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安全信息

RAB1027

Sigma-Aldrich

人CD59 ELISA试剂盒

for cell culture supernatants, plasma, and serum samples

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About This Item

UNSPSC代码:
41116158
NACRES:
NA.32

种属反应性

human

包装

kit of 96 wells (12 strips x 8 wells)

技术

ELISA: suitable

输入

sample type cell culture supernatant(s)
sample type serum sample(s)
sample type plasma

assay range

inter-assay cv: <12%
intra-assay cv: <10%
sensitivity: 40 pg/ml

检测方法

colorimetric

运输

wet ice

储存温度

−20°C

基因信息

human ... CD59(966)

一般描述

This ELISA antibody pair detects human CD59. Other species are not determined.

应用

For research use only. Not for use in diagnostic procedures.
Please refer to the attached Protocolfor details.

其他说明

A sample Certificate of Analysis is available for this product. Please type the word sample in the text box provided for lot number.

象形图

Corrosion

警示用语:

Warning

危险声明

预防措施声明

危险分类

Met. Corr. 1

储存分类代码

8A - Combustible corrosive hazardous materials

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sheng-Wei Luo et al.
Fish & shellfish immunology, 89, 486-497 (2019-04-14)
CD59, a multifunctional glycoprotein, not only plays a regulatory role in complement cascades, but also participates in modulation of teleostean immunity. In this study, full length sequence of EcCD59 was obtained, comprising a 5'UTR of 163 bp, an ORF of
Yang Yie Sio et al.
Scientific reports, 10(1), 715-715 (2020-01-22)
Post-glycosylphosphatidylinositol (GPI) attachment to proteins 3, also known as PGAP3 or PERLD1 (PER1-like domain-containing protein 1), participates in the lipid remodeling process of glycosylphosphatidylinositol (GPI) anchor proteins during post-translational modification. Functional defect in PERLD1 was previously hypothesized to influence this
Diego Martínez-López et al.
Journal of the American College of Cardiology, 75(16), 1926-1941 (2020-04-25)
The mechanisms underlying early atherosclerotic plaque formation are not completely understood. Moreover, plasma biomarkers of subclinical atherosclerosis are lacking. The purpose of this study was to analyze the temporal and topologically resolved protein changes taking place in human aortas with

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