Thyroid Stimulating Hormone (TSH) ELISA Kit

Details zu Produkt Nr. ABIN3159158, Anbieter: Anmelden zum Anzeigen
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Reaktivität
Maus
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Methodentyp
Competition ELISA
Detektionsbereich
49.4-4000 pg/mL
Untere Nachweisgrenze
49.4 pg/mL
Applikation
ELISA
Optionen
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'Independent Validation' Siegel
Antigen mTSH
Chargennummer L170428173
Validierte Anwendung ELISA
Positivkontrolle

euthyroid mouse serum

low (50pg/ml), medium (250pg/ml), and high (2500pg/ml) mTSH concentration reference standards (Cloud Clone) undiluted or diluted 1:2 in Standard Diluent

Negativkontrolle

Blank samples Standard Diluent only

Bewertung

Passed, the murine TSH ELISA kit ABIN415519 specifically detects the antigen in euthyroid mouse serum.

Protokoll
  • Bring all reagents and samples to room temperature before use.
  • Prepare the standards as described in the kit manual. It is very important to allow the stock to sit for 10min and the prepared standards for 15min at RT.
  • Pipette 50µl of the diluted kits standard, blank, and the sample to each well diluted as indicated above.
  • Add immediately 50µl Detection Reagent A diluted 1:100in Assay Diluent A to each well.
  • Seal plate with an adhesive strip and mix the plate gently and let it incubate for 1h at 37°C.
  • Remove the solution and wash the wells 4x for 1min with 350µl Wash Solution diluted to 1x in distilled H2O.
  • After the last washing step, remove the remaining liquid by inverting and blotting the plate against absorbent paper.
  • Add 100µl Detection Reagent B diluted 1:100 in Assay Diluent B to each well.
  • Seal plate with an adhesive strip and let the plate incubate for 30min at 37°C.
  • Remove the solution and wash 5x for 1min 350µl Wash Solution diluted to 1x in distilled H2O.
  • Add 90µl TMB Substrate.
  • Seal plate with an adhesive strip and incubate the plate for 15min at 37°C.
  • Add 50µl Stop Solution, mix the plate gently and measure immediately the absorbance at 450nm.
Anmerkungen
  • The Assay is very sensitive. Therefore it is very important to check all reagents before use. Do not use any reagents that appear cloudy.
  • In addition to that it is necessary to store the kit under the recommended conditions. If the entire kit is used at once, it is necessary aliquot the reagents and take out only the strips for the present assay.
  • All diluted reagents have to be mixed very gently.
Validierungsbilder
ELISA validation image for Thyroid Stimulating Hormone (TSH) ELISA Kit (ABIN415519)

A. Standard curve for ABIN415519, generated from one measurement of the absorbance...

Verwendungszweck The kit is a competitive inhibition enzyme immunoassay technique for the in vitro quantitative measurement of TSH in Serum,Plasma,Biological Fluids
Proben Serum, Plasma, Biological Fluids
Analytische Methode Quantitative
Nachweismethode Colorimetric
Spezifität

This assay has high sensitivity and excellent specificity for detection of Thyroid Stimulating Hormone (TSH).
No significant cross-reactivity or interference between Thyroid Stimulating Hormone (TSH) and analogues was observed.

