瘤相关因子(TSGF)ELISA试剂盒 TSGF ELISA试剂盒
面议大鼠肿瘤坏死因子诱导蛋白6(TSG-6)ELISA试剂盒 TSG-6 ELISA试剂盒
面议大鼠肿瘤坏死因子相关凋亡诱导配体(TRAIL)ELISA试剂盒 TRAIL ELISA试剂盒
面议大鼠肿瘤坏死因子受体超家族成员5(CD40)ELISA试剂盒 CD40 ELISA试剂盒
面议人肿瘤坏死因子α(TNF-α)人肿瘤坏死因子α ELISA试剂盒
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ELISA Kit
DADB-70P7.1, DIF, TNF-alpha, TNFA, TNFSF2, APC1 protein|TNF superfamily, member 2|TNF, macrophage-derived|TNF, monocyte-derived|cachectin|tumor necrosis factor alpha
96T
Human
Bovine Dog Goat Guinea pig Horse Mouse Rabbit Sheep Pig Chicken Fish Monkey Rat Human Hamster
tumor necrosis factor (TNF superfamily, member 2)
TNF
7.8 pg/ml-500 pg/ml
1.95 pg/ml
1-5h
50-100ul
450 nm
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This assay has high sensitivity and excellent specificity for detection of Human TNF. No significant cross-reactivity or interference between Human TNF and analogues was observed.
Intra-assay Precision (Precision within an assay): CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess.
Inter-assay Precision (Precision between assays): CV%<10%
Three samples of known concentration were tested in twenty assays to assess.
Serum: Use a serum separator tube (SST) and allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 15 minutes at 1000 ×g. Remove serum and assay immediat......+
Serum: Use a serum separator tube (SST) and allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 15 minutes at 1000 ×g. Remove serum and assay immediay or aliquot and store samples at -20°C or -80°C. Avoid repeated freeze-thaw cycles.
Plasma: Collect plasma using EDTA, or heparin as an anticoagulant. Centrifuge for 15 minutes at 1000 ×g at 2-8°C within 30 minutes of collection. Assay immediay or aliquot and store samples at -20°C or -80°C. Avoid repeated freeze-thaw cycles. ―
Bring all reagents and samples to room temperature before use. Centrifuge the sample again after thawing before the assay. It is recommended that all samples and standards be assayed in duplicate. 1......+
Bring all reagents and samples to room temperature before use. Centrifuge the sample again after thawing before the assay. It is recommended that all samples and standards be assayed in duplicate.
1. Prepare all reagents, working standards, and samples as directed in the previous sections.
2. Refer to the Assay Layout Sheet to determine the number of wells to be used and put any remaining wells and the desiccant back into the pouch and seal the ziploc, store unused wells at 4°C.
3. Add 100μl of standard and sample per well. Cover with the adhesive strip provided. Incubate for 2 hours at 37°C. A plate layout is provided to record standards and samples assayed.
4. Remove the liquid of each well, don't wash.
5. Add 100μl of Biotin-antibody (1x) to each well. Cover with a new adhesive strip. Incubate for 1 hour at 37°C. (Biotin-antibody (1x) may appear cloudy. Warm up to room temperature and mix gently until solution appears uniform.)
6. Aspirate each well and wash, repeating the process two times for a total of three washes. Wash by filling each well with Wash Buffer (200μl) using a squirt bottle, multi-channel pipette, manifold dispenser, or autowasher, and let it stand for 2 minutes, complete removal of liquid at each step is essential to good performance. After the last wash, remove any remaining wash Buffer by aspirating ordecanting. Invert the plate and blot it against clean paper towels.
7. Add 100μl of HRP-avidin (1x) to each well. Cover the microtiter plate with a new adhesive strip. Incubate for 1 hour at 37°C.
8. Repeat the aspiration/wash process for five times as in step 6.
9. Add 90μl of TMB Substrate to each well. Incubate for 15-30 minutes at 37°C. Protect from light.
10. Add 50μl of Stop Solution to each well, gently tap the plate to ensure thorough mixing.
11. Determine the optical density of each well within 5 minutes, using a microplate reader set to 450 nm. If wavelength correction is available, set to 540 nm or 570 nm. Subtract readings at 540 nm or 570 nm from the readings at 450 nm. This subtraction will correct for optical imperfections in the plate. Readings made directly at 450 nm without correction may be higher and less accurate.―
Using the professional soft "Curve Expert 1.3" to make a standard curve is recommended, which can be downloaded from our web. Average the duplicate readings for each standard and sample and subtract......+
Using the professional soft "Curve Expert 1.3" to make a standard curve is recommended, which can be downloaded from our web.
Average the duplicate readings for each standard and sample and subtract the average zero standard optical density.
Create a standard curve by reducing the data using computer software capable of generating a four parameter logistic (4-PL) curve-fit. As an alternative, construct a standard curve by plotting the mean absorbance for each standard on the x-axis against the concentration on the y-axis and draw a best fit curve through the points on the graph. The data may be linearized by plotting the log of the TNF concentrations versus the log of the O.D. and the best fit line can be determined by regression analysis. This procedure will produce an adequate but less precise fit of the data.
If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.―
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The Peritoneal Leptin, MCP
Product-specific
3.05
American Journal of Reproductive Immunology