TNNC1 Kit ELISA

N° du produit ABIN956141

Détail du produit TNNC1 Kit ELISA

Antigène: TNNC1 (Cardiac Troponin C (TNNC1))

Reactivité: Singe

Méthode de détection: Colorimetric

Type de méthode: Sandwich ELISA

Application: ELISA

Type d'échantillon: Serum

Analytical Method: Quantitative

Ingrédients: Anti-cTnI-coated microtiter wells, 96 wells
Monkey cTnI Calibrator (lyophilized), reconstitute with 0.40 mL H2O
cTnI 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.

Matériel non inclus: 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.

Information d'application

Plaque: Pre-coated

Protocole: The Monkey Cardiac Troponin-I ELISA uses two different affinity purified cTnI specific 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.

Préparation de l'échantillon:

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.

Procédure de l'essai:

1. 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. Incubate at room temperature (18-25°C) on a plate shaker (150 rpm) for one hour.
   5. Remove the incubation mixture either with a plate washer or by flicking plate contents into a bio-waste container.
   6. 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 (use of a plate washer gives optimal results).
   7. Strike the wells sharply onto adsorbent paper or paper towels to remove all residual droplets.
   8. Dispense 100 µL of TMB Reagent solution into each well. Gently mix for 5 seconds.
   9. Incubate on a plate shaker (150 rpm) at room temperature for 20 minutes.
   10. Stop the reaction by adding 100 µL of Stop Solution to each well.
   11. Gently mix until all the blue color changes to yellow.
   12. 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.
   13. If absorbance values exceed the high calibrator, the samples should be appropriately diluted with cTnI diluent and re-determined. Samples with absorbance values below those of the lowest calibrator should be assigned a zero troponin-I value.

Calcul des résultats:

1. 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.

Restrictions: For Research Use only

Stockage

Stock: 4 °C/-20 °C

Stockage commentaire: 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.

Date de péremption: The expiry date is stated on the label.

Détail du antigène

Antigène: TNNC1 (Cardiac Troponin C (TNNC1))

Autre désignation: Cardiac Troponin-1 (TNNC1 Produits)

Synonymes: CMD1Z Kit ELISA, CMH13 Kit ELISA, TN-C Kit ELISA, TNC Kit ELISA, TNNC Kit ELISA, cTnC Kit ELISA, tnnc1 Kit ELISA, zgc:103465 Kit ELISA, PCTNC1 Kit ELISA, cmd1z Kit ELISA, cmh13 Kit ELISA, tnc Kit ELISA, tnnc Kit ELISA, MGC80066 Kit ELISA, TNNC1 Kit ELISA, AI874626 Kit ELISA, TnC Kit ELISA, cTnI Kit ELISA, tncc Kit ELISA, Tncc Kit ELISA, stnnc Kit ELISA, zgc:86932 Kit ELISA, troponin C1, slow skeletal and cardiac type Kit ELISA, troponin C type 1a (slow) Kit ELISA, troponin C type 1 (slow) L homeolog Kit ELISA, cardiac troponin C Kit ELISA, troponin C, cardiac/slow skeletal Kit ELISA, troponin C type 1b (slow) Kit ELISA, TNNC1 Kit ELISA, tnnc1a Kit ELISA, tnnc1.L Kit ELISA, tnnc1 Kit ELISA, Tnnc1 Kit ELISA, tnnc1b Kit ELISA

Sujet: 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.