Comparison

Mouse Anti-Thyroglobulin Antibody (Anti-TG) ELISA Kit

Manufacturer Biomatik
Category
Type ELISA Kits
Specific against Mouse
Amount 96T
Item no. BM-EKU12127
eClass 6.1 32160605
eClass 9.0 32160605
Available
Format
96-Well Plate
Target Name
Anti-TG / Anti-Thyroglobulin Antibody
Target Synonyms
AITD3; TGN
Sample Type
serum, plasma and other biological fluids
Detection Range
3.12-200ng/mL
Sensitivity
1.21ng/mL
Precision
Intra-Assay: CV<10%, Inter-Assay: CV<12%
Detection Method
Competitive Inhibition
Assay Time
2.5 hours
Application
ELISA
Assay Type
Competitive Inhibition
Shipping Condition
Ice packs
Storage
Short term: 4°C; Long term: see manual.
Precaution of Use
The Stop Solution is acidic. Do not allow to contact skin or eyes.
Expiry Date
8 months
UniProt ID
O08710
Specificity
This assay has high sensitivity and excellent specificity for detection of Anti-Thyroglobulin Antibody (Anti-TG). No significant cross-reactivity or interference between Anti-Thyroglobulin Antibody (Anti-TG) and analogues was observed.
Test Principle
The test principle applied in this kit is Sandwich enzyme immunoassay. The microtiter plate provided in this kit has been pre-coated with an antibody specific to Paraoxonase 1 (PON1). Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody specific to Paraoxonase 1 (PON1). Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. After TMB substrate solution is added, only those wells that contain Paraoxonase 1 (PON1), biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450nm ± 10nm. The concentration of Paraoxonase 1 (PON1) in the samples is then determined by comparing the O.D. of the samples to the standard curve.
Assay Procedure Summary
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 5 times; 5. Add 90µl Substrate Solution. Incubate 10-20 minutes at 37°C ; 6. Add 50µl Stop Solution. Read at 450nm immediately.
Stability
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.
Restriction
For Research Use Only. Not for use in diagnostic procedures. Not for human or animal drug or food use.
Quality Systems
The kit is manufactured at ISO 9001 and ISO 13485 certified facilities.
Quality Assurance
Biomatik ELISA Kits are not typically pre-assembled as finished products due to limited shelf life. Before shipping, each kit is assembled and tested to ensure that it meets specifications before shipping. Minor changes may occur to the Detection Range, Sensitivity, and Precision. All kits are tested to confirm that they fall within their defined Inter- and Intra- assay coefficient of variation. Please always refer to the hard copy manual included in the kit before experiment.
Research Area
Metabolic pathway; Endocrinology;

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 96T
Available: In stock
available

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