Features | No danger of biohazards |
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No difference in lots | |
Suppression of non-specific adsorption | |
Stabilization of immobilized antibody | |
Stabilization of enzyme-antibody conjugate | |
Enhancement of aggregation reaction | |
Enhancement of enzyme-substrate reaction | |
Enhancement of accuracy | |
Reduction of CV value ([standard deviation] / [average] x 100) | |
Improvement of particle dispersiveness |
General Usage |
Can be supplied as 5 wt% aqueous solution
Do not use Biolipidure¢â directly, because it is not a buffer solution. |
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Can be used in ELISA, Western Blotting, Immuno-histochemistry. | |
¡Ø Dilute with a buffer solution.
It is recommended that the conc. of Biolipidure is used as 1.0 wt% - 0.01 wt%. |
Solid phase : 96-well plate (Maxisorp F96, Nunc) |
Immobilized antibody : anti (mouse IgG)IgG |
Antigen : non |
Enzyme-IgG conjugate : HRP-Anti (mouse IgG) IgG conjugate |
Substrate : o-phenylenediamine dihydrochloride Detection: 492 nm |
Experiment condition : | |
- | Immobilization of anti (mouse IgG)IgG |
- | Blocking by 0.1% (1 mg/mL) BIOLIPIDURE and 1 mg/mL BSA |
- | Dispensation of HRP-Anti (mouse IgG) IgG conjugate |
- | Dispensation of o-phenylenediamine dihydrochloride |
- | Measurement of absorbance at 492 nm |
Solid phase : 96-well plate (Maxisorp F96, Nunc) |
Immobilized antibody : anti (mouse IgG)IgG |
Antigen : mouse IgG |
Enzyme-IgG conjugate : HRP-Anti (mouse IgG) IgG conjugate |
Substrate : o-phenylenediamine dihydrochloride |
Detection : 492 nm |
Experiment condition : | |
- | Immobilization of anti (mouse IgG)IgG |
- | Blocking by by 0.1% BIOLIPIDURE and 0.1 % BSA |
- | Storage at 40 ¡Æ£Ã : 0, 4, 7, 14 and 20 day |
- | Dispensation of mouse IgG |
- | Dispensation of HRP-Anti (mouse IgG) IgG conjugate |
- | Dispensation of o-phenylenediamine dihydrochloride |
- | Measurement of absorbance at 492 nm |
Solid phase : 96-well plate (Maxisorp F96, Nunc) |
Immobilized antibody : anti (mouse IgG)IgG |
Antigen : mouse IgG |
Enzyme-IgG conjugate : HRP-Anti (mouse IgG) IgG conjugate |
Substrate : o-phenylenediamine dihydrochloride |
Detection : 492 nm |
Experiment condition : | |
- | Preparation of plate (immobilized antibody and reacted antigen) |
- | Dispensation of 1 % BIOLIPIDURE and BSA into HRP-IgG conjugate |
- | Storage at 25 ¡Æ£Ã: 0, 3, 7, 14, 24 and 37 day |
- | Dispensation of HRP-Anti (mouse IgG) IgG |
- | Dispensation of o-phenylenediamine dihydrochloride |
- | Measurement of absorbance at 492 nm |
Analysis : 0.8 mg/dL CRP using 7070 Auto Analyzer (HITACH) |
Measurement: latex turbidly immunoassay |
Experiment condition : | |
- | Dispensation of 1% BIOLIPIDURE, PEG and PVP into R1 reagent |
PEG : polyethylene glycol (Mw = 6,000) |
PVP : polyvinylpyrrolidone (Mw = 40,000) |
- Biolipidure¢â features - | |
- | No danger of biohazards and no difference in lots |
- | Improvement of stability, accuracy, reproducibility and sensitivity. |
- | Can be supplied as 5 wt% aqueous solution |
- Usage of Biolipidure¢â as a mobile phase - | |
#1 | Prepare the buffer solution including one wt% of Biolipidure. |
#2 | Dissolve the sample (For example; mucosa) in the above buffer. |
#3 | Put the diluted sample on the solid phase of immunochromatography. |
- Usage of Biolipidure¢â as a solid phase - | |
#1 | Prepare the solution of antibodies-conjugated gold colloids. |
#2 | Draw the line using the colloids solution on the solid phase of immunochromatography. |
#3 | Soak the solid phase in the buffer solution including one wt% of Biolipidure. |
#4 | Pick up the solid phase and dry it. You can get the solid phase blocked by Biolipidure. |