NKA Kit ELISA

N° du produit ABIN1979203

Détail du produit NKA Kit ELISA

Antigène: NKA (Neurokinin A)

Reactivité: Humain, Souris, Rat

Méthode de détection: Colorimetric

Type de méthode: Competition ELISA

Gamme de detection: 0.1-1.000 pg/mL

Seuil minimal de détection: 0.1 pg/mL

Application: ELISA

Fonction: Human/Mouse/Rat Neurokinin-A EIA Kit optimized for serum and cell culture medium. Competition-based ELISA on a 96-well strip plate.

Type d'échantillon: Cell Culture Supernatant, Serum

Analytical Method: Quantitative

Specificité: Cross Reactivity: This EIA kit shows no cross-reactivity with any of the cytokines tested: Ghrelin, Nesfatin, Angiotensin II, NPY and APC.

Réactivité croisée (Details): This ELISA kit shows no cross-reactivity with any of the cytokines tested: Ghrelin, Nesfatin, Angiotensin II, NPY and APC.

Sensibilité: 0.8 pg/mL

Attributs du produit:

• Strip plates and additional reagents allow for use in multiple experiments
• Quantitative protein detection
• Establishes normal range
• The best products for confirmation of antibody array data

Ingrédients:

• Pre-Coated 96-well Strip Microplate
• Wash Buffer
• Standard Peptide
• Assay Diluent(s)
• Biotinylated Peptide
• HRP-Streptavidin
• TMB One-Step Substrate
• Stop Solution
• Assay Diagram
• Positive Control Sample
• Capture Antibody
• User Manual

Matériel non inclus:

• Distilled or deionized water
• Precision pipettes to deliver 2 μL to 1 mL volumes
• Adjustable 1-25 mL pipettes for reagent preparation
• 100 mL and 1 liter graduated cylinders
• Tubes to prepare standard and sample dilutions
• Orbital shaker
• Aluminum foil
• Saran Wrap
• Absorbent paper
• Microplate reader capable of measuring absorbance at 450nm
• SigmaPlot software (or other software that can perform four-parameter logistic regression models)

Information d'application

Indications d'application: Recommended Dilution for serum and plasma samplesHuman: 2X / Mouse: 2X / Rat: 2X

Volume d'échantillon: 100 μL

Durée du test: 5 h

Plaque: Pre-coated

Protocole:

1. Prepare all reagents, samples and standards as instructed.
2. Add 100 μL detection antibody to each well.
3. Incubate 1.5 h at RT or O/N at 4 °C.
4. Add 100 μL standard or sample to each well.
5. Incubate 2.5 h at RT.
6. Add 100 μL prepared streptavidin solution.
7. Incubate 45 min at RT.
8. Add 100 μL TMB One-Step Substrate Reagent to each well.
9. Incubate 30 min at RT.
10. Add 50 μL Stop Solution to each well.
11. Read plate at 450 nm immediately.

Préparation des réactifs:

