Comparison

Gelatin Zymography Kit (ATTO type: wide thick plates)

Item no. PMC-AK45
Manufacturer Cosmobio
Amount 1 Kit
Category
Type Kit
Specific against other
ECLASS 10.1 32161090
ECLASS 11.0 32161090
UNSPSC 41116126
Available
Manufacturer - Category
Research Area/Cell Biology/Extracellular Matrix/Zymography; Assays/Extracellular Matrix/Zymography; Assays/Zymography
Maker
PMC
Description
Zymography Kit provides an easy system of the electrophoresis for zymography. This product is used for detecting ProMMP-2, MMP-2 and ProMMP-9 in blood, body fluid, secretion, cell lysate, cell culture medium, and other samples.
[Cautions: This product has a short expiration date (less than 3 months). Please use it after arrival as soon as possible.
Protocol: 1. Load 100-150 ml of Electrophoresis Buffer to the lower chamber (anode). Refer to the instruction manual ofyour electrophoresis tank/chamber to know appropriate volume of the buffer.
2. Take out the comb on precast gel carefully and set the gel to electrophoresis chamber. The side of sample holes should be set on the upper side. If the sample holes aredisturbed, fix them up with needle etc.
3. Load around 100 ml of Electrophoresis Buffer to the upper chamber (cathode).
4. Mixsamples with equivalent volume of sample preparation buffer. Incubate for 15 minutes at Room Temperature. (Do NOT heat thesamples.)
*MMP markers can be used without sample preparation buffer.
5. Apply the samples and MMP markers to gel plate.
6.Run electrophoresis at 15 mA constant current. (If you use 2 gels, set the current at 30 mA)
7. After the run is completed, turn off the electrophoresis chamber, and take out the gel plate from the chamber.
8. Remove the upper glass plate of thegel plate and peel off the gel carefully with a spatula.
9. Put the gel in the tray with 200 ml of Washing Buffer. Incubate withshaking at Room Temperature.
10. Put the gel in the container with 50 ml of Reaction Buffer and seal up the container. Incubate the gel in the container in incubator at 37°C for 20-40 hrs (Lower enzyme concentration needs longer reaction time.)
11. After enzymatic reaction, put the gel in the container with Staining solution. Incubate for 30 minutes at Room Temperature to stain protein.
12. Put the gel in the container with De-staining solution. And incubate for 30 minutes to several hourstode-stain.

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Amount: 1 Kit
Available: In stock
available

Compare

Add to wishlist

Get an offer

Request delivery time

Ask a technical question

Submit a bulk request

Questions about this Product?
 
Close