Determine the necessary mass, volume, or concentration for preparing a solution.
for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
The core of the Blood-Brain Barrier (BBB) Permeability Assay Kit lies in using spectrophotometry to detect the concentration of substances that have penetrated the simulated blood-brain barrier. It features simple operation and low cost, making it suitable for rapid screening. No fluorescent labeling or radioactive probes are required; instead, it relies on the inherent light absorption properties of the substances themselves (or supporting chromogenic reagents). It has a low operational threshold and uses widely available equipment (a standard laboratory spectrophotometer is sufficient).
| B1506000 | Components | 50T | Storage |
| B1506000A | Standard Substance A | 2 mL | RT. Store in the dark. |
| B1506000B | Standard Substance B | 2 mL | RT. Store in the dark. |
| B1506000C | Standard Substance C | 2 mL | RT. Store in the dark. |
| B1506000D | Standard Substance D | 2 mL | RT. Store in the dark. |
| B1506000E | Standard Substance E | 2 mL | RT. Store in the dark. |
| B1506000F | Staining Solution | 10 mL | RT |
| B1506000G | Isolation Solution | 50 mL | RT |
| B1506000H | PBS | 1 L | RT |
Self-Prepared Consumables and Reagents:
Syringe
Tissue Homogenizer
Operating Steps (for reference only):
a. Take the treated experimental animals (using mice as an example). Intravenously inject 1–200 μl of staining solution (No. F). Within a few seconds to 1 minute, the eyes and skin of the mice will turn blue. Sacrifice the mice after 0.5–1 hour and collect the target brain tissue.
b. Place the brain tissue in a 1.5 ml centrifuge tube, add 1 ml of PBS, quickly homogenize the brain tissue using a tissue homogenizer, and centrifuge at 1000×g for 10 minutes at 4°C.
c. Take the supernatant, add an equal volume of separation solution (No. G), mix well, and incubate at 4°C for 18–24 hours.
d. Centrifuge at 2000×g for 15 minutes at 4°C.
e. Take an appropriate amount of the above solution and dilute it 10-fold. Take 1 ml of the diluted solution and measure the absorbance (OD value) at 620 nm using a spectrophotometer or microplate reader. Meanwhile, determine the OD values of standards A–E, plot a standard curve, and calculate the content of the staining solution in the test samples based on the standard curve.
Measured Values by the Company's Spectrophotometer:
| B1506000 | Standard Substance A | Standard Substance B | Standard Substance C | Standard Substance D | Standard Substance E |
Concentration | 39.062mM | 9.766mM | 2.441mM | 0.610mM | 0.152mM |
OD Value | 1.036 | 0.631 | 0.234 | 0.116 | 0.087 |
(Only relative changes in permeability can be observed, absolute quantification is not possible)
Precautions:
1. In the blood-brain barrier permeability experiment, the injection volume of the staining solution should be adjusted according to the type of animal and the animal's weight.
2. A low-temperature refrigerated centrifuge should be used for centrifugation.
3. For your safety and health, please wear a lab coat and disposable gloves during operation.
Comprehensive hazard, handling, storage, and regulatory compliance document.
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| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Mar 11, 2026 | B1506000 |
| Sensitivity | Light-sensitive |
|---|