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Orient New Life Medical Co.,Ltd.

  • China,Ningbo ,Zhejiang
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China TriiodothyronineT3 Elisa Kit Test Goat - Anti - Mouse Antibody Coated Microtiter
China TriiodothyronineT3 Elisa Kit Test Goat - Anti - Mouse Antibody Coated Microtiter

  1. China TriiodothyronineT3 Elisa Kit Test Goat - Anti - Mouse Antibody Coated Microtiter

TriiodothyronineT3 Elisa Kit Test Goat - Anti - Mouse Antibody Coated Microtiter

  1. MOQ: 10 kit
  2. Price:
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Payment Terms T/T, Western Union
Supply Ability 100000kit/month
Delivery Time 20-35days
Packaging Details 96T/kit
Method Elisa kit
Format 96T/KIT
Valid 24 month
Accuracy 99.92%
Sensitivity 99.91%
Application T3
Brand Name New Life
Model Number 96 wells
Certification ISO, CE
Place of Origin China

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  1. Product Details
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Product Specification

Payment Terms T/T, Western Union Supply Ability 100000kit/month
Delivery Time 20-35days Packaging Details 96T/kit
Method Elisa kit Format 96T/KIT
Valid 24 month Accuracy 99.92%
Sensitivity 99.91% Application T3
Brand Name New Life Model Number 96 wells
Certification ISO, CE Place of Origin China
High Light rapid elisa testelisa assay kit

TriiodothyronineT3 ELISA test , high accuracy, Elisa Sandwich method, for quantitative measurement

 

Product Name: TriiodothyronineT3 ELISA test

 

 

Intended Use:

 

This Total T3 EIA is intended for the quantitative determination of triiodothyronine (T3) concentration in human serum. This test is useful in the diagnosis and treatment of thyroid diseases such as hyperthyroidism.

 

Summary:

 

Measurement of serum triiodthyronine concentration is generally regarded as a valuable tool in the diagnosis of thyroid dysfunction. This importance has provided the impetus for the significant improvement in assay methodology that has occurred in the last two decades. The advent of monospecific antiserum and the discovery of blocking agents to the T3 binding serum proteins has enabled the development of procedurally simple radioimmunoassays

 

Principle of Test:

 

The Total Triiodthyronine (T3) ELISA Kit is a solid phase enzyme-linked immunosorbent assay (ELISA) based on the principle of competitive binding. The microtiter wells are coated with a polyclonal goat-anti-mouse antibody. Standards, controls and patient serum incubate together with Assay Reagent containing monoclonal anti-T3 antibodies. In the following incubation with Conjugate the endogenous T3 of a patient sample competes with the T3-horseradish peroxidase conjugate for a limited number of insolubilized binding sites. After incubation the unbound conjugate is washed off. The amount of bound peroxidase conjugate is inversely proportional to the concentration of T3 in the sample. After addition of the substrate solution, the intensity of colour developed is inversely proportional to the concentration of T3 in the patient sample.

 

Kit Components

 

  1. Microtiterwells, 12 x 8 (break apart) strips, 96 wells; Wells coated with Treponema pallidum antigen. (incl. 1 strip holder and 1 cover foil)
  2. Pos. Control ***, 1 vial, 1.0 mL, ready to use; colored yellow, red cap.
  3. Neg. Control ***, 1 vial, 2.0 mL, ready to use; colored yellow, yellow cap.
  4. Cut-off Control ***, 1 vial, 1.0 mL, ready to use; colored yellow, black cap.
  5. Enzyme Conjugate **, 1 vial, 13 mL, ready to use,
  6. Substrate Solution, 1 vial, 14 mL, ready to use, Tetramethylbenzidine (TMB).
  7. Stop Solution, 1 vial, 14 mL, ready to use, contains 0.2 mol/l H2SO4, Avoid contact with the stop solution. It may cause skin irritations and burns.
  8. Wash Solution *, 1 vial, 30 mL (20X concentrated for 600 mL), pH 7.2 ± 0.2 see „Preparation of Reagents“.