Kreuzreaktivität (Details) No significant cross-reactivity or interference between Thyroid Stimulating Hormone (TSH) and analogues was observed.
Sensitivität 19.2 pg/mL
Bestandteile
  • Pre-coated, ready to use 96-well strip plate
  • Plate sealer for 96 wells
  • Standard Diluent
  • Assay Diluent A
  • Assay Diluent B
  • Stop Solution
  • Standard
  • Detection Reagent A
  • Detection Reagent B
  • TMB Substrate
  • Wash Buffer (30 × concentrate)
  • Instruction manual
Benötigtes Material
  • Microplate reader with 450 nm 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
Andere Bezeichnung TSH
Forschungsgebiet Hormones, Cancer, Endocrine system
Applikationshinweise
  • Limited by the current condition and scientific technology, we cannot completely conduct the comprehensive identification and analysis on the raw material provided by suppliers. So there might be some qualitative and technical risks to use the kit.
  • The final experimental results will be closely related to validity of the products, operation skills of the end users and the experimental environments. Please make sure that sufficient samples are available.
  • Kits from different batches may be a little different in detection range, sensitivity and color developing time.
  • Do not mix or substitute reagents from one kit lot to another. Use only the reagents supplied by manufacturer.
  • Protect all reagents from strong light during storage and incubation. All the bottle caps of reagents should be covered tightly to prevent the evaporation and contamination of microorganism.
  • There may be some foggy substance in the wells when the plate is opened at the first time. It will not have any effect on the final assay results. Do not remove microtiter plate from the storage bag until needed.
  • Wrong operations during the reagents preparation and loading, as well as incorrect parameter setting for the plate reader may lead to incorrect results. A microplate plate reader with a bandwidth of 10nm or less and an optical density range of 0-3 O.D. or greater at 450 ± 10nm wavelength is acceptable for use in absorbance measurement. Please read the instruction carefully and adjust the instrument prior to the experiment.
  • Even the same operator might get different results in two separate experiments. In order to get better reproducible results, the operation of every step in the assay should be controlled. Furthermore, a preliminary experiment before assay for each batch is recommended.
  • Each kit has been strictly passed Q.C test. However, results from end users might be inconsistent with our in-house data due to some unexpected transportation conditions or different lab equipments. Intra-assay variance among kits from different batches might arise from above factors, too.
  • Kits from different manufacturers for the same item might produce different results, since we have not compared our products with other manufacturers.
Kommentare

Information on standard material:
The standard might be recombinant protein or natural protein, that will depend on the specific kit. Moreover, the expression system is E.coli or yeast or mammal cell. There is 0.05% proclin 300 in the standard as preservative.

Information on reagents:
The stop solution used in the kit is sulfuric acid with concentration of 1 mol/L. And the wash solution is TBS. The standard diluent contains 0.02 % sodium azide, assay diluent A and assay diluent B contain 0.01% sodium azide. Some kits can contain is BSA in them.

Information on antibodies:
The provided antibodies and their host vary in different kits.

Probenmenge 50 μL
Testdauer 2 h
Plattentyp Pre-coated
Protokoll This assay employs the competitive inhibition enzyme immunoassay technique. A monoclonal antibody specific to Thyroid Stimulating Hormone (TSH) has been pre-coated onto a microplate. A competitive inhibition reaction is launched between biotin labeled Thyroid Stimulating Hormone (TSH) and unlabeled Thyroid Stimulating Hormone (TSH) (Standards or samples) with the pre-coated antibody specific to Thyroid Stimulating Hormone (TSH). After incubation the unbound conjugate is washed off. Next, avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. The amount of bound HRP conjugate is reverse proportional to the concentration of Thyroid Stimulating Hormone (TSH) in the sample. After addition of the substrate solution, the intensity of color developed is reverse proportional to the concentration of Thyroid Stimulating Hormone (TSH) in the sample.
Aufbereitung der Reagenzien
  • Bring all kit components and samples to room temperature (18-25°C) before use.
  • Standard - Reconstitute the Standard with 0.5mL 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 4,000pg/mL. Please prepare 5 tubes containing 0.6mL Standard Diluent and produce a triple dilution series. Mix each tube thoroughly before the next transfer. Set up 5 points of diluted standard such as 4,000pg/mL, 1,333.3pg/mL, 444.4pg/mL, 148.1pg/mL, 49.4pg/mL, and the last EP tubes with Standard Diluent is the blank as 0pg/mL.
  • Assay Diluent A and Assay Diluent B - Dilute 6mL of Assay Diluent A or B Concentrate(2×) with 6mL of deionized or distilled water to prepare 12 mL of Assay Diluent A or B. (In fact, more than 6mL Assay Diluent A and Assay Diluent B are contained in the bottles. Therefore, in every test, please precisely pipette required amount of Diluent and make double dilution in a new container. The prepared working dilution cannot be frozen.)
  • Detection Reagent A and Detection Reagent B - Briefly spin or centrifuge the stock Detection A and Detection B before use. Dilute to the working concentration with working Assay Diluent A or B, respectively (1:100).
  • Wash Solution - Dilute 20mL of Wash Solution concentrate (30×) with 580mL of deionized or distilled water to prepare 600 mL of Wash Solution (1×).
  • 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 standard within 15 minutes before assay. Please do not dissolve the reagents at 37°C directly.
  • Detection Reagent A and B are sticky solutions, therefore, slowly pipette them to reduce the volume errors.
  • 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 once 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 (30×), 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.
Probennahme Serum: Allow samples to clot for two hours at room temperature or overnight at 4°C before centrifugation for 20 minutes at approximately 1000 × g. Assay immediately or store samples in aliquot at -20°C or -80°C. Avoid repeated freeze/thaw cycles.

