NuPAGE™ LDS Sample Buffer (4X)
NuPAGE™ LDS Sample Buffer (4X)
Invitrogen™

NuPAGE™ LDS Sample Buffer (4X)

NuPAGE LDSサンプルバッファー(4X)は、Bis-TrisゲルまたはTris-Acetateゲルを用いて変性ゲル電気泳動を行う際にタンパク質サンプルを調製するために使用します。リチウムドデシル硫酸塩(pH 8.4)が含まれており、還元剤の活性を最大限に高めることができます詳細を見る
製品番号(カタログ番号)数量
NP000710 mL
NP0008250 mL
製品番号(カタログ番号) NP0007
価格(JPY)
4,700
Each
お問い合わせください ›
数量:
10 mL
NuPAGE LDSサンプルバッファー(4X)は、Bis-TrisゲルまたはTris-Acetateゲルを用いて変性ゲル電気泳動を行う際にタンパク質サンプルを調製するために使用します。リチウムドデシル硫酸塩(pH 8.4)が含まれており、還元剤の活性を最大限に高めることができます。

SDS-PAGEに使用可能なすべてのバッファーと試薬の一覧

NuPAGE LDSサンプルバッファーは、トラッキング色素としてブロモフェノールブルーではなくクマシーG250とフェノールレッドを含有しています。クマシーG250は、MESとMOPS SDSの両方の泳動バッファーでシャープな色素フロントを提供し、ブロモフェノールブルーよりも移動イオンフロントにはるかに近い位置に移動します。ブロモフェノールブルーの泳動は、MES SDS泳動バッファーでのパプチドより遅くなります。これにより、小さなペプチドはゲルから泳動しません。

使用法:最適な結果を得るために、70℃で10分間、1Xの希釈液(還元または非還元)でサンプルを加熱します。

注:NuPAGE LDSサンプルバッファーは、使用前に室温(25℃)に戻してください。これは、一般的なサンプルバッファーに含まれているSDSと比べて2倍の量のLDSを含む高粘性かつ高濃度の溶液です。また、NuPAGE LDSサンプルバッファーにはグリセロールも高濃度で含まれています。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
バッファーサンプルローディングバッファー
濃度4倍
ゲル適合性NuPAGE™ゲル
製品ラインNuPAGE
製品タイプLDSサンプルバッファー
数量10 mL
出荷条件室温またはウェットアイスでの出荷
ゲルタイプNuPAGEゲル
Unit SizeEach
組成および保存条件
SERVAブルーG250およびフェノールレッドを使用したpH 8.5リチウムドデシル硫酸塩(LDS)を含むサンプルバッファー(4X)。

保管温度4℃∼25℃。

よくあるご質問(FAQ)

Can I prepare my protein sample with the reducing agent and store it for future use?

DTT is not stable, so it must be added and the reduction performed just prior to loading your samples.

Find additional tips, troubleshooting help, and resources within our Protein Gel 1D Electrophoresis Support Center.

My LDS or SDS sample buffer precipitates when stored at 4 degrees C. Can I warm it up? Can I store it at room temperature?

Precipitation of the LDS or SDS at 4 degrees C is normal. Bring the buffer to room temperature and mix until the LDS/SDS goes into solution. If you do not want to wait for it to dissolve, you can store the sample buffer at room temperature.

Find additional tips, troubleshooting help, and resources within our Protein Gel 1D Electrophoresis Support Center.

How are Bolt gels different than NuPAGE gels?

While they are both Bis-Tris based gels, the chemistries are very different since Bolt gels are optimized for western blotting. Another key difference is the wedge well design of the Bolt gels, which allows larger sample volumes to be loaded.

Find additional tips, troubleshooting help, and resources within our Protein Gel 1D Electrophoresis Support Center.

What is the advantage of NuPAGE Gels over regular Tris-Glycine gels?

The neutral operating pH of the NuPAGE Gels and buffers provides following advantages over the Laemmli system:
-Longer shelf life of 8-12 months due to improved gel stability
-Improved protein stability during electrophoresis at neutral pH resulting in sharper band resolution and accurate results (Moos et al, 1998)
-Complete reduction of disulfides under mild heating conditions (70 degrees C for 10 min) and absence of cleavage of asp-pro bonds using the NuPAGE LDS Sample buffer (pH > 7.0 at 70 degrees C)
-Reduced state of the proteins maintained during electrophoresis and blotting of the proteins by the NuPAGE Antioxidant
Please refer to the following paper: Moos M Jr, Nguyen NY, Liu TY (1988) Reproducible High Yield Sequencing of Proteins Electrophoretically Separated and Transferred to an Inert Support. J Biol Chem 263:6005-6008.

