Total T3 (Triiodothyronine) MICRO-ELISA Test Kit

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Product No.T181
Protein
Triiodothyronine
Formats AvailableView All
Product Type
ELISA Kit
Applications
ELISA
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T181-96 tests
96 tests
$220.00
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Step: 1

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Product Details

Description

The MICRO EIA TRIIODOTHYRONINE (T3) test is a solid phase
competitive enzyme immunoassay (EIA) Kit for the In vitro quantitative
determination of triiodothyronine (T3) concentration in human serum.

Materials Provided
Components in Each 96-Test MICRO EIA T3 Diagnostic Kit

1.) 96 wells ANTIBODY COATED WELLS Coated with anti mouse (goat
polyclonal); contained in a pack with silica gel desiccant.
2.) 1 bottle 7.0 mL T3-ANTIBODY (mouse monoclonal) in a buffered protein
solution; contains a preservative.
3.) 1 bottle 1.3 mL T3-ENZYME CONJUGATE CONCENTRATE T3-labeled
horseradish peroxidase in a buffered protein solution; contains a
preservative.
4.) 1 bottle 13.0 mL ASSAY BUFFER Buffered protein solution with ANS and
sodium salicylate; contains a preservative.
5.) 1 vial 0.75 mL T3 SERUM STANDARD, 0 ng/dl. Human serum; contains
a preservative.
6.) 5 vials 0.75 mL T3 SERUM STANDARDS, 75, 150, 300, 600, AND 1000
ng/dl. Human serum with added T3; contains a preservative.
7.) 1 bottle 50.0 mL WASH BUFFER CONCENTRATE (20X) Buffered
detergent solution; contains a preservative. Dilute bottle to 1000 mL with
deionized water.
8.) 1 bottle 11.0 mL SUBSTRATE CHROMOGEN Buffered hydrogen peroxide
and 3,3',5,5' tetramethylbenzidine (TMB) solution.
9.) 1 bottle 11.0 mL STOP SOLUTION 1 N HCl.
Other Materials and Solutions Required
Additional Required Materials

Disposable tip precision pipet 0.025, 0.1, 0.2, and 1.0 mL
microtiter plate reader
Absorbent paper
Distilled or deionized water

Precautions

Patient sample may contain pathogens: treat all samples as potentially
infectious.


CAUTION: Source material used to prepare Standards was derived from
human material. The material was tested using FDA-approved methods
and found non-reactive for Hepatitis B Surface Antigen (HBsAg) by ELISA
and non-reactive for HIV by ELISA. No known test method can offer total
assurance that infectious agents are absent.

HANDLE THESE REAGENTS AS IF THEY ARE POTENTIALLY INFECTIOUS.


Information on handling human serum is provided in the CDC/NIH manual
"Bio-safety in Microbiological and Biomedical Laboratories" (1984).

Quality Control

Good laboratory practice requires that quality control specimens be run with each patient sample run to check the assay performance. Three controls with normal, low and elevated values should be used. Pooled human serum or commercially available control sera are suitable. Any material used should be assayed repeatedly to establish mean values and acceptable ranges to assure proper performance.
Do not mix or interchange reagent lots with any other kit of different kit lots.
Do not use reagents beyond the expiration date printed on each vial or bottle.

Reagent Preparation

WORKING CONJUGATE: Dilute only enough conjugate for a single
assay run. Dilute the conjugate 1:11 with the assay buffer. Prepare 0.1
mL of working conjugate for each well. Label the bottle and store at 2°-
8°C. Expiration time is 24 hours. If the absorbance of the 0 ng/mL
calibrator is higher than the absorbance that can be read on the
spectrophotometer; make a 1:15 dilution of the stock conjugate (instead of
the 1:11 dilution) by using 7 µL conjugate for each 0.1 mL of diluent.
Dilute the entire contents of the WASH BUFFER to 1,000 mL with
deionized water. Expiration date is the same as the concentrate. Store at
2°-8°C.

Assay Procedure

PREPARE WORKING CONJUGATE: TO AN ALIQUOT OF ASSAY BUFFER (0.1 mL for each

WELL) ADD THE REQUIRED VOLUME OF STOCK CONJUGATE (10 µL for each well). MIX GENTLY.

  1. Pipet 50 µL of T3 standards into the appropriate well. Pipet 50 µL of each control and patient serum into the appropriate well.
  2. Pipet 50 µL of T3 ANTIBODY REAGENT into all wells and mix gently for 30 seconds.
  3. Pipet 100 µL (0.1 mL) of freshworking T3-enzyme conjugate into all wells and mix gently for 30 seconds. It is important to have complete mixing in steps 2 and 3.
  4. Incubate at room temperature (18° 30°C) for 60 minutes ± 5 minutes.
  5. Decant or aspirate and discard liquid contents of all wells.
  6. Fill each well with diluted WASH BUFFER. Decant or aspirate liquid contents of all wells. Do not use tap water.

