SKU(재고 관리 코드):SEA217Ra
ELISA Kit for Alpha-1-Microglobulin (a1M)
ELISA Kit for Alpha-1-Microglobulin (a1M)
Enzyme-linked immunosorbent assay for Antigen Detection.
Product No.
SEA217Ra
Organism Species
Rattus norvegicus (Rat).
Sample Type
serum, plasma, urine and other biological fluids
Test Method
Double-antibody Sandwich
Assay Length
3h
Detection Range
1.56-100ng/mL
Sensitivity
The minimum detectable dose of this kit is typically less than 0.73ng/mL.
UOM
48T 96T 96T*5 96T*10 96T*100
Specificity
This assay has high sensitivity and excellent specificity for detection of Alpha-1-Microglobulin (a1M).
No significant cross-reactivity or interference between Alpha-1-Microglobulin (a1M) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant Alpha-1-Microglobulin (a1M) and the recovery rates were calculated by comparing the measured value to the expected amount of Alpha-1-Microglobulin (a1M) in samples.
Matrix | Recovery range (%) | Average(%) |
serum(n=5) | 84-98 | 92 |
EDTA plasma(n=5) | 84-101 | 93 |
heparin plasma(n=5) | 91-101 | 96 |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Alpha-1-Microglobulin (a1M) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Alpha-1-Microglobulin (a1M) 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 Alpha-1-Microglobulin (a1M) 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) | 82-98% | 84-103% | 98-105% | 84-101% |
EDTA plasma(n=5) | 97-105% | 85-99% | 91-103% | 87-95% |
heparin plasma(n=5) | 81-99% | 95-104% | 97-105% | 93-101% |
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 |
Detection Reagent B | 1×120µL | Assay Diluent B | 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 3 times;
5. Add 100µL prepared Detection Reagent B. Incubate 30 minutes at 37°C;
6. Aspirate and wash 5 times;
7. Add 90µL Substrate Solution. Incubate 10-20 minutes at 37°C;
8. Add 50µL Stop Solution. Read at 450nm immediately.
Magazine | Citations |
Diabetes Technology & Therapeutics | Proteomic Identification of Human Urinary Biomarkers in Diabetes Mellitus Type 2 Liebert: 20100078 |
Journal of Pharmaceutical and Biomedical Analysis | Effect of high dose thiamine on the levels of urinary protein biomarkers in diabetes mellitus type 2 PubMed: 21130593 |
BioMed Research International | Proteomic Profiling for Peritoneal Dialysate: Differential Protein Expression in Diabetes Mellitus PubMed: PMC3679811 |
Mainz | Identifizierung neuer potentieller Biomarker für das Kolonkarzinom sowie dessen Vorstufen Info:Source |
Cellular Physiology and Biochemistry | Activated Α7nachr Improves Postoperative Cognitive Dysfunction and Intestinal Injury Induced by Cardiopulmonary Bypass in Rats: Inhibition of the Proinflammatory … Pubmed:29672286 |
Journal of Clinical Medicine | Urinary Proteomics for the Early Diagnosis of Diabetic Nephropathy in Taiwanese Patients Pubmed: 30486327 |
Catalog No. | Related products for research use of Rattus norvegicus (Rat) Organism species | Applications (RESEARCH USE ONLY!) |
RPA217Ra01 | Recombinant Alpha-1-Microglobulin (a1M) | Positive Control; Immunogen; SDS-PAGE; WB. |
RPA217Ra02 | Recombinant Alpha-1-Microglobulin (a1M) | Positive Control; Immunogen; SDS-PAGE; WB. |
PAA217Ra01 | Polyclonal Antibody to Alpha-1-Microglobulin (a1M) | WB; IHC; ICC; IP. |
PAA217Ra02 | Polyclonal Antibody to Alpha-1-Microglobulin (a1M) | WB; IHC; ICC; IP. |
LAA217Ra81 | FITC-Linked Polyclonal Antibody to Alpha-1-Microglobulin (a1M) | WB; IHC; ICC; IF. |
LAA217Ra71 | Biotin-Linked Polyclonal Antibody to Alpha-1-Microglobulin (a1M) | WB; IHC; ICC. |
SEA217Ra | ELISA Kit for Alpha-1-Microglobulin (a1M) | Enzyme-linked immunosorbent assay for Antigen Detection. |
LMA217Ra | Magnetic Luminex Assay Kit for Alpha-1-Microglobulin (a1M) ,etc. | Magnetic Luminex Assay for Antigen Detection. |