跳转至内容
Merck
CN

T8387

Thiopropyl–Sepharose 6B

lyophilized powder

别名:

Thiopropyl−activated–Agarose

登录 查看组织和合同定价。

选择尺寸

变更视图

关于此项目

化学文摘社编号:
UNSPSC Code:
13111000
NACRES:
NA.56
MDL number:
技术服务
需要帮助?我们经验丰富的科学家团队随时乐意为您服务。
让我们为您提供帮助


form

lyophilized powder

extent of labeling

18-31 μmol per mL

matrix active group

hydroxypropyl 2-pyridyl disulfide

swelling

1 g swells to 4-5 mL gel

storage temp.

2-8°C

Application

Thiopropyl Sepharose 6B is used in protein chromatography, affinity chromatography and hydrophobic interactions. Thiopropyl Sepharose 6B has been used for the removal of inhibitors from PCR extracts from evidence collected for law enforcement murder investigations. Thiopropyl Sepharose 6B has also been used to describe a method for the investigation of functional properties of distinct domains of viral thiol proteins, including the influenza virus membrane M1 protein.

Physical form

Lyophilized powder stabilized with lactose and dextran

Legal Information

Sepharose is a trademark of Cytiva


存储类别

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

法规信息

新产品

此项目有



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

没有发现合适的版本?

如果您需要特殊版本,可通过批号或批次号查找具体证书。

已有该产品?

在文件库中查找您最近购买产品的文档。

访问文档库



Michael T Forrester et al.
Journal of lipid research, 52(2), 393-398 (2010-11-04)
Protein S-acylation is a major posttranslational modification whereby a cysteine thiol is converted to a thioester. A prototype is S-palmitoylation (fatty acylation), in which a protein undergoes acylation with a hydrophobic 16 carbon lipid chain. Although this modification is a
Markandeswar Panda et al.
Journal of chromatography. A, 1202(1), 75-82 (2008-07-08)
Green fluorescent protein (GFP) fused to the C-terminal 100 amino acids of CAAT enhancer binding protein (C/EBP) also containing an N-terminal (His)(6) tag (GFP-C/EBP) was used as a transcription factor model to test whether thiol-disulfide exchange reactions could be used
F Desarnaud et al.
Journal of chromatography, 603(1-2), 95-104 (1992-06-19)
The major problem usually encountered in the application of the (strept)avidin-biotin system to the purification of proteins (or other biological molecules) lies in the difficult reversion of the interaction between immobilized (strept)avidin and the adsorbed biotinylated protein. Among the proposed