WARNING: WASHING THE WELLS IS OF CRITICAL IMPORTANCE. Fill the wells to overflowing, you CANNOT cause any carryover between wells. You CANNOT over wash the wells. Completely decant or aspirate all of the liquid out of the wells. SLAP the inverted wells on a FRESH clean piece of absorbent paper AFTER EACH WASH. YOU CANNOT SLAP TOO HARD, REMOVE ALL OF THE LIQUID FROM THE WELLS.

  1. Repeat step 6 twice more (for a total of 3 washes). Tap wells free of any liquid or aspirate thoroughly.
  2. Pipet or dispense 100 µL (0.1 mL) of SUBSTRATE / CHROMOGEN REAGENT into each well.
  3. Mix thoroughly and incubate 20 minutes at room temperature (18°-30°C).
  4. Pipet or dispense 100 µL of STOPPING REAGENT into each well and mix thoroughly.
  5. Read the absorbance of each well at 450 ± 10 nm against water within 15 minutes.
Calculation of Results

1. Calculate the %A/A0 value for each standard, control and sample.

    A    
%A/A0 =
× 100%
    A0    

A = the average absorbance value for the standard, controlsand patient samples.

A0 = the average absorbance value for the 0 µg/dl standard.


2. Construct a standard curve by plotting the %A/A0 value for the thyroxin
standards (vertical axis) versus the T4 standard concentration (horizontal
axis) on the logit-log graph paper supplied
3. Draw the best straight line through the points.
4. Interpolate the control and patient sample values from each %A/A0
value obtained.
5. Save the calibration curve for use in subsequent runs using only single
point calibration (0 µg/dl).
Optional calculation method for use with single point calibration and
stored standard calibration curve.

a. For single point calibration runs, calculate %A/A0 values for samples
and controls using the absorbance of the 0 µg/dl standard that was run
with them.
b. Using the original standard calibration curve, interpolate the control
and patient sample values from each %A/A0 value obtained in the run.
NOTE: For automated data reduction, use a log/logit date transformation
of A/A0 vs. T4 concentration.

 

EXAMPLE DATA

Specimen I.D

 

A450

%A/A0

Calculated Value

STANDARD 0 ng/dl

2.192

2.331

100%  
STANDARD 75 ng/dl

1.732

1.779

78%  
STANDARD 150 ng/dl

1.230

1.239

55%  
STANDARD 300 ng/dl

0.576

0.587

25%  
STANDARD 600 ng/dl

0.286

0.273

12%  
STANDARD 1000 ng/dl

0.176

0.171

8%  
PATIENT 1

1.157

1.192

52% 112 ng/dl
PATIENT 2

0.776

0.800

35% 188 ng/dl
PATIENT 3

0.294

0.281

13% 485 ng/dl

The range of this assay is 0 - 1000 ng/dl. For specimen with T3 concentrations beyond the standard curve (1000 ng/dl), repeat the test by diluting the
specimen with the 0 ng/dl Standard. To obtain the final concentration, multiply the concentration of the diluted sample by the dilution factor.