Find additional tips, troubleshooting help, and resources within our Protein Gel 1D Electrophoresis Support Center.

What is the composition of the NuPAGE LDS Sample Buffer and what is the recipe for the 4X formulation?

The composition of the 1X NuPAGE LDS Sample Buffer is as follows:

141 mM Tris base
106 mM Tris HCl
2% LDS
10% Glycerol
0.51 mM EDTA
0.22 mM SERVA Blue G
0.175 mM Phenol Red
pH 8.5


To prepare 10 mL of 4 X NuPAGE LDS Sample Buffer, dissolve the following reagents to 8 mL ultrapure water:

Tris HCl 0.666 g
Tris Base 0.682 g
LDS 0.800 g
EDTA 0.006 g
Glycerol 4 g
SERVA Blue G (1 solution) 0.75 mL
Phenol Red (1 solution) 0.25 mL

Mix well and adjust the volume to 10 mL with ultrapure water. Store at +4. The buffer is stable for 6 months when stored at +4°C.

Find additional tips, troubleshooting help, and resources within our Protein Gel 1D Electrophoresis Support Center.

引用および参考文献 (9)

引用および参考文献
Abstract
Characterization of four murine homologs of the human ov-serpin monocyte neutrophil elastase inhibitor MNEI (SERPINB1).
Authors: Benarafa Charaf; Cooley Jessica; Zeng Weilan; Bird Phillip I; Remold-O'Donnell Eileen;
Journal:J Biol Chem
PubMed ID:12189154
'The human ov-serpin monocyte neutrophil elastase inhibitor (MNEI) is encoded by a single gene SERPINB1. It is a highly efficient inhibitor of neutrophil granule proteases. Four murine genes with high sequence identity with MNEI were identified and fully sequenced, and these were named EIA, EIB, EIC, and EID. EIA, EIB ... More
Novel Modulation of Neuronal Nicotinic Acetylcholine Receptors by Association with the Endogenous Prototoxin lynx1.
Authors: Ibañez-Tallon Inés; Miwa Julie M; Wang Hai Long; Adams Niels C; Crabtree Gregg W; Sine Steven M; Heintz Nathaniel;
Journal:Neuron
PubMed ID:11906696
We previously identified lynx1 as a neuronal membrane molecule related to snake alpha-neurotoxins able to modulate nAChRs. Here, we show that lynx1 colocalizes with nAChRs on CNS neurons and physically associates with nAChRs. Single-channel recordings show that lynx1 promotes the largest of three current amplitudes elicited by ACh through alpha(4)beta(2) ... More
Apolipoprotein A-I is a selective target for myeloperoxidase-catalyzed oxidation and functional impairment in subjects with cardiovascular disease.
Authors:Zheng L, Nukuna B, Brennan ML, Sun M, Goormastic M, Settle M, Schmitt D, Fu X, Thomson L, Fox PL, Ischiropoulos H, Smith JD, Kinter M, Hazen SL,
Journal:J Clin Invest
PubMed ID:15314690
In recent studies we demonstrated that systemic levels of protein-bound nitrotyrosine (NO(2)Tyr) and myeloperoxidase (MPO), a protein that catalyzes generation of nitrating oxidants, serve as independent predictors of atherosclerotic risk, burden, and incident cardiac events. We now show both that apolipoprotein A-I (apoA-I), the primary protein constituent of HDL, is ... More
In vivo functional assay of a recombinant aquaporin in Pichia pastoris.
Authors:Daniels MJ, Wood MR, Yeager M,
Journal:Appl Environ Microbiol
PubMed ID:16461705
The water channel protein PvTIP3;1 (alpha-TIP) is a member of the major intrinsic protein (MIP) membrane channel family. We overexpressed this eukaryotic aquaporin in the methylotrophic yeast Pichia pastoris, and immunogold labeling of cellular cryosections showed that the protein accumulated in the plasma membrane, as well as vacuolar and other ... More
Spermidine but not spermine is essential for hypusine biosynthesis and growth in Saccharomyces cerevisiae: Spermine is converted to spermidine in vivo by the FMS1-amine oxidase.
Authors:Chattopadhyay MK, Tabor CW, Tabor H,
Journal:Proc Natl Acad Sci U S A
PubMed ID:14617780
In our earlier work we showed that either spermidine or spermine could support the growth of spe2Delta or spe3Delta polyamine-requiring mutants, but it was unclear whether the cells had a specific requirement for either of these amines. In the current work, we demonstrate that spermidine is specifically required for the ... More