Item no. |
SCA190Hu-5x96T |
Manufacturer |
Cloud-Clone
|
Amount |
5x96T |
Category |
|
Type |
Clia |
Applications |
CLIA |
Specific against |
Human |
ECLASS 10.1 |
32161000 |
ECLASS 11.0 |
32161000 |
UNSPSC |
41116126 |
Alias |
Glycosylated Hemoglobin, Hemoglobin A1c, Hb1c, HbAIc, HbAIc |
Available |
|
Quantity options |
|
Quantity options |
|
Alternative Names |
Glycosylated Hemoglobin, Hemoglobin A1c, Hb1c, HbAIc, HbAIc |
Detection range |
0.82-600ng/mL The standard curve concentrations used for the CLIA’s were 600ng/mL, 200ng/mL, 66.67ng/mL, 22.22ng/mL, 7.41ng/mL, 2.47ng/mL, 0.82ng/mL |
Sensitivity |
The minimum detectable dose of this kit is typically less than 035ng/mL |
Sample type |
Plasma |
Assay length |
4.5 hours |
Method |
Sandwich |
Specificity |
This assay has high sensitivity and excellent specificity for detection of Glycated Hemoglobin A1c (HbA1c). No significant cross-reactivity or interference between Glycated Hemoglobin A1c (HbA1c) and analogues was observed. |
Precision |
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Glycated Hemoglobin A1c (HbA1c) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Glycated Hemoglobin A1c (HbA1c) were tested on 3 different plates, 8 replicates in each plate. CV(%) = SD/meanX100 Intra-Assay: CV<10% Inter-Assay: CV<12% |
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. |
Assay procedure summary |
1. Prepare all reagents, samples and standards; 2. Add 100µ L standard or sample to each well. Incubate 2 hours at 37oC; 3. Aspirate and add 100µ L prepared Detection Reagent A. Incubate 1 hour at 37oC; 4. Aspirate and wash 3 times; 5. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37oC; 6. Aspirate and wash 5 times; 7. Add 100µ L Substrate Solution. Incubate 10 minutes at 37oC; 8. Read RLU value immediately. |
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 biotin-conjugated secondary antibody. Next, Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then the mixture of substrate A and B is added to generate glow light emission kinetics. Upon plate development, the intensity of the emitted light is proportional to the Fibrinogen (FG) level in the sample or standard. |
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.