Background

The principal tests used in the laboratory evaluation of thyroid function are Total Thyroxin (T4), Total Triiodothyronine (T3), T-Uptake (T-Up), a calculated Free Thyroxin Index (FTI) and Thyroid Stimulating Hormone (TSH). The results of these tests are interrelated and help the clinician in making a diagnosis. Clinical hypothyroidism results from underproduction of thyroid hormones by the thyroid gland, consequently an abnormally low circulating T4 and T3 concentration in blood. Clinical hyperthyroidism results from excessive production of thyroid hormones and resulting elevation of T4 and T3 concentrations. The manifestations of thyroid dysfunction can result from disease of the thyroid gland (PRIMARY hyperthyroidism or hypothyroidism), disease of the pituitary gland (SECONDARY hyperthyroidism or hypothyroidism) or disease of the hypothalamus (TERTIARY hyperthyroidism or hypothyroidism). Thyroxin (3,5,3',5'-tetraiodo-l-thyronine, T4) and Triiodothyronine (3,5,3'- triiodo-l-thyronine, T3), are the hormones originating from the thyroid gland. T4 and T3 are responsible for regulating diverse biochemical processes throughout the body that are essential for protein synthesis, normal development, metabolic and neural activity. T4 is synthesized within the thyroid gland and secreted directly into the bloodstream. Approximately 30% of the circulating T4 is enzymatically deiodinated at the 5' position in the peripheral tissues to yield T3. The T4 likely serves as a "prohormone" for T3, which has a much greater metabolic activity. T4 and T3 are transported through the peripheral blood stream largely bound to serum proteins. The major transport protein is Thyroxin Binding Globulin (TBG) which normally accounts for 80% of the bound hormone. The other thyroid hormone binding proteins are Thyroxin Binding Prealbumin and Albumin. Only about 0.3% of the total serum T3 and only about 0.1% of the total serum T4 are unbound and free to diffuse into tissue to exert their biological effects. When the level of TBG increases, the level of total T4 will increase to maintain the same level of unbound or free T4 in the bloodstream of an euthyroid individual. Simply determining the total T4 concentration fails to take into account the variations in TBG levels that affect the unbound thyroxin (free T4) concentration. TBG levels can vary for reasons incidental to the patient's thyroid status such as the presence of certain drugs, steroid hormones, pregnancy, and various non-thyroidal diseases. The Thyroid Uptake (TUp) test is an indirect measurement of empty binding sites for T4 on the TBG molecule (unsaturated TBG) in the patient specimen. The number obtained from the multiplication of the Total T4 concentration by the Thyroid Uptake value is called a Free Thyroxin Index (FTI). The FTI correlates more closely with Free T4 (the metabolic active fraction) concentration than does the total T4 concentration alone. The FTI is therefore a better method of monitoring thyroid function and diagnosing thyroid illness than is a Total T4 determination alone. Diseases of the thyroid gland can result in clinical signs of thyroid dysfunction. Primary hypothyroidism results in underproduction of T4 by the thyroid gland and consequently an abnormally low circulating T4 concentration in the blood. Primary hyperthyroidism leads to excessive thyroid production of T4 and a resulting elevated T4 concentration. The determination of total serum T3 is used in the differential diagnosis of thyroid disease, particularly hyperthyroidism. In most hyperthyroid patients, both serum T3 and T4 are elevated. However, approximately 5- 10% of hyperthyroid patients have elevated T3 concentrations but normal serum T4, a condition known as T3-thyrotoxicosis. Such clinical conditions make it vital to establish that serum T3 is normal before excluding the diagnosis of hyperthyroidism. Serum T3 level is also an excellent indicator for the ability of the thyroid to respond to both stimulatory and suppressive tests. The thyroid gland function is regulated by the level of Thyroid Stimulating Hormone (TSH) which is produced and secreted by the pituitary gland. TSH is produced by the anterior lobe of the pituitary gland and acts on the thyroid gland to release thyroid hormones. The release of TSH from the pituitary is regulated by the hypothalamus when it secretes TRH (thyrotropin releasing hormone). In an euthyroid individual, the levels of thyroid hormones in the blood are inversely related to the levels of TSH and TRH. When the levels of thyroid hormones rise, the levels of TRH and TSH fall; and when the levels of thyroid hormones fall, the levels of TRH and TSH rise. In the event of failure of the thyroid gland, the levels of thyroid hormones fall and the negative feedback results in an elevated level of TSH in the blood. Elevated levels of TSH are thus useful in the diagnosis of primary hypothyroidism. Conversely, in the case of primary hyperthyroidism, the elevated levels of thyroid hormones will result in decreased levels of TSH. When there is a failure of the pituitary or the hypothalamus (secondary or tertiary hypothyroidism), the level of TSH is decreased in the presence of low levels of thyroid hormones. In secondary or tertiary hyperthyroidism, the level of TSH is increased in the presence of high levels of thyroid hormones.

References & Citations

1. Felig, P. et al. (1987) in Endocrinology and Metabolism (2nd ed.) McGraw-Hill Book Co., New York, NY p. 389
2. Sutherland, R. L. et al. (1975) J. Endocrinol. 65: 319
3. Ingbar, S. H. et al. (1960) Recent Progress in Hormone Research 16:353
4. Wilke, T. J. (1986) Clin. Chem. 32:585
5. Oppenheimer, J. H. (1968) N. Engl. J. Med. 278:1153
6. Sterling, K. et al. (1970) JAMA 213: 571
7. Witherspoon, L. R. et al. (1984) J. Clin. Immunoassay 7:192
8. Larsen, P. R. (1972) Metabolism 21: 1073
9. Ingbar, S. H. (1986) in Williams Textbook of Endocrinology Philadelphia, W. B. Saunders Co., p 682
Products are for research use only. Not for use in diagnostic or therapeutic procedures.
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