Nitrocellulose/Filter Paper Sandwiches, 0.45 μm, 8.6 x 13.5 cm

Nitrocellulose/Filter Paper Sandwiches, 0.45 μm, are high-quality membranes ideal for blotting proteins and nucleic acids. The 0.45-μm pore size is자세히 알아보기

카탈로그 번호	수량
LC2006	16 membrane/filter paper sandwiches

카탈로그 번호 LC2006

제품 가격(KRW)

413,000

카트에 추가하기

16 membrane/filter paper sandwiches

제품 가격(KRW)

413,000

카트에 추가하기

Nitrocellulose/Filter Paper Sandwiches, 0.45 μm, are high-quality membranes ideal for blotting proteins and nucleic acids. The 0.45-μm pore size is ideal for the transfer of most proteins (>20 kDa) and nucleic acids (>300 bp). The included extra-thick absorbent blotting paper (2.5 mm) accommodates blotting set-up using semi-dry transfer apparatuses.

See all membranes and filter papers ›

Features:
• Membrane: 100% pure nitrocellulose
• Filter paper thickness: 2.5 mm
• Binding capacity: ∼80 μg/cm² of proteins
• Binding interactions: hydrophobic and electrostatic
• Compatibility: compatible with commonly used transfer conditions and detection methods such as staining, immunodetection, chemiluminescence, fluorescence, and radiolabeling
• Supplied in a pre-cut, pre-assembled membrane/filter paper sandwich

For Research Use Only. Not for use in diagnostic procedures.

설명Nitrocellulose/Filter Paper Sandwich, 0.45μm pore size

수량16 membrane/filter paper sandwiches

배송 조건Room Temperature

Dimensions (LxW)8.6 cm x 13.5 cm

형식Sandwich

길이(미터법)13.5 cm

물질Nitrocellulose

기공 크기0.45 μm

제품라인Novex

두께2.5 mm

폭(미터법)8.6 cm

Unit SizeEach

구성 및 보관

Store at room temperature.

자주 묻는 질문(FAQ)

How should nitrocellulose be treated prior to transferring proteins?

Prewet the nitrocellulose membrane in distilled water or in 1X transfer buffer for 5 min with gentle shaking. This is to prevent any dry spots in the membrane that may interfere with transfer.

Find additional tips, troubleshooting help, and resources within our Protein Electrophoresis and Western Blotting Support Center.

How can I store, strip, and reuse my western blot?

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.

Find additional tips, troubleshooting help, and resources within our Protein Assays and Analysis Support Center.