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ELK Biotechnology
SKU:ELK4710
Human y+LAT1(L-Type Amino Acid Transporter 1) ELISA Kit
Human y+LAT1(L-Type Amino Acid Transporter 1) ELISA Kit
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Human y+LAT1(L-Type Amino Acid Transporter 1) ELISA Kit
Overview
| Product name: | Human y+LAT1(L-Type Amino Acid Transporter 1) ELISA Kit |
| Reactivity: | Human |
| Alternative Names: | SLC7A7; LPI; Y+LAT1; MOP-2; Monocyte amino acid permease 2; Y+L Amino Acid Transporter 1; Solute Carrier Family 7 Member 7,Cationic Amino Acid Transporter,y+ System |
| Assay Type: | Sandwich |
| Sensitivity: | 0.114 ng/mL |
| Standard: | 20 ng/mL |
| Range: | 0.32-20 ng/mL |
| Sample Type: | Tissue homogenates, cell lysates and other biological fluids. |
| Assay Length: | 3.5h |
| Research Area: | Signal transduction; |
| 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 Human y+LAT1. Standards or samples are added to the appropriate microtiter plate wells then with a biotin-conjugated antibody specific to Human y+LAT1. 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 Human y+LAT1, 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 Human y+LAT1 in the samples is then determined by comparing the OD of the samples to the standard curve. |
Standard curve
| Concentration (ng/mL) | OD | Corrected OD |
|---|---|---|
| 20.00 | 2.153 | 2.049 |
| 10.00 | 1.562 | 1.458 |
| 5.00 | 1.144 | 1.040 |
| 2.50 | 0.877 | 0.773 |
| 1.25 | 0.593 | 0.489 |
| 0.63 | 0.239 | 0.135 |
| 0.32 | 0.187 | 0.083 |
| 0.00 | 0.104 | 0.000 |

Precision
Intra-assay Precision (Precision within an assay):CV%<8%
Three samples of known concentration were tested twenty times on one plate to assess intra-assay precision.
Inter-assay Precision (Precision between assays):CV%<10%
Three samples of known concentration were tested in forty separate assays to assess inter-assay precision.
Recovery
Matrices listed below were spiked with certain level of recombinant y+LAT1 and the recovery rates were calculated by comparing the measured value to the expected amount of y+LAT1 in samples.
| Matrix | Recovery range | Average |
|---|---|---|
| serum(n=5) | 89-103% | 96% |
| EDTA plasma(n=5) | 86-99% | 92% |
| Heparin plasma(n=5) | 83-97% | 90% |
Linearity
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of y+LAT1 and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
| Matrix | 1:2 | 1:4 | 1:8 | 1:16 |
|---|---|---|---|---|
| serum(n=5) | 88-99% | 81-93% | 89-97% | 85-94% |
| EDTA plasma(n=5) | 87-96% | 82-95% | 93-102% | 87-96% |
| Heparin plasma(n=5) | 93-106% | 87-99% | 85-93% | 79-96% |
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