1. Keep kit reagents on ice during steps. Equilibrate plate to room temperature before opening the sealed pouch.
   2. Assay Diluent B (Item E) should be diluted 5-fold with deionized or distilled water.
   3. Briefly centrifuge the Anti-Neurokinin A Antibody vial (Item N) before use. Add 50 µL of 1x Assay Diluent B into the vial to prepare a detection antibody concentrate. Pipette up and down to mix gently.
   4. The antibody concentrate should then be diluted 100-fold with 1x Assay Diluent B. This is your anti-Neurokinin A antibody working solution, which will be used in step 2 of the Assay Procedure. NOTE: the following steps may be done during the antibody incubation procedure (step 2 of Assay Procedure).
   5. Briefly centrifuge the vial of Biotinylated Neurokinin A (Item F) before use. Add 5 µL of Item F to 5 mL of the appropriate Assay Diluent. Pipette up and down to mix gently. The final concentration of biotinylated Neurokinin A will be 10 pg/mL. This solution will only be used as the diluent in step 6 of Reagent Preparation.
   6. Preparation of Standards: Label 6 microtubes with the following concentrations: 1000 pg/mL, 100 pg/mL, 10 pg/mL, 1 pg/mL, 0.1 pg/mL and 0 pg/mL. Pipette 450 mL of biotinylated Neurokinin A solution into each tube, except for the 1000 pg/mL (leave this one empty). It is very important to make sure the concentration of biotinylated Neurokinin A is 10 pg/mL in all standards. a. Briefly centrifuge the vial of Neurokinin A (Item C). In the tube labeled 1000 pg/mL, pipette 8 µL of Item C and 792 µL of 10 pg/mL biotinylated Neurokinin A solution (prepared in step 5 above). This is your Neurokinin A stock solution (1000 pg/mL Neurokinin A, 10 pg/mL biotinylated Neurokinin A). Mix thoroughly. This solution serves as the first standard. b. To make the 100 pg/mL standard, pipette 50 µL of Neurokinin A stock solution the tube labeled 100 pg/mL. Mix thoroughly. c. Repeat this step with each successive concentration, preparing a dilution series as shown in the illustration below. Each time, use 450 mL of biotinylated Neurokinin A and 50 mL of the prior concentration until 0.1 pg/mL is reached. Mix each tube thoroughly before the next transfer. d. The final tube (0 pg/mL Neurokinin A, 10 pg/mL biotinylated Neurokinin A) serves as the zero standard (or total binding).
   7. Prepare a 10-fold dilution of Item F. To do this, add 2 mL of Item F to 18 mL of the appropriate Assay Diluent. This solution will be used in steps 8 and
   10.
   8. Positive Control Preparation: briefly centrifuge the positive control vial (Item M). To the tube of Item M, add 101 µL 1x Assay Diluent B. Also add 2 µL of 10-fold diluted Item F (prepared in step 7) to the tube. This is a 2-fold dilution of the positive control. Mix thoroughly. The positive control is a cell culture medium sample that is meant to be a system control (to verify that the detection & kit components are working). It may be diluted further if desired, but be sure the final concentration of biotinylated Neurokinin A is 10 pg/mL.
   9. If Item B (20X Wash Concentrate) contains visible crystals, warm to room temperature and mix gently until dissolved. 1000 100 10 1 0.1 0 pg/mL pg/mL pg/mL pg/mL pg/mL pg/mL 50 mL 50 mL 50 mL 50 mL Dilute 20 mL of Wash Buffer Concentrate into deionized or distilled water to yield 400 mL of 1X Wash Buffer.
   10. Sample Preparation: Use Assay Diluent A + biotinylated Neurokinin A to dilute serum/plasma samples. For cell culture medium and other sample types, use 1X Assay Diluent B + biotinylated Neurokinin A as the diluent. It is very important to make sure the final concentration of the biotinylated Neurokinin A is 10 pg/mL in every sample.
   Example: to make a 4-fold dilution of sample, mix together 2.5 µL of 10-fold diluted Item F (prepared in step 7), 185 mL of appropriate Assay Diluent, and 62.5 µL of your sample, mix gently. The total volume is 250 µl, enough for duplicate wells on the microplate. Do not use Item F diluent from Step 5 for sample preparation. If you plan to use undiluted samples, you must still add biotinylated Neurokinin A to a final concentration of 10 pg/mL.
   Example: Add 2.5 mL of 10-fold diluted Item F to 247.5 mL of sample.
   11. Briefly centrifuge the HRP-Streptavidin vial (Item G) before use. The HRP-Streptavidin concentrate should be diluted 160- fold with 1X Assay Diluent B. Note: Do not use Assay Diluent A for HRP-Streptavidin preparation in Step 11.

Préparation de l'échantillon:

Use Assay Diluent A + biotinylated Neurokinin A to dilute serum/plasma samples. For cell culture medium and other sample types, use 1X Assay Diluent B + biotinylated Neurokinin A as the diluent. It is very important to make sure the final concentration of the biotinylated Neurokinin A is 10 pg/mL in every sample. EXAMPLE: to make a 4-fold dilution of sample, mix together 2.5 µL of 10-fold diluted Item F (prepared in step 7), 185 mL of appropriate Assay Diluent, and 62.5 µL of your sample, mix gently. The total volume is 250 µl, enough for duplicate wells on the microplate. Do not use Item F diluent from Step 5 for sample preparation. If you plan to use undiluted samples, you must still add biotinylated Neurokinin A to a final concentration of 10 pg/mL. EXAMPLE: Add 2.5 mL of 10-fold diluted Item F to 247.5 mL of sample.

