ELISA Kit for Anti-Insulin Receptor Antibody (Anti-INSR) Homo sapiens (Human) Antibody ELISA

CD220; ISR; HHF5; IR

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  • ELISA Kit for Anti-Insulin Receptor Antibody (Anti-INSR) Packages (Simulation)
  • ELISA Kit for Anti-Insulin Receptor Antibody (Anti-INSR) Packages (Simulation)
  • ELISA Kit for Anti-Insulin Receptor Antibody (Anti-INSR) Results demonstration
  • AEA895Hu.jpg Typical Standard Curve
  • Certificate ISO9001: 2008, ISO13485: 2003 Registered

Recovery

Matrices listed below were spiked with certain level of Anti-Insulin Receptor Antibody (Anti-INSR) and the recovery rates were calculated by comparing the measured value to the expected amount of Anti-Insulin Receptor Antibody (Anti-INSR) in samples.

Matrix Recovery range (%) Average(%)
serum(n=5) 91-105 99
EDTA plasma(n=5) 88-103 96
heparin plasma(n=5) 85-99 92

Precision

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

Linearity

The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Anti-Insulin Receptor Antibody (Anti-INSR) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.

Sample 1:2 1:4 1:8 1:16
serum(n=5) 79-101% 79-92% 79-104% 94-102%
EDTA plasma(n=5) 84-98% 99-105% 84-103% 95-104%
heparin plasma(n=5) 92-101% 95-105% 89-97% 94-102%

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.

Reagents and materials provided

Reagents Quantity Reagents Quantity
Pre-coated, ready to use 96-well strip plate 1 Plate sealer for 96 wells 4
Standard 2 Standard Diluent 1×20mL
Detection Reagent A 1×120µL Assay Diluent A 1×12mL
TMB Substrate 1×9mL Stop Solution 1×6mL
Wash Buffer (30 × concentrate) 1×20mL Instruction manual 1

Assay procedure summary

1. Prepare all reagents, samples and standards;
2. Add 100µL standard or sample to each well. Incubate 1 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.

ELISA Kit for Anti-Insulin Receptor Antibody (Anti-INSR)

Test principle

The microtiter plate provided in this kit has been pre-coated with an antigen. Standards or samples are then added to the appropriate microtiter plate wells with a Horseradish Peroxidase (HRP)-conjugated secondary antibody. After TMB substrate solution is added, those wells that contain Anti-Insulin Receptor Antibody (Anti-INSR) 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 Anti-Insulin Receptor Antibody (Anti-INSR) in the samples is then determined by comparing the O.D. of the samples to the standard curve.

Citations

  • Molecular and Biochemical Effect of Neem Extract On Experimental Diabetes Org:Source
  • Age-Dependent Onset of Insulin Resistance in Insulin-Resistant MicePubMed: 26632184
  • A newly developed silymarin nanoformulation as a potential antidiabetic agent in experimental diabetespubmed:27623396
  • Subcutaneous liraglutide ameliorates methylglyoxal-induced Alzheimer-like tau pathology and cognitive impairment by modulating tau hyperphosphorylation and glycogen synthase kinase-3β.pubmed:28337257
  • Vitamin D3 intake as regulator of insulin degrading enzyme and insulin receptor phosphorylationin diabetic rats.pubmed:27930980
  • Regulation of insulin receptor phosphorylation in the brains of prenatally stressed rats: New insight into the benefits of antidepressant drug treatment.pubmed:28063625
  • (台灣農業研究67 (4): 355-364) 香菇柄水萃物改善糖尿病降低阿茲海默氏症罹病風險初探
  • Mechanism underlying starvation-dependent modulation of olfactory behavior in Drosophila larvaPubmed: 32080342
  • Prenatal Stress Induced Spatial Memory Deficit in a Sex-Specific Manner in Mice: Possible Involvement of Hippocampal Insulin Resistance
  • Internal State Affects Local Neuron Function in an Early Sensory Processing Center to Shape Olfactory Behavior in Drosophila Larvae

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