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Invitrogen™ Power Blotter Pre-cut Membranes and Filters, nitrocellulose, regular size
Description
Includes
The pre-cut membranes and filters come with 20 sheets of nitrocellulose and 80 sheets of absorbant blotting paper (0.85mm thickness)
The Invitrogen Power Blotter Pre-cut Membranes and Filters are designed for transferring proteins from gels using the Invitrogen Power Blotter System.
Features:
- Membranes and filters allow for high efficiency semi-dry transfer of proteins in less than 10 minutes when combined with the Power Blotter 1-Step Transfer Buffer
- 100% pure nitrocellulose membrane (0.2 μM pore size) with high surface area and excellent uniformity provides high-quality transfers.
- Nitrocellulose is a popular binding matrix for western blotting because of its high affinity for proteins and compatibility with a variety of detection methods such as chemiluminescence, chromogenic, and fluorescence.
- 209 μg/cm2 protein binding affinity
- Blocks easily produces very low background in chemiluminescent and fluorescent western blotting
- Convenient— Pre-cut sheets are ready to use, meaning no need to cut your own membranes, minimizing damage and contamination
- Validated – When combined, membrane and filter provide the thickness and buffer capacity needed for optimal performance
Specifications
Specifications
| Length (Metric) | 13 cm |
| Width (Metric) | 8.5 cm |
| Quantity | 20 stacks |
| Format | Transfer Stack |
| Material | Nitrocellulose |
| Pore Size | 0.2 μm |
| Content And Storage | 20 regular-size transfer stacks (13 cm x 8.3 cm) composed of 20 sheets of nitrocellulose and 80 sheets of filter paper (0.85 mm thickness) |
| Shipping Condition | Room Temperature |
| Dimensions (LxW) | Regular, 13 cm x 8.5 cm |
| Thickness | 0.85 mm |
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Frequently Asked Questions (FAQs)
For nitrocellulose or PVDF membrane following Western blot detection using a chemiluminescent or fluorescent substrate system: Following transfer, air dry the membrane and place in an envelope, preferably on top of a supported surface to keep the membrane flat. The blot can be stored indefinitely at -80 degrees C. When ready to reprobe, prewet the PVDF blot with alcohol for a few seconds, followed by a few rinses with pure water to reduce the alcohol concentration. Then proceed as normal with blocking step.
FOR STRIPPING/REPROBING OF MEMBRANES:
Harsh protocol (see NOTE below for modifications)
1) Submerge the membrane in stripping buffer (100 mM BME, 2% SDS, 62.5 mM Tris-HCl, pH 6.7) and incubate at 50 degrees C for 30 min with occasional agitation. If more stringent conditions necessary, incubate at 70 degrees C.
2) Wash 2 x 10 min in TBS-T/PBS-T at room temperature.
3) Block the membrane by immersing in 5% blocking reagent TBS-T or PBS-T for 1 hr at room temperature.
4) Immunodetection
NOTE: Often you don't need such harsh conditions to remove antibodies from their proteins. The stringency of one or several of the variables can be decreased: lower the temperature, decrease the time, less BME, less SDS, etc. An especially mild but still often effective stripping protocol is lower pH incubation. Example: pH 2.0 Tris 50-100 mM, 30-60 min incubation (you may do two incubations if you wish). Then rinse and block as usual. If you do not wish to re-use the membrane immediately after stripping, you can store the membrane in plastic wrap (wet, you do not want it to dry out). Another simple, mild stripping buffer is 0.1 M glycine•HCl (pH 2.5-3.0), incubation 30 min to 2 hrs room temperature or 37 degrees C, depending on the antibody.
The Power Blotter System (Cat. No. PB0012) comes with the Power Blotter Station (Cat. No. PB0010) plus Power Blotter Cassette (Cat. No. PB0002). The Power Blotter System can transfer one midi or up to two mini gels at the same time. The Power Blotter XL System (Cat. No. PB0013) on the other hand comes with the Power Blotter Station (Cat. No. PB0010) plus Power Blotter XL Cassette (Cat. No. PB0003). The Power Blotter XL System can transfer up to two midi or four mini gels at the same time.
Even though the Power Blotter System/Power Blotter XL System does not have the staining program, this can be introduced. Please see the user guide for our Pierce Mini/Midi Gel Power Staining Kit (https://assets.thermofisher.com/TFS-Assets/LSG/manuals/MAN0017799_22839_22840_powerstain_midi_minigel_UG.pdf) for how to create a Custom Staining Method.
The top (cathode) is stainless steel and the bottom (anode) is platinum-coated stainless steel.
Yes, you may purchase the Universal Cable Kit (Cat. No. 4377117).
Safety and Handling
For Research Use Only. Not for use in diagnostic procedures.
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