Plasma: Collect plasma using EDTA or heparin as an anticoagulant. Centrifuge samples for 15 minutes at 1000 × g within 30 minutes of collection. Remove plasma and assay immediately or store samples in aliquot at -20°C or -80°C. Avoid repeated freeze/thaw cycles.

Biological Fluids: Centrifuge samples for 20 minutes at 1000 × g. Remove particulates and assay immediately or store samples in aliquot at -20 °C or -80 °C for later use. Avoid repeated freeze/thaw cycles.
Aufbereitung der Proben
  • We are only responsible for the kit itself, but not for the samples consumed during the assay. The user should calculate the possible amount of the samples used in the whole test. Please reserve sufficient samples in advance.
  • Please predict the concentration before assaying. If values for these are not within the range of the standard curve, users must determine the optimal sample dilutions for their particular experiments. Sample should be diluted by 0.01mol/L PBS(PH=7.0-7.2).
  • If the samples are not indicated in the manual, a preliminary experiment to determine the validity of the kit is necessary.
  • Tissue or cell extraction samples prepared by chemical lysis buffer may cause unexpected ELISA results due to the impacts from certain chemicals.
  • Due to the possibility of mismatching between antigen from other origin and antibody used in our kits (e.g.antibody targets conformational epitope rather than linear epitope), some native or recombinant proteins from other manufacturers may not be recognized by our products.
  • Influenced by the factors including cell viability, cell number or sampling time, samples from cell culture supernatant may not be detected by the kit.
  • Fresh samples without long time storage is recommended for the test. Otherwise, protein degradation and denaturalization may occur in those samples and finally lead to wrong results.
Testdurchführung
  1. Prepare all reagents, samples and standards,
  2. Add 50μL standard or sample to each well.
    And then add 50μL prepared Detection Reagent A immediately.
    Shake and mix. Incubate 1 hour at 37 °C,
  3. Aspirate and wash 3 times,
  4. Add 100μL prepared Detection Reagent B. Incubate 30 minutes at 37 °C,
  5. Aspirate and wash 5 times,
  6. Add 90μL Substrate Solution. Incubate 10-20 minutes at 37 °C,
  7. Add 50μL Stop Solution. Read at 450 nm immediately.
Ergebnisberechnung

This assay employs the competitive inhibition enzyme immunoassay technique, so there is an inverse correlation between TSH concentration in the sample and the assay signal intensity. Average the duplicate readings for each standard, control, and samples. Create a standard curve on log-log or semi-log graph paper, with the log of TSH concentration on the y-axis and absorbance on the x-axis. Draw the best fit straight line through the standard points and it can be determined by regression analysis. Using some plot software, for instance, curve expert 1.30, is also recommended. If samples have been diluted, the concentration read from the standard curve must be multiplied by the dilution factor.
In order to make the calculation easier, we plot the O.D. value of the standard (X-axis) against the log of concentration of the standard (Y-axis), although concentration is the independent variable and O.D. value is the dependent variable. The O.D. values of the standard curve may vary according to the conditions of assay performance (e.g. operator, pipetting technique, washing technique or temperature effects). Typical standard curve below is provided for reference only.

