Protein Silver Stain Kit - 20 preps, high purity

Cat. No.: P665901

Descripción general

This reagent kit uses highly sensitive silver dye, which can be applied to protein staining of denatured and non denatured gels. It has the advantages of clear target bands, low background, and flexible control of operation time. In addition, this reagent kit has added a short-term sensitization step, which can significantly reduce the background and enhance the brightness of the target band.

P665901	Component	20 T	Storage
P665901A	Silver Stain Sensitizer (500×)	2×1 mL	RT
P665901B	Silver Stain Enhancer	3 mL	RT
P665901C	Silver Stain	2×250 mL	RT
P665901D	Silver Stain Developer	4×125 mL	RT

Matters needing attention
1. Please prepare 50 ml of fixed solution (ultrapure water: ethanol: acetic acid=6:3:1), 50 ml of eluent (10% ethanol), and 50 ml of termination solution (5% acetic acid) in advance.
2. Please use deionized water and clean glass or plastic containers during operation, and wear disposable gloves for operation.
The entire silver dyeing process needs to be carried out on a shaker, with a rotation speed of about 60 rpm.
4. Self prepared ethanol and glacial acetic acid are required.

Instructions for use
The dosage of each solution in the following operation steps takes the gel with a size of 8.5 × 5.5 cm and a thickness of 1.0 mm as an example. The gel is immersed in the solution completely, and is operated on a shaker, with a general dosage of 25 ml. For large gel, the dosage of each solution should be scaled up according to the gel volume. Please prepare 50 ml of fixed solution (ultrapure water: ethanol: glacial acetic acid=6:3:1), 50 ml of eluent (10% ethanol), and 50 ml of termination solution (5% glacial acetic acid) in advance.
1. Water washing: After electrophoresis is completed, wash the gel twice with ultrapure water for 5 minutes each time.
2. Fixation: Fix the gel twice with 25 ml of fixative solution for 15 minutes each time.
3. Elution: Wash the adhesive twice with eluent, each time for 5 minutes.
4. Water washing: Wash the glue twice with ultrapure water, each time for 5 minutes.
5. Sensitization: put the gel washed in the previous step into the silver dye sensitization working solution, incubate it accurately for 1 minute at room temperature, and then wash it with ultrapure water for three times, each time for 20 seconds. Preparation of silver staining sensitization working solution: Take 50 µ l Silver Stain Sensitivity (500 x) and add it to 25 ml of ultrapure water, mix well.
6. Silver staining: discard ultrapure water and incubate gel in silver staining working solution for 30 minutes. Preparation of silver staining working solution: Take 25ml Silver Stain and add 50 µ l Silver Stain Enhanced to mix well.
7. Water washing: Quickly wash the glue twice with ultrapure water, with each washing accurately controlled for 20 seconds.
8. Development: Immerse the washed gel in the developer immediately and incubate it at room temperature for 2-3 minutes until the protein strip is clear. Preparation of developer: Take 25ml Silver Stain Developer and add 30 µ l Silver Stain Enhanced to mix well. Attention: Within 30 seconds of development, protein bands begin to appear and continue to develop for 2-3 minutes. If the protein band appears lighter, the development time can be appropriately extended to 5 minutes or more.
9. Termination: After washing the developer on the gel with the termination solution, soak the gel in a new termination solution to react for 10 minutes.

Experimental images

Silver staining results of BSA protein samples after 10% SDS-PAGE gel electrophoresis
The molecular weight of BSA protein is about 66 kD, and the loading amounts from left to right are 50 ng, 10 ng, and 5 ng, respectively

Almacenamiento y envío

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal