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Merck

PCG2012

Sigma-Aldrich

TruPAGE プレキャストゲル

4-20%, 10 x 8cm, 12-well

別名:

Precast Gels for SDS-PAGE, Precast Polyacrylamide Gels

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About This Item

UNSPSCコード:
41105300
NACRES:
NB.22

詳細

for use with Bio-Rad Mini-PROTEAN™ Tetra Cell, Mini-PROTEAN Dodeca™, Mini-PROTEAN II and 3 cells reverse device gasket to flat side

シェルフライフ

24 mo. at 2‑8 °C (from the date of manufacture)

包装

box of 10 ea

濃度

4-20% polyacrylamide

カセットW × L

10 cm × 8 cm

ゲル厚

1 mm

ウェルサイズ × 容積

12 wells × 35 μL

適合性

for use with Hoefer Mighty Small II and Tall Mighty Small (SE 260 and SE280)

保管温度

2-8°C

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特徴および利点

TruPAGE SDS-PAGE Precast Gels provide improved protein resolution, tear resistance, and an extended shelf-life. TruPAGE gels are formulated with Triethanolamine (TEA)-Tricine, featuring a neutral pH running environment that helps prevents protein modification during the course of the experiment.
The precast gels for SDS-PAGE come in two gel cassette sizes (10 x 10 cm and 10 x 8 cm) for increased equipment compatibility. TruPAGE gels have extra tall wells to prevent lane-to-lane overflow and come in two well formats (12-well and 17-well). TruPAGE gels are available in several different gel concentrations (10%, 12%, 4-8%, 4-12% and 4-20%) to provide desired resolution of proteins of any size. Please refer to the migration chart to select the appropriate precast gel and running buffer combination for your experimental needs. Only use TruPAGE formulated buffers when running TruPAGE gels to ensure optimal results and reproducibility. Please review the TruPAGE Technical Bulletin for buffer formulation recipes and general running guidelines.

  • Long Shelf Life - 2 years from the date of manufacture when stored properly.
  • High Performance - Extended full length resoling gels provides improved resolution.
  • Durable - Stronger than standard polyacrylamide gels, preventing tearing during post-electrophoresis processing.
  • Extra Tall Wells - Eliminate sample spill over and accommodate larger sample loading volumes with well teeth that protrude above the back plate of the gel cassette.
  • Excellent Compatibility - TruPAGE gels are compatible with the popular gel running equipment, including Sigma-Aldrich′s Dual Run Tank (Z741768) and other manufacturers like Life Technologies, Bio-Rad®, Lonza®, Hoefer®, CBS Scientific as well as others, allowing you to continue using the equipment you already own.
  • Fast - Run times as low as 30 minutes.
  • Great Value - Gels and buffers offer a cost-saving alternative without sacrificing performance and experimental integrity.
TruPAGE Precast Gels Migration Chart
There is no tape to remove. There is also no comb to remove, which prevents torn or bent wells. Instead, the cassettes lock well fingers in place.
TruPAGE Precast Gels 4-20% have been used to separate proteins through sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE), followed by Western blotting.

法的情報

Bio-Rad is a registered trademark of Bio-Rad Laboratories, Inc.
Hoefer is a registered trademark of Hoefer, Inc.
Lonza is a registered trademark of Lonza Group Ltd.
TruPAGE is a trademark of Sigma-Aldrich Co. LLC

保管分類コード

12 - Non Combustible Liquids

WGK

WGK 2

引火点(°F)

Not applicable

引火点(℃)

Not applicable


適用法令

試験研究用途を考慮した関連法令を主に挙げております。化学物質以外については、一部の情報のみ提供しています。 製品を安全かつ合法的に使用することは、使用者の義務です。最新情報により修正される場合があります。WEBの反映には時間を要することがあるため、適宜SDSをご参照ください。

毒物及び劇物取締法

劇物

Jan Code

PCG2012-2EA:4548174010570
PCG2012-10EA:4548174010563


試験成績書(COA)

製品のロット番号・バッチ番号を入力して、試験成績書(COA) を検索できます。ロット番号・バッチ番号は、製品ラベルに「Lot」または「Batch」に続いて記載されています。

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Registered report: Transcriptional amplification in tumor cells with elevated c-Myc.
Blum D, et al.
eLife, 4, e04024-e04024 (2015)
Amanda L Wong et al.
Methods (San Diego, Calif.), 184, 102-111 (2020-02-06)
The development of universal, broadly applicable methods for histone extraction from animal cells and tissues has unlocked the ability to compare these epigenetic-influencing proteins across tissue types, healthy and diseased states, and cancerous versus normal cells. However, for plants and
Camila Yattah et al.
Neurochemical research, 45(3), 606-619 (2020-02-06)
Differentiation of oligodendrocytes (OL) from progenitor cells (OPC) is the result of a unique program of gene expression, which is further regulated by the formation of topological domains of association with the nuclear lamina. In this study, we show that

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