Testpräzision

Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Thyroid Stimulating Hormone (TSH) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Thyroid Stimulating Hormone (TSH) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
Intra-Assay: CV<10%
Inter-Assay: CV<12%

Beschränkungen Nur für Forschungszwecke einsetzbar
Vorsichtsmaßnahmen The Stop Solution suggested for use with this kit is an acid solution. Wear eye, hand, face, and clothing protection when using this material.
Handhabung

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.

Lagerung 4 °C
Informationen zur Lagerung
  • 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.
Haltbarkeit 6 months
Bilder des Herstellers
ELISA image for Thyroid Stimulating Hormone (TSH) ELISA Kit (ABIN3159158) Thyroid Stimulating Hormone (TSH) ELISA Kit
Produkt verwendet in: Cao, Hua, Wang, Chen: "Exposure of pregnant mice to triclosan impairs placental development and nutrient transport." in: Scientific reports, Vol. 7, pp. 44803, 2017 (PubMed).

Le Stunff, Tilotta, Sadoine, Le Denmat, Briet, Motte, Clauser, Bougnères, Chaussain, Silve: "Knock-In of the Recurrent R368X Mutation of PRKAR1A that Represses cAMP-Dependent Protein Kinase A Activation: A Model of Type 1 Acrodysostosis." in: Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, Vol. 32, Issue 2, pp. 333-346, 2016 (PubMed).

Feng, Cao, Zhao, Wang, Hua, Chen, Chen: "Exposure of Pregnant Mice to Perfluorobutanesulfonate Causes Hypothyroxinemia and Developmental Abnormalities in Female Offspring." in: Toxicological sciences : an official journal of the Society of Toxicology, Vol. 155, Issue 2, pp. 409-419, 2016 (PubMed).

OHara, Curley, Tedim Ferreira, Cruickshanks, Milne, Smith: "Pituitary androgen receptor signalling regulates prolactin but not gonadotrophins in the male mouse." in: PLoS ONE, Vol. 10, Issue 3, pp. e0121657, 2015 (PubMed).

Zhang, Song, Feng, Zhou, Lu, Gao, Yu, Jiang, Zhao: "Thyroid-stimulating hormone decreases HMG-CoA reductase phosphorylation via AMP-activated protein kinase in the liver." in: Journal of lipid research, Vol. 56, Issue 5, pp. 963-71, 2015 (PubMed).

Abdulrahman, Boon, Sips, Guigas, Rensen, Smit, Hovens: "Impact of Metformin and compound C on NIS expression and iodine uptake in vitro and in vivo: a role for CRE in AMPK modulation of thyroid function." in: Thyroid : official journal of the American Thyroid Association, Vol. 24, Issue 1, pp. 78-87, 2014 (PubMed).

Sterle, Valli, Cayrol, Paulazo, Martinel Lamas, Diaz Flaqué, Klecha, Colombo, Medina, Cremaschi, Barreiro Arcos: "Thyroid status modulates T lymphoma growth via cell cycle regulatory proteins and angiogenesis." in: The Journal of endocrinology, Vol. 222, Issue 2, pp. 243-55, 2014 (PubMed).

Sauer, Brigida, Carriglio, Hernandez, Scaramuzza, Clavenna, Sanvito, Poliani, Gagliani, Carlucci, Tabucchi, Roncarolo, Traggiai, Villa, Aiuti: "Alterations in the adenosine metabolism and CD39/CD73 adenosinergic machinery cause loss of Treg cell function and autoimmunity in ADA-deficient SCID." in: Blood, Vol. 119, Issue 6, pp. 1428-39, 2012 (PubMed).

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