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Phosphate buffer solution (pH 8.6) 3404 immunoelectrophoresis method

NegotiableUpdate on 04/25
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Phosphate buffer solution (pH8.6) 3404 immunoelectrophoresis method: Operation method (for reference only) $r $n Inspection method Pour the agarose solution onto a horizontal glass plate of suitable size with a thickness of about 3mm, stand still, and after it is solidified into a uniform thin layer without bubbles, punch a hole at the top and bottom of 1/3 of the negative electrode of the agarose gel plate, with a hole diameter of 3mm and a hole spacing of 10-15mm. Add 10ul of test solution and 1 drop of bromophenol blue indicator solution to the measurement hole, and add 10ul of normal serum or plasma to the control hole (omitted).
Product Details

NamePhosphate buffer solution (pH 8.6) 3404 immunoelectrophoresis method

Specification: 500ml

Usage: Electrophoresis experiment, human white separation experiment

Acetate cellulose film electrophoresis experiment, etc

Storage conditions: Room temperature, 6 months

The immunoelectrophoresis experiment separates the test sample into various antigens in different bands through electrophoresis, and then performs biphasic immunodiffusion with the corresponding antibodies. When the ratio of the two is appropriate, a visible precipitation arc is formed. By comparing the position and shape of the precipitation arc with those generated by known standard antigens and antibodies, the composition and properties of the test sample can be analyzed.

Operation method (for reference only)

Inspection method Pour the agarose solution onto a horizontal glass plate of appropriate size with a thickness of about 3mm, stand still, and after it is solidified into a uniform thin layer without bubbles, punch a hole at the top and bottom of 1/3 of the negative pole of the agarose gel plate, with a hole diameter of 3mm and a hole spacing of 10-15mm. Add 10ul of test solution and 1 drop of bromophenol blue indicator solution to the measuring hole, and add 10ul of normal serum or plasma to the control hole (omitted).

Operation points

1. Solution pouring: Pour the agarose solution into a horizontal glass plate, ensuring a uniform thickness of 3mm. If the thickness is insufficient, it can be adjusted by adding small amounts multiple times.

2. Static solidification: Let it stand for about 30 minutes until the agarose is completely solidified, avoiding vibration or touch during this period to ensure the formation of a uniform thin layer without bubbles.

3. Follow up processing: After solidification, check whether the surface is flat and smooth. If there are bubbles, use a needle to puncture and squeeze out excess solution.


Precautions

If the temperature of the agarose solution is too high (over 45 ℃), it may cause prolonged solidification time or surface cracking. It is recommended to cool it to below 40 ℃ before pouring. The settling time should not exceed 4 hours, otherwise local solidification may occur, and it needs to be reheated for dissolution.

Phosphate buffer solution (pH 8.6) Pharmacopoeia 3404 Immunoelectrophoresis method