SYPRO™ Ruby 蛋白质印迹染色
SYPRO™ Ruby 蛋白质印迹染色
SYPRO™ Ruby 蛋白质印迹染色
SYPRO™ Ruby 蛋白质印迹染色
Invitrogen™

SYPRO™ Ruby 蛋白质印迹染色

SYPRO Ruby 蛋白印迹染色是一种高灵敏度、即用型荧光染料,用于将蛋白转印至硝酸纤维素或 PVDF 膜,从而便于评估蛋白转印至印迹膜的效率并确定泳道是否均匀上样。与免疫染色(Western 印迹了解更多信息
Have Questions?
货号数量
S11791200 mL
货号 S11791
价格(CNY)
3,089.00
Online Exclusive
Ends: 31-Dec-2025
3,919.00
共减 830.00 (21%)
Each
添加至购物车
数量:
200 mL
请求批量或定制报价
价格(CNY)
3,089.00
Online Exclusive
Ends: 31-Dec-2025
3,919.00
共减 830.00 (21%)
Each
添加至购物车
SYPRO Ruby 蛋白印迹染色是一种高灵敏度、即用型荧光染料,用于将蛋白转印至硝酸纤维素或 PVDF 膜,从而便于评估蛋白转印至印迹膜的效率并确定泳道是否均匀上样。与免疫染色(Western 印迹)、微测序和质谱分析兼容。染色蛋白可使用蓝光 LED 或紫外光透射仪,或使用带适当过滤器或激光的成像设备进行观察。

比较所有荧光染料 ›
仅供科研使用。不可用于诊断程序。
规格
检测定位印迹检测
检测方法荧光
产品线SYPRO
产品类型蛋白印迹染料
数量200 mL
运输条件室温
靶标分子蛋白质
标签或染料SYPRO Ruby
Unit SizeEach
内容与储存
室温避光储存。

常见问题解答 (FAQ)

经过Pro-Q Diamond磷酸化蛋白质印迹膜染料染色的印迹膜,能否再使用SYPRO Ruby印迹膜染料染色以进行总蛋白检测?

可以。我们推荐在使用Pro-Q Diamond磷酸化蛋白质印迹膜染料染色后,再使用SYPRO Ruby印迹膜染料染色。

I have stained my blot with Pro-Q Diamond Phosphoprotein Blot Stain. Can I also stain the blot with SYPRO Ruby Blot Stain for total protein detection?

Yes. We recommend staining with SYPRO Ruby Blot Stain after staining with Pro-Q Diamond Phosphoprotein Blot Stain.

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

引用和文献 (10)

引用和文献
Abstract
Laser capture microdissection and protein microarray analysis of human non-small cell lung cancer: differential epidermal growth factor receptor (EGPR) phosphorylation events associated with mutated EGFR compared with wild type.
Authors:VanMeter AJ, Rodriguez AS, Bowman ED, Jen J, Harris CC, Deng J, Calvert VS, Silvestri A, Fredolini C, Chandhoke V, Petricoin EF, Liotta LA, Espina V,
Journal:Mol Cell Proteomics
PubMed ID:18687633
'Little is known about lung carcinoma epidermal growth factor (EGF) kinase pathway signaling within the context of the tissue microenvironment. We quantitatively profiled the phosphorylation and abundance of signal pathway proteins relevant to the EGF receptor within laser capture microdissected untreated, human non-small cell lung cancer (NSCLC) (n = 25) ... More
Novel observations of Thiobacterium, a sulfur-storing Gammaproteobacterium producing gelatinous mats.
Authors:Grünke S, Lichtschlag A, de Beer D, Kuypers M, Lösekann-Behrens T, Ramette A, Boetius A,
Journal:ISME J
PubMed ID:20220790
The genus Thiobacterium includes uncultivated rod-shaped microbes containing several spherical grains of elemental sulfur and forming conspicuous gelatinous mats. Owing to the fragility of mats and cells, their 16S ribosomal RNA genes have not been phylogenetically classified. This study examined the occurrence of Thiobacterium mats in three different sulfidic marine ... More
Herp, a new ubiquitin-like membrane protein induced by endoplasmic reticulum stress.
Authors:Kokame K, Agarwala KL, Kato H, Miyata T
Journal:J Biol Chem
PubMed ID:10922362
Hyperhomocysteinemia, a risk factor for vascular disease, injures endothelial cells through undefined mechanisms. We previously identified several homocysteine-responsive genes in cultured human vascular endothelial cells, including the endoplasmic reticulum (ER)-resident molecular chaperone GRP78/BiP. Here, we demonstrate that homocysteine induces the ER stress response and leads to the expression of a ... More
TrkB has a cell-autonomous role in the establishment of hippocampal Schaffer collateral synapses.
Authors:Luikart BW, Nef S, Virmani T, Lush ME, Liu Y, Kavalali ET, Parada LF
Journal:J Neurosci
PubMed ID:15829629
Neurotrophin signaling has been implicated in the processes of synapse formation and plasticity. To gain additional insight into the mechanism of BDNF and TrkB influence on synapse formation and synaptic plasticity, we generated a conditional knock-out for TrkB using the cre/loxp system. Using three different cre-expressing transgenic mice, three unique ... More
A thousand points of light: the application of fluorescence detection technologies to two-dimensional gel electrophoresis and proteomics.
Authors:Patton WF
Journal:Electrophoresis
PubMed ID:10786886
As proteomics evolves into a high-throughput technology for the study of global protein regulation, new demands are continually being placed upon protein visualization and quantitation methods. Chief among these are increased detection sensitivity, broad linear dynamic range and compatibility with modern methods of microchemical analyses. The limitations of conventional protein ... More