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Merck
CN

B6916

Bradford试剂

for 0.1-1.4 mg/ml protein

别名:

考马斯染料结合蛋白检测,蛋白染料试剂

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关于此项目

NACRES:
NA.32
UNSPSC Code:
12161500
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form

solution

storage temp.

2-8°C

Quality Level

General description

Bradford检测是把考马斯亮蓝G-250加入至蛋白溶液中。考马斯蓝染料可与碱性和芳香族氨基酸结合,从而在蛋白质测定过程中引起吸光值的迁移。

Application

Bradford试剂已用于测定总蛋白的浓度。

Features and Benefits

  • 该试剂为即用型。 无需混合或稀释。
  • 显色很快速。 仅需五分钟的孵育便能将样本在595 nm处进行读值。
  • 带有硫醇的还原性糖和还原性底物并不会干扰该试剂。
  • 试剂适用于微量(1-10 μg/ml)及标准(50-1400 μg/ml)的检测。
  • 可用于微孔板检测。
  • 低成本检测。

Legal Information

pictograms

Health hazardCorrosion

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Met. Corr. 1 - Skin Irrit. 2 - STOT SE 2

target_organs

Eyes,Central nervous system

flash_point_f

Not applicable

flash_point_c

Not applicable

存储类别

12 - Non Combustible Liquids


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sin-Jin Li et al.
Clinical nutrition (Edinburgh, Scotland), 36(3), 760-767 (2016-06-28)
The cellular mechanisms of obesity-induced cardiomyopathy are multiple and not completely elucidated. The objective of this study was to differentiate two obesity-associated cardiomyopathy miniature pig models: one with the metabolic syndrome (MetS), and one with a metabolically healthy obesity (MHO).
Rosenberg IM
Protein Analysis and Purification: Benchtop Techniques (2006)
Caleigh Mandel-Brehm et al.
Neurology, 93(5), e433-e444 (2019-07-05)
To identify molecular correlates of primary angiitis of the CNS (PACNS) through proteomic analysis of CSF from a biopsy-proven patient cohort. Using mass spectrometry, we quantitatively compared the CSF proteome of patients with biopsy-proven PACNS (n = 8) to CSF
Tracey Welham et al.
Journal of experimental botany, 60(12), 3353-3365 (2009-05-29)
Neutral/alkaline invertases are a subgroup, confined to plants and cyanobacteria, of a diverse family of enzymes. A family of seven closely-related genes, LjINV1-LjINV7, is described here and their expression in the model legume, Lotus japonicus, is examined. LjINV1 previously identified
Proteomic response of the biological control fungus Trichoderma atroviride to growth on the cell walls of Rhizoctonia solani.
Grinyer J et al.
Current Genetics, 47, 381-381 (2005)

商品

The field of proteomics is continually looking for new ways to investigate protein dynamics within complex biological samples. Recently, many researchers have begun to use RNA interference (RNAi) as a method of manipulating protein levels within their samples, but the ability to accurately determine these protein amounts remains a challenge. Fortunately, over the past decade, the field of proteomics has witnessed significant advances in the area of mass spectrometry. These advances, both in instrumentation and methodology, are providing researchers with sensitive assays for both identification and quantification of proteins within complex samples. This discussion will highlight some of these methodologies, namely the use of Multiple Reaction Monitoring (MRM) and Protein-AQUA.

实验方案

To determine protein content, the Warburg-Christian method refers to measuring protein samples at 280 nm using a spectrophotometer.

Rules and good practice in sample preparation for Western blot sample preparation from cell culture and tissue samples.

相关内容

Products for traditional and alternative protein quantitation techniques available, including BCA, Bradford, Lowry, and more.

蛋白定量方法、试剂和免疫测定技术可准确测定各类样品中的蛋白浓度。

Protein quantification methods, reagents, and immunoassay technology for accurately measuring the protein concentrations in a variety of samples.

We have developed a novel, high-binding capacity, antibodybased resin for the depletion of twenty high abundance proteins in human plasma. The technology is a significant improvement over existing kits that remove 2, 6, or 12 proteins.

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