Procédure de l'essai:

1. Keep kit reagents on ice during reagent preparation steps. It is recommended that all standards and samples be run at least in duplicate.
   2. Add 100 µL anti-Neurokinin A antibody (see Reagent Preparation step 4) to each well. Incubate for 1.5 hours at room temperature with gentle shaking (1-2 cycles/sec). You may also incubate overnight at 4 degrees C.
   3. Discard the solution and wash wells 4 times with 1x Wash Buffer (200-300 µL each), Washing may be done with a multichannel pipette or an automated plate washer. Complete removal of liquid at each step is essential to good assay performance. After the last wash, remove any remaining Wash Buffer by aspirating or decanting. Invert the plate and blot it against clean paper towels.
   4. Add 100 µL of each standard (see Reagent Preparation step 6), positive control (see Reagent Preparation step 8) and sample (see Reagent Preparation step 10) into appropriate wells. Be sure to include a blank well (Assay Diluent only). Cover wells and incubate for 2.5 hours at room temperature with gentle shaking (1-2 cycles/sec) or overnight at 4 °C.
   5. Discard the solution and wash 4 times as directed in Step
   3.
   6. Add 100 µL of prepared HRP-Streptavidin solution (see Reagent Preparation step 11) to each well. Incubate for 45 minutes with gentle shaking at room temperature. It is recommended that incubation time should not be shorter or longer than 45 minutes.
   7. Discard the solution and wash 4 times as directed in Step
   3.
   8. Add 100 µL of TMB One-Step Substrate Reagent (Item H) to each well. Incubate for 30 minutes at room temperature in the dark with gentle shaking (1-2 cycles/sec).
   9. Add 50 µL of Stop Solution (Item I) to each well. Read absorbances at 450 nm immediately. 1

Calcul des résultats:

Calculate the mean absorbance for each set of duplicate standards, controls and samples, and subtract the blank optical density. Plot the standard curve using SigmaPlot software (or other software which can perform four-parameter logistic regression models), with standard concentration on the x-axis and percentage of absorbance on the y-axis. Draw the best-fit curve through the standard points.

Précision du teste: Intra-Assay: CV < 10 %
Inter-Assay: CV < 15 %

Restrictions: For Research Use only

Stockage

Conseil sur la manipulation: Avoid repeated freeze/thaw cycles.

Stock: -20 °C

Stockage commentaire: Standard, Biotinylated Neurokinin A peptide, and Positive Control should be stored at -20°C after arrival. Avoid multiple freeze-thaws. The remaining kit components may be stored at 4°C. Opened Microplate Wells and antibody (Item N) may be stored for up to 1 month at 2° to 8°C. Return unused wells to the pouch containing desiccant pack and reseal along entire edge.

Date de péremption: 6 months

Références pour NKA Kit ELISA (ABIN1979203)

Słoniecka, Le Roux, Boman, Byström, Zhou, Danielson: "Expression Profiles of Neuropeptides, Neurotransmitters, and Their Receptors in Human Keratocytes In Vitro and In Situ." dans: PLoS ONE, Vol. 10, Issue 7, pp. e0134157, (2015) (PubMed).

Dornan, Vink, Malen, Short, Struthers, Barrett: "Site-specific effects of intracerebral injections of three neurokinins (neurokinin A, neurokinin K, and neurokinin gamma) on the expression of male rat sexual behavior." dans: Physiology & behavior, Vol. 54, Issue 2, pp. 249-58, (1993) (PubMed).

Carter, Krause: "Structure, expression, and some regulatory mechanisms of the rat preprotachykinin gene encoding substance P, neurokinin A, neuropeptide K, and neuropeptide gamma." dans: The Journal of neuroscience : the official journal of the Society for Neuroscience, Vol. 10, Issue 7, pp. 2203-14, (1990) (PubMed).

Détail du antigène

Antigène: NKA (Neurokinin A)

Abstract: NKA Produits

Synonymes: Hs.2563 Kit ELISA, NK2 Kit ELISA, NKNA Kit ELISA, NPK Kit ELISA, TAC2 Kit ELISA, PPTA3 Kit ELISA, Ppt5fl Kit ELISA, RATPPTA3 Kit ELISA, TAC Kit ELISA, 4930528L02Rik Kit ELISA, NK-1 Kit ELISA, NK1 Kit ELISA, Nkna Kit ELISA, PPT-A Kit ELISA, PPTA Kit ELISA, SP Kit ELISA, tachykinin precursor 1 Kit ELISA, tachykinin, precursor 1 Kit ELISA, tachykinin 1 Kit ELISA, TAC1 Kit ELISA, Tac1 Kit ELISA

Sujet: Neurokinin A (NKNA)

ID gène: 6863

UniProt: P20366