ArtNr |
SCB560Mu-10x96T |
Hersteller |
Cloud-Clone
|
Menge |
10x96T |
Kategorie |
|
Typ |
Elisa-Kit |
Specific against |
Mouse |
ECLASS 10.1 |
32160605 |
ECLASS 11.0 |
32160605 |
UNSPSC |
41116126 |
Alias |
LT-B, p33, TNFC, TNF-C, TNFSF3, Tumor necrosis factor ligand superfamily member 3, Tumor Necrosis Factor C |
Lieferbar |
|
Quantity options |
|
Detection range |
1.37-1, 000pg/mL |
Organism species |
Mus musculus (Mouse) |
Sensitivity |
The minimum detectable dose of this kit is typically less than 0.59pg/mL |
Sample type |
Serum, plasma, tissue homogenates, cell lysates and other biological fluids |
Assay length |
2h, 40min |
Method |
Double-antibody Sandwich |
Specificity |
This assay has high sensitivity and excellent specificity for detection of Lymphotoxin Beta (LTb). No significant cross-reactivity or interference between Lymphotoxin Beta (LTb) and analogues was observed. |
Precision |
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Lymphotoxin Beta (LTb) were tested 20 times on one plate, respectively. Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Lymphotoxin Beta (LTb) 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 37° C; 3. Aspirate and add 100µ L prepared Detection Reagent A. Incubate 1 hour at 37° C; 4. Aspirate and wash 3 times; 5. Add 100µ L prepared Detection Reagent B. Incubate 30 minutes at 37° C; 6. Aspirate and wash 5 times; 7. Add 100µ L Substrate Solution. Incubate 10 minutes at 37° C; 8. Read RLU value immediately. |
Test principle |
The microplate provided in this kit has been pre-coated with an antibody specific to Lymphotoxin Beta (LTb). Standards or samples are then added to the appropriate microplate wells with a biotin-conjugated antibody specific to Lymphotoxin Beta (LTb). 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 Lymphotoxin Beta (LTb) level in the sample or standard.; |
Research Area |
Cytokine; Tumor immunity; Infection immunity; |
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