CLIA Kit for Major Basic Protein (MBP)
PRG2; BMPG; Proteoglycan 2; Bone Marrow,Natural Killer Cell Activator; Eosinophil Granule Major Basic Protein; Proteoglycan 2,Bone Marrow; Pregnancy-associated major basic
- Product No.SCB650Mu
- Organism SpeciesMus musculus (Mouse) Same name, Different species.
- Sample TypeSerum, plasma, tissue homogenates, cell lysates and other biological fluids
- Test MethodDouble-antibody Sandwich
- Assay Length2h, 40min
- Detection Range54.9-40,000pg/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 18.8pg/mL.
- DownloadInstruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
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This assay has high sensitivity and excellent specificity for detection of Major Basic Protein (MBP).
No significant cross-reactivity or interference between Major Basic Protein (MBP) and analogues was observed.
Matrices listed below were spiked with certain level of recombinant Major Basic Protein (MBP) and the recovery rates were calculated by comparing the measured value to the expected amount of Major Basic Protein (MBP) in samples.
|Matrix||Recovery range (%)||Average(%)|
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Major Basic Protein (MBP) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Major Basic Protein (MBP) were tested on 3 different plates, 8 replicates in each plate.
CV(%) = SD/meanX100
The linearity of the kit was assayed by testing samples spiked with appropriate concentration of Major Basic Protein (MBP) and their serial dilutions. The results were demonstrated by the percentage of calculated concentration to the expected.
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
|Pre-coated, ready to use 96-well strip plate||1||Plate sealer for 96 wells||4|
|Detection Reagent A||1×120µL||Assay Diluent A||1×12mL|
|Detection Reagent B||1×120µL||Assay Diluent B||1×12mL|
|Substrate A||1×10mL||Substrate B||1×2mL|
|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 100µL Substrate Solution. Incubate 10 minutes at 37°C;
8. Read RLU value immediately.
|Evid Based Complement Alternat Med||Inhibitory Action of Quercetin on Eosinophil Activation In Vitro PubMed: PMC3690238|
|Catalog No.||Related products for research use of Mus musculus (Mouse) Organism species||Applications (RESEARCH USE ONLY!)|
|RPB650Mu01||Recombinant Major Basic Protein (MBP)||Positive Control; Immunogen; SDS-PAGE; WB.|
|RPB650Mu02||Recombinant Major Basic Protein (MBP)||Positive Control; Immunogen; SDS-PAGE; WB.|
|PAB650Mu02||Polyclonal Antibody to Major Basic Protein (MBP)||WB; IHC; ICC; IP.|
|PAB650Mu01||Polyclonal Antibody to Major Basic Protein (MBP)||WB; IHC; ICC; IP.|
|LAB650Mu71||Biotin-Linked Polyclonal Antibody to Major Basic Protein (MBP)||WB; IHC; ICC.|
|SEB650Mu||ELISA Kit for Major Basic Protein (MBP)||Enzyme-linked immunosorbent assay for Antigen Detection.|
|SCB650Mu||CLIA Kit for Major Basic Protein (MBP)||Chemiluminescent immunoassay for Antigen Detection.|