TNNC1 ELISA 试剂盒
TNNC1
适用: 小鼠
Colorimetric
Sandwich ELISA
Serum
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- 抗原 See all TNNC1 ELISA试剂盒
- TNNC1 (Cardiac Troponin C (TNNC1))
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适用
- 小鼠
- 检测方法
- Colorimetric
- 实验类型
- Sandwich ELISA
- 应用范围
- ELISA
- 样品类型
- Serum
- Analytical Method
- Quantitative
- 组件
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Anti-cTnI-coated microtiter wells, 96 wells
Mouse cTnI Calibrator (lyophilized), reconstitute with 0.40 mL H2O
cTnI Calibrator Diluent, 12 mL
cTnI HRP Conjugate, 11 mL
Wash Solution (20X), 50 mL
TMB Reagent (HRP substrate solution), 11 mL
Stop Solution (1N HCl), 11 mL. - 试剂未包括
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Pipettes: P-10, P-200 & P-1000 or equivalent
Disposable pipette tips
Distilled or de-ionized water
Vortex mixer
Absorbent paper
Graph paper or appropriate PC graphing software
Polypropylene microcentrifuge tubes (1.5 mL)
Microtiter plate reader capable of reading 0 to 4 OD at 450 nm. - Featured
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- 板类型
- Pre-coated
- 实验流程
- The high sensitivity Mouse Cardiac Troponin-I ELISA recognizes an epitope on mouse cTnI that is relatively resistant to proteolysis in mouse serum, thereby improving detection capability. The assay uses two different affinity purified antibodies. One is used for solid phase immobilization (on the microtiter wells). The second is conjugated to horseradish peroxidase (HRP). The serum sample is allowed to react simultaneously with the two antibodies, resulting in cTnI being sandwiched between the solid phase and HRP-conjugated antibodies. After one hour incubation at room temperature on a plate shaker, the wells are washed to remove unbound HRP-conjugated antibodies. A solution of TMB (Tetramethylbenzidine), an HRP substrate, is then added and incubated for 20 minutes, resulting in the development of a blue color. The color development is stopped with the addition of 1N HCl changing the color to yellow. The concentration of cTnI is proportional to the absorbance at 450 nm.
- 样品制备
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Serum should be prepared as quickly as possible after blood collection and stored at 4°C. All samples should be similarly processed (i.e., storage times and temperatures should be the same). If serum samples cannot be assayed immediately they should be frozen at -70°C and thawed only once prior to use.
- 实验流程
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- Secure the desired number of coated wells in the holder.
2. Dispense 100 µL of cTnI HRP Conjugate into each well.
3. Dispense 100 µL of calibrators and samples into the appropriate wells.
4. Thoroughly mix for 10-15 seconds. It is very important to mix completely.
5. Incubate at room temperature (18-25°C) on a plate shaker (150 rpm) for one hour.
6. Remove the incubation mixture either with a plate washer or by flicking plate contents into a bio-waste container.
7. Wash and empty the microtiter wells 5 times with 1X wash solution. This may be performed using either a plate washer (400 µL/well) or with a squirt bottle. The entire wash procedure should be performed as quickly as possible
8. Strike the wells sharply onto adsorbent paper or paper towels to remove all residual droplets.
9. Dispense 100 µL of TMB Reagent solution into each well. Gently mix for 5 seconds.
10. Incubate on a plate shaker (150 rpm) at room temperature for 20 minutes.
11. Stop the reaction by adding 100 µL of Stop Solution to each well.
12. Gently mix until all the blue color changes to yellow.
13. Read absorbance at 450 nm with a microtiter plate reader within 15 minutes. Please note: Due to plate reader differences, the high calibrator absorbance values may be out of range occasionally. If this occurs, absorbance values may be determined at 405 nm instead.
14. If absorbance values exceed the high calibrator, the samples should be appropriately diluted with sample diluent and re-determined. Samples with absorbance values below those of the lowest calibrator should be assigned a zero troponin-I value.
- Secure the desired number of coated wells in the holder.
- 结果分析
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- Calculate the mean absorbance values (A450) for each set of reference calibrators and samples.
2. Construct a calibration curve by plotting the mean absorbance obtained from each reference calibrator against its concentration in ng/mL on graph paper, with absorbance values on the vertical or Y-axis and concentration on the horizontal or X-axis.
3. Using the mean absorbance value for each sample, determine the corresponding concentration of cTnI in ng/mL from the calibration curve.
4. If available, graphing software may be used to analyze the data. Depending on the range of the calibration curve used, we find that good fits of the data may be obtained with linear regression analysis or using a two-site binding model. Alternatively, calibration curves may be generated using a point-to-point fit.
- Calculate the mean absorbance values (A450) for each set of reference calibrators and samples.
- 限制
- 仅限研究用
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- 储存条件
- 4 °C/-20 °C
- 储存方法
- The lyophilized reference calibrator should be stored at -20°C for optimum stability. The remainder of the kit should be stored refrigerated at 4°C. Keep the microtiter plate in a sealed bag with desiccant to minimize exposure to damp air. The expiration date of the kit is indicated on the box label.
- 有效期
- The expiry date is stated on the label.
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- 抗原 See all TNNC1 ELISA试剂盒
- TNNC1 (Cardiac Troponin C (TNNC1))
- 别名
- Cardiac Troponin-1 (TNNC1 产品)
- 别名
- CMD1Z ELISA Kit, CMH13 ELISA Kit, TN-C ELISA Kit, TNC ELISA Kit, TNNC ELISA Kit, cTnC ELISA Kit, tnnc1 ELISA Kit, zgc:103465 ELISA Kit, PCTNC1 ELISA Kit, cmd1z ELISA Kit, cmh13 ELISA Kit, tnc ELISA Kit, tnnc ELISA Kit, MGC80066 ELISA Kit, TNNC1 ELISA Kit, AI874626 ELISA Kit, TnC ELISA Kit, cTnI ELISA Kit, tncc ELISA Kit, Tncc ELISA Kit, stnnc ELISA Kit, zgc:86932 ELISA Kit, troponin C1, slow skeletal and cardiac type ELISA Kit, troponin C type 1a (slow) ELISA Kit, troponin C type 1 (slow) L homeolog ELISA Kit, cardiac troponin C ELISA Kit, troponin C, cardiac/slow skeletal ELISA Kit, troponin C type 1b (slow) ELISA Kit, TNNC1 ELISA Kit, tnnc1a ELISA Kit, tnnc1.L ELISA Kit, tnnc1 ELISA Kit, Tnnc1 ELISA Kit, tnnc1b ELISA Kit
- 背景
- Troponin is the inhibitory or contractile regulating protein complex of striated muscle. It is located periodically along the thin filament of the muscle and consists of three distinct proteins: troponin I, troponin C, and troponin T. The troponin I subunit exists in three isoforms, two in fast-twitch and slow-twitch skeletal muscle fibers, and one in cardiac muscle. At the sequence level cardiac troponin-I (cTnI) is significantly different from the skeletal isoforms and antibodies can be prepared that specifically recognize cTnI. The unique isoform and tissue specificity of cTnI are the basis for its use as a marker of cardiac muscle damage.
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