* contains 0.03 % ProClin 300

** contains 0.03 % ProClin 300 + 0.01 % Gentamicin sulphate

*** contains 0.03 % ProClin 300 + 0.015 % 5-bromo-5-nitro-1,3-dioxane (BND) + 0.010 % 2-methyl-2H-isothiazol-3-one (MIT)

 

 

ASSAY PROCEDURE

 

1. Secure the desired number of Microtiter wells in the frame holder.

 

2. Dispense 10 µL of each Standard, Control and samples with new disposable tips into appropriate wells.

 

3. Incubate for 5 minutes at room temperature (18 °C – 25 °C).

 

4. Dispense 100 µL Enzyme Conjugate into each well.

Thoroughly mix for 10 seconds. It is important to have a complete mixing in this step.

 

5. Incubate for 80 minutes at room temperature (18 °C – 25 °C).

 

6. Briskly shake out the contents of the wells.

 

Rinse the wells 5 times with diluted Wash Solution (400 µL per well). Strike the wells sharply on absorbent paper to remove residual droplets.

 

 

 

 

 

 

 

 

 

PERFORMANCE CHARACTERISTICS

 

 

1. Sensitivity

 

The sensitivity of this Total T3 EIA test is defined as the lowest concentration of T3 that can be distinguished from 0 ng/mL as calculated from the 95% confidence limits of the 0 ng/mL standard absorbance. This method will reliably detect T3 concentrations as low as 0.2 ng/ml.

 

2. Precision

 

a. Intra-Assay Precision

 

Within-run precision was determined by replicate determinations of three different control sera in 1 assay.

 

Serum Sample 1 2 3
Number of Replicates 20 20 20
Mean T3 (ng/mL) 0.85 2.48 4.41
Standard Deviation 0.08 0.10 0.14
Coefficient of Variation (%) 9.6% 4.1% 3.2%

 

b. Inter-Assay Precision

 

Between-run precision was determined by replicate measurements of three different serum samples over a series of individually calibrated assays.

 

Serum Sample 1 2 3
Number of Replicates 20 20 20
Mean T3 (ng/mL) 0.79 2.53 4.10
Standard Deviation 0.08 0.08 0.06
Coefficient of Variation (%) 10.3% 3.2% 1.4%

 

3. Recovery and Linearity Studies

 

a. Recovery

Various patient serum samples of known T3 levels were combined and assayed in duplicate. The mean recovery was 106%.

 

Expected Conc. (ng/mL) Observed Conc. (ng/mL) % Recovery
5.05 4.1 99%
2.71 2.73 101%
1.46 1.52 104%
0.68 0.65 96%
  Mean Recovery #1 = 100 %
5.81 6.16 106%
3.02 3.17 105%
1.54 1.75 114%
0.71 0.84 119%

Mean Recovery #2 = 111 %

 

  1. Linearity

Two samples were serially diluted with zero T3 standard to determine linearity. The mean recovery was 99%.

 

  # Dilution Expected Conc. (ng/mL) Observed Conc. (ng/mL)   % Expected
  1. Undiluted ---- 6.06   ----
    1:2 3.03 3.05   101%
    1:4 1.51 1.46   97%
    1:8 0.75 0.68   91%
          Average = 96%
  2. Undiluted ---- 5.66   ----
    1:2 2.83 2.86   101%
    1:4 1.42 1.55   109%
    1:8 0.71 0.67   94%

Average = 101%

 

 
 
ORIENT NEW LIFE MEDICAL CO., LTD.
Contact: Jerry Meng
Email: Jerry @ newlifebiotest .com
Tel. +86 18657312116
SKYPE enetjerry
 

Company Details

Bronze Gleitlager

,

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 and 

Graphite Plugged Bushings

 from Quality China Factory
  • Business Type:

    Manufacturer,Exporter

  • Year Established:

    2009

  • Total Annual:

    10,000,000-15,000,000

  • Employee Number:

    200~300

  • Ecer Certification:

    Active Member

Established in 2009, Orient New Life Medical Co., Ltd., is specialized in high-tech biological diagnostic test development, research and production, as well as high-tech medical device development, research and production. New Life has built up two production base, which produce biological diagnosti... Established in 2009, Orient New Life Medical Co., Ltd., is specialized in high-tech biological diagnostic test development, research and production, as well as high-tech medical device development, research and production. New Life has built up two production base, which produce biological diagnosti...

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  • Orient New Life Medical Co.,Ltd.
  • 12F,Guting Building,Hefeng Creative Square,No.495 Jiangdong North Road,Ningbo,Zhejiang, China
  • https://www.medicaldiagnostictestkits.com/

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