推荐产品
生物来源
heparin from Porcine intestinal mucosa
质量水平
类型
Type I
表单
saline suspension
标记范围
400-1500 μg per mL packed gel (activity approx. 140 USP units per mg)
技术
affinity chromatography: suitable
基质
cross-linked 4% beaded agarose
基质活化
cyanogen bromide
基质附着
amino
基质隔离区
1 atom
适用性
suitable for chromatography
储存温度
2-8°C
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应用
Heparin-agarose is developed from porcine intestinal mucosa and is used in affinity chromatography. Heparin-agarose has been used in studies to provide information on human monocytic ehrlichiosis, tumor necrosis and the effects of coagulation from Vipera snake venom.
外形
Suspension in 0.5 M NaCl containing preservative
储存分类代码
10 - Combustible liquids
WGK
WGK 3
闪点(°F)
Not applicable
闪点(°C)
Not applicable
个人防护装备
Eyeshields, Gloves, type N95 (US)
历史批次信息供参考:
分析证书(COA)
Lot/Batch Number
Alejandra Loyola et al.
Methods (San Diego, Calif.), 31(1), 96-103 (2003-08-02)
It is becoming clear that the structure of cellular chromatin is dynamic and capable of undergoing rapid changes to respond to the metabolic requirements of the cell. These changes have a direct impact on gene expression and, therefore, the chromatin
L C Andersen et al.
The Journal of experimental medicine, 173(1), 181-192 (1991-01-01)
Class II genes of the human major histocompatibility complex (MHC) are highly polymorphic. Allelic variation of structural genes provides diversity in immune cell interactions, contributing to the formation of the T cell repertoire and to susceptibility to certain autoimmune diseases.
G Glaser et al.
Archives of virology, 143(10), 1967-1983 (1998-12-18)
The immediate early BRLF1 and BZLF1 promoters of Epstein-Barr virus are crucial for triggering the replicative cycle of the virus. To better understand the cell type dependence of the lytic cycle we conducted an analysis of the BRLF1-promoter in the
91. Universal purification of AAV serotypes 1?5 modified to contain a heparin binding epitope.
Faust, S.M., et al.
Molecular Therapy, 9, S36-S36 (2004)
Analysis of Adeno-Associated Virus and HPV Interaction.
Hermonat, P.L., et al.
Methods in Molecular Medicine, 119, 397-409 (2006)
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