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ELISA Kit for Mannose Binding Lectin (MBL)
MBL2; COLEC1; HSMBPC; MBP1; MBP; Collectin-1; Mannose-binding protein C; Mannan Binding Protein; Mannose-Binding Lectin(Protein C)2,Soluble(Opsonic Defect)
- Product No.SEB480Ra
- Organism SpeciesRattus norvegicus (Rat) Same name, Different species.
- Sample TypeSerum, plasma, tissue homogenates, cell lysates, cell culture supernates and other biological fluids.
- Test MethodDouble-antibody Sandwich
- Assay Length3h
- Detection Range0.312-20ng/mL
- SensitivityThe minimum detectable dose of this kit is typically less than 0.131ng/mL.
- DownloadInstruction Manual
- UOM 48T96T 96T*5 96T*10 96T*100
- FOB
US$ 505
For more details, please contact local distributors! US$ 722 US$ 3249 US$ 6137 US$ 50540
Specificity
This assay has high sensitivity and excellent specificity for detection of Mannose Binding Lectin (MBL).
No significant cross-reactivity or interference between Mannose Binding Lectin (MBL) and analogues was observed.
Recovery
Matrices listed below were spiked with certain level of recombinant Mannose Binding Lectin (MBL) and the recovery rates were calculated by comparing the measured value to the expected amount of Mannose Binding Lectin (MBL) in samples.
Matrix | Recovery range (%) | Average(%) |
serum(n=5) | 91-105 | 102 |
EDTA plasma(n=5) | 81-91 | 85 |
heparin plasma(n=5) | 97-105 | 101 |
Precision
Intra-assay Precision (Precision within an assay): 3 samples with low, middle and high level Mannose Binding Lectin (MBL) were tested 20 times on one plate, respectively.
Inter-assay Precision (Precision between assays): 3 samples with low, middle and high level Mannose Binding Lectin (MBL) 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 Mannose Binding Lectin (MBL) 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) | 95-103% | 93-101% | 78-101% | 86-97% |
EDTA plasma(n=5) | 79-91% | 82-96% | 81-90% | 94-101% |
heparin plasma(n=5) | 92-99% | 98-105% | 79-97% | 95-102% |
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.
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Magazine | Citations |
American Journal of Nephrology | Analysis of the Urine Proteome of Human Contrast-Induced Kidney Injury Using Two-Dimensional Fluorescence Differential Gel Electrophoresis/Matrix-Assisted Laser Desorption Time-of-Flight Mass Spectrometry/Liquid Chromatography Mass Spectrometry. Karger: 000255439 |
Current Eye Research | Serum Levels and H/L Gene Polymorphism of Mannose-Binding Lectin in Primary Open Angle Glaucoma Ingenta: art00007 |
Journal of Clinical Immunology | Complement activation contributes to the injury and outcome of kidney in human anti-glomerular basement membrane disease. PubMed: 22941511 |
Clinical and Experimental Immunology | Urinary mannose-binding lectin is a biomarker for predicting the progression of immunoglobulin (Ig)A nephropathy PubMed: PMC3406374 |
Clin J Am Soc Nephrol. | Alternative Complement Pathway Activation Products in Urine and Kidneys of Patients with ANCA-Associated GN Pubmed: 24115193 |
ACTA TROPICA | Novel findings on the role of ficolins and colectins in the innate response against Leishmania braziliensis Pubmed: 32827456 |
PLoS One | Complement activation profile of patients with primary focal segmental glomerulosclerosis Pubmed: 32569286 |
LIFE SCIENCES | The lectin pathway of complement and the initial recognition of Leishmania infantum promastigotes 34242658 |
Catalog No. | Related products for research use of Rattus norvegicus (Rat) Organism species | Applications (RESEARCH USE ONLY!) |
RPB480Ra02 | Recombinant Mannose Binding Lectin (MBL) | Positive Control; Immunogen; SDS-PAGE; WB. |
RPB480Ra01 | Recombinant Mannose Binding Lectin (MBL) | Positive Control; Immunogen; SDS-PAGE; WB. |
PAB480Ra02 | Polyclonal Antibody to Mannose Binding Lectin (MBL) | WB; IHC; ICC; IP. |
PAB480Ra01 | Polyclonal Antibody to Mannose Binding Lectin (MBL) | WB; IHC; ICC; IP. |
LAB480Ra71 | Biotin-Linked Polyclonal Antibody to Mannose Binding Lectin (MBL) | WB; IHC; ICC. |
SEB480Ra | ELISA Kit for Mannose Binding Lectin (MBL) | Enzyme-linked immunosorbent assay for Antigen Detection. |
LMB480Ra | Multiplex Assay Kit for Mannose Binding Lectin (MBL) ,etc. by FLIA (Flow Luminescence Immunoassay) | FLIA Kit for Antigen Detection. |
KSB480Ra01 | ELISA Kit DIY Materials for Mannose Binding Lectin (MBL) | Main materials for "Do It (ELISA Kit) Yourself". |