NativePAGE™ Bis-Tris Mini Protein Gels, 4 to 16%, 1.0 mm
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Attention: BN2111BX10 is the equivalent SKU for BN1002BOX. Please contact Technical Support with any questions.
NativePAGE™ Bis-Tris Mini Protein Gels, 4 to 16%, 1.0 mm
Invitrogen™

NativePAGE™ Bis-Tris Mini Protein Gels, 4 to 16%, 1.0 mm

Invitrogen NativePAGE Bis-Trisゲルシステム は、プレキャストポリアクリルアミドミニゲルシステムで、天然タンパク質およびタンパク質複合体の高感度かつ高分解能分析を行い、分子量の推定や純度の評価を行います。
製品番号(カタログ番号)ウェル
BN2111BX1010ウェル
BN2112BX1015ウェル
製品番号(カタログ番号) BN2111BX10
価格(JPY)
-
お問い合わせください ›
ウェル:
10ウェル
Invitrogen NativePAGE Bis-Tris Protein gels are precast polyacrylamide mini-gels that provides sensitive, high-resolution analysis of native proteins and protein complexes for molecular mass estimations and assessment of purity. They are based on the blue native polyacrylamide gel electrophoresis (BN PAGE) technique developed by Schägger and von Jagow, which overcomes the limitations of traditional native electrophoresis by providing a near-neutral operating pH and detergent compatibility.

Invitrogen NativePAGE Bis-Tris Protein gels are precast polyacrylamide mini-gels that provides sensitive, high-resolution analysis of native proteins and protein complexes for molecular mass estimations and assessment of purity. They are based on the blue native polyacrylamide gel electrophoresis (BN PAGE) technique developed by Schägger and von Jagow, which overcomes the limitations of traditional native electrophoresis by providing a near-neutral operating pH and detergent compatibility.

Features of the NativePAGE Bis-Tris Protein gels include:

  • Wide molecular weight resolving range of 15–10,000 kDa
  • Neutral-pH separation, which better preserves the native state of protein complexes
  • Resolution of all proteins regardless of their isoelectric point (pI)
  • Ability to analyze membrane-protein complexes in their native conformations
  • Ability to obtain better resolution than with traditional tris-glycine native electrophoresis

How NativePAGE Bis-Tris Protein gels work

In SDS-PAGE, SDS functions as a charge-shift molecule that denatures proteins by conferring on them a net negative charge and enables proteins to migrate towards the anode. BN PAGE uses Coomassie G-250 as the charge-shift molecule, which binds to proteins and confers a net negative charge while maintaining the proteins in their nondenatured, native state. The near-neutral pH of the NativePAGE Bis-Tris Protein gels provides maximum stability of both the proteins and the gel matrix, resulting in a highly sensitive method for analysis of native membrane-protein complexes and offering superior band resolution over traditional Tris-glycine gel systems.

For transferring proteins to a membrane, we recommend using NuPAGE transfer buffers for traditional wet transfer and PVDF membranes. NuPAGE transfer buffers maintain the neutral pH environment established during electrophoresis. Nitrocellulose membranes are not compatible for blotting since the membrane will bind the Coomassie G-250 dye very tightly. Alternatively, rapid semi-dry transfer can be done using the Power Blotter (Cat. No. PB0013) or rapid dry transfer using the iBlot 3 Gel Transfer Device (IB31001) using PVDF membranes.

研究用にのみ使用できます。
仕様
使用対象 (装置)Mini Gel Tank
Gel Thickness1.0 mm
長さ(メートル法)8 cm
分離モード分子量
数量10ゲル/箱
サンプル充填量Up to 25 μL
品質保持期間8 Months
出荷条件Wet Ice
幅(メートル法)8 cm
ゲル濃度4 ∼ 16%
ゲルサイズミニ
ゲルタイプBis-Tris
製品ラインNativePAGE
分離範囲15 to 10,000 kDa
分離タイプ天然
ウェル10ウェル
Unit SizeEach
組成および保存条件
Store at 2°C to 8°C. Do not freeze.

よくあるご質問(FAQ)

Are NativePAGE gels and buffers compatible with Mini Gel tank?

Yes, NativePAGE gels are compatible with our Mini Gel tank, however there is a small variation from the original protocol.

The following protocol are for using NativePage gels with the Mini Gel Tank depending on if you are also performing a western transfer or not:
If you are NOT performing a western transfer:
1. Prepare 250 mL of each buffer (Anode and Dark Blue Cathode) per gel
2. After inserting a loaded NativePAGE gel into the Mini Gel Tank and pulling the clamp forward, fill the front cathode buffer chamber to the Fill Line with Dark Blue Cathode Buffer (~200 mL per gel)
3. Add 220 mL of Anode Buffer to the back anode buffer chamber for that gel. Start the gel run

If you are performing a western transfer:
1. Prepare 250 mL of Dark Blue Cathode Buffer, 250 mL of Light Blue Cathode Buffer, and 500 mL of Anode Buffer per gel
2. After inserting a loaded NativePAGE gel into the Mini Gel Tank and pulling the clamp forward, fill the front cathode buffer chamber to the Fill Line with Dark Blue Cathode Buffer (~200 mL per gel
3. Add 220 mL of Anode Buffer to the back anode buffer chamber for that gel
4. Start the gel run; pause the run after the dark blue dye has run ~1/3 of the way through gel
a. Pour out the buffers from the Mini Gel Tank
b. Refill the back anode buffer chamber with 220 mL of Anode Buffer per gel
c. Fill the front cathode buffer chamber to the Fill Line with Light Blue Cathode Buffer (~200 mL per gel)
5. Resume the gel run

Find additional tips, troubleshooting help, and resources within our Protein Biology Support Centers .