Thymic Stromal Lymphopoietin Kit ELISA
Aperçu rapide pour Thymic Stromal Lymphopoietin Kit ELISA (ABIN8056665)
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Méthode de détection
Type de méthode
Gamme de detection
Application
Type d'échantillon
Classe de qualité
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Seuil minimal de détection
- 7.8 pg/mL
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Fonction
- The kit is a high sensitivity sandwich enzyme immunoassay for in vitro quantitative measurement of TSLP in human serum, plasma, tissue homogenates, cell lysates, cell culture supernates.
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Analytical Method
- Quantitative
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Specificité
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This assay has high sensitivity and excellent specificity for detection of High Sensitive Thymic Stromal Lymphopoietin (TSLP).
No significant cross-reactivity or interference between High Sensitive Thymic Stromal Lymphopoietin (TSLP) and analogues was observed. -
Sensibilité
- < 3.1 pg/mL
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Ingrédients
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- Pre-coated, 96-well strip plate
- Plate sealer
- Standard
- Standard Diluent
- Detection Reagent A
- Assay Diluent A
- Detection Reagent B
- Assay Diluent B
- TMB Substrate
- Stop Solution
- Wash Buffer (30X)
- Instruction manual
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Matériel non inclus
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- Microplate reader with 450 ± 10nm filter.
- Precision single or multi-channel pipettes and disposable tips.
- Eppendorf Tubes for diluting samples.
- Deionized or distilled water.
- Absorbent paper for blotting the microtiter plate.
- Container for Wash Solution
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Volume d'échantillon
- 100 μL
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Durée du test
- 3 h
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Plaque
- Pre-coated
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Protocole
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1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 2 hours at 37°C;
3. Aspirate and add 100µL prepared Detection Reagent A. Incubate 1 hour at 37°C;
4. Aspirate and wash 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
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Préparation des réactifs
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- Bring all kit components and samples to room temperature (18-25°C) before use. If the kit will not be used up in one time, please only take out strips and reagents for present experiment, and leave the remaining strips and reagents in required condition.
- Standard - Reconstitute the Standard with 1.0 mL of Standard Diluent, kept for 10 minutes at room temperature, shake gently(not to foam). The concentration of the standard in the stock solution is 1,000pg/mL. Please firstly dilute the stock solution to 500pg/mL and the diluted standard serves as the highest standard (500pg/mL). Then prepare 7 tubes containing 0.5 mL Standard Diluent and use the diluted standard to produce a double dilution series according to the picture shown below. Mix each tube thoroughly before the next transfer. Set up 7 points of diluted standard such as 500pg/mL, 250pg/mL, 125pg/mL, 62.5pg/mL, 31.2pg/mL, 15.6pg/mL, 7.8pg/mL, and the last EP tubes with Standard Diluent is the blank as 0pg/mL.
- Detection Reagent A and Detection Reagent B - Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute them to the working concentration 100-fold with Assay Diluent A and B, respectively.
- Wash Solution - Dilute 20 mL of Wash Solution concentrate (30x) with 580 mL of deionized or distilled water to prepare 600 mL of Wash Solution (1x).
- TMB substrate - Aspirate the needed dosage of the solution with sterilized tips and do not dump the residual solution into the vial again.
Note:
- Making serial dilution in the wells directly is not permitted.
- Prepare standards within 15 minutes before assay. Please do not dissolve the reagents at 37°C directly.
- Please carefully reconstitute Standards or working Detection Reagent A and B according to the instruction, and avoid foaming and mix gently until the crystals are completely dissolved. To minimize imprecision caused by pipetting, use small volumes and ensure that pipettors are calibrated. It is recommended to suck more than 10μL for one pipetting.
- The reconstituted Standards, Detection Reagent A and Detection Reagent B can be used only once.
- If crystals have formed in the Wash Solution concentrate (30x), warm to room temperature and mix gently until the crystals are completely dissolved.
- Contaminated water or container for reagent preparation will influence the detection result.
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Restrictions
- For Research Use only
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Conseil sur la manipulation
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The stability of kit is determined by the loss rate of activity. The loss rate of this kit is less than 5% within the expiration date under appropriate storage condition.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end. -
Stock
- 4 °C,-20 °C
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Stockage commentaire
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- For unopened kit: All the reagents should be kept according to the labels on vials. The Standard, Detection Reagent A, Detection Reagent B and the 96-well strip plate should be stored at -20°C upon receipt while the others should be at 4°C.
- For opened kit: When the kit is opened, the remaining reagents still need to be stored according to the above storage condition. Besides, please return the unused wells to the foil pouch containing the desiccant pack, and reseal along entire edge of zip-seal.
Note: It is highly recommended to use the remaining reagents within 1 month provided this is within the expiration date of the kit. - For ELISA kit, 1 day storage at 37°C can be considered as 2 months at 4°C, which means 3 days at 37°C equaling 6 months at 4°C.
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Date de péremption
- 6 months
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- Thymic Stromal Lymphopoietin (TSLP)
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Autre désignation
- Thymic Stromal Lymphopoietin
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UniProt
- Q969D9
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