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Invitrogen™ ZOOM™ IPG Strips pH 9-12
Description
Requires
ZOOM IPGRunner System
- First dimension separation, isoelectric focusing (IEF), is complete in less than three hours
- The mini-gel design of the system is easy to handle, eliminates mineral oil overlays, and allows processing of up to 12 samples at once for high-throughput usage
- Strips are 7cm long and contain a thin layer of polyacrylamide gel that includes a fixed pH gradient
- Each strip is clearly labeled with a unique identifying number, pH range, and orientation marks
- Strips are supplied attached to a tri-fold card for easy access and removal
2D Gel Electrophoresis, IsoElectric Focusing, Protein Gel Electrophoresis, Protein Sample Fractionation, Protein Sample Preparation and Protein Purification, Proteins, Expression, Isolation and Analysis
Order Info
Shipping Condition: Dry Ice
Specifications
Specifications
| Content And Storage | The ZOOM™ IPGRunner™ Mini-Cell includes the ZOOM™ IPGRunner™ Buffer Core and Lid, Gel Tension Wedge, Buffer Dam, and the Mini- Cell chamber. The ZOOM™ IPGRunner™ Combo Kit includes the ZOOM™ IPGRunner™ Mini-Cell, electrode wicks, sealing tape, 10 ZOOM™ IPGRunner™ Cassettes, and 12 ZOOM™ Strips, pH 3-10 NL. The ZOOM™ IPGRunner™ Retrofit Kit for XCell SureLock™ Mini-Cell includes the ZOOM™ IPGRunner™ Buffer Core and Lid. The ZOOM™ IPGRunner™ Cassettes include electrode wicks and sealing tape. |
| Gel Size | Mini |
| pH Range | 9.0 - 12.0 |
| Quantity | 12 strips |
| Shipping Condition | Dry Ice |
| Product Line | ZOOM |
| Product Type | IPG Strip |
| For Use With (Equipment) | XCell SureLock Mini-Cell |
Frequently Asked Questions (FAQs)
1) Trim excess plastic from IPG strip
2) Equilibrate IPG strip for 2 x 15 min in 5 mL of the appropriate buffer (Use NuPAGE sample buffer for NuPAGE ZOOM gels and Tris Glycine ZOOM gels). Equilibration buffer: 1X NuPAGE sample buffer, 50 mM DTT.
3) Place equilibrated IPG strip in large well of ZOOM gel. Seal the strip in place with an agarose (0.5%) overlay.
4) Load molecular weight markers in small well of ZOOM gel.
Variations: To alkylate the proteins after reducing them, prior to separation on ZOOM gels: 1) Incubate IPG strip for 15 min in equilibration buffer 2) Transfer strip to Equilibration Buffer containing 125 mM iodoacetamide and lacking reducing agent. Incubate an additional 15 min. To denature the proteins with urea after IEF: 6 M urea can be added to Equilibration Buffer, if desired.
Incubating ZOOM Strips in NuPAGE LDS Sample Buffer equilibrates the strips in SDS buffer and prepares the strips for 2D SDS-PAGE.
We recommend using the NuPAGE LDS Sample Buffer containing 50 mM DTT (NuPAGE Sample Reducing Agent) with NuPAGE Invitrogen 4-12% Bis-Tris ZOOM Gels and Invitrogen 4-20% Tris-Glycine ZOOM Gels. You need 5-15 mL of buffer per equilibration tray. For alkylation, we recommend incubating the strips in 125 mM Alkylating Solution (prepared by dissolving 232 mg of fresh iodoacetamide in 10 mL of 1X NuPAGE LDS Sample Buffer).
*The rehydration buffer is the best extraction buffer for IPG strips.
*The ionic strength of the buffer should be low; e.g., PBS will not work because the ionic strength is pretty high (150-250 mM), depending on salt and other ionic components.
*Proteins can be precipitated and re-suspended in rehydration buffer; use acetone for precipitation.
Our proprietary formulation for our ZOOM Strips has been tested and been shown to allow for a 60-90 minute rapid rehydration step. It is not necessary to go overnight, although for convenience, you still can rehydrate for 8-16 hours. For the one hour rehydration, it is important not to exceed the 140 µL sample volume. The proteins get in very quickly but the liquid may be left behind. If rehydrating overnight, use the 155 µL sample volume.
We do not recommend heating protein samples containing urea over 37 degrees C as elevated temperatures cause urea to hydrolyze to isocyanate, which modifies proteins by carbamylation.
For Research Use Only. Not for use in diagnostic procedures.