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Merck
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主要文件

RAB0556

Sigma-Aldrich

人VWF / von Willebrand因子ELISA试剂盒

for serum, plasma, cell culture supernatants and urine

别名:

VWF ELISA Kit

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About This Item

分類程式碼代碼:
41116158
NACRES:
NA.32

物種活性

human

包裝

kit of 96 wells (12 strips x 8 wells)

技術

ELISA: suitable

輸入

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

assay range

inter-assay cv: <10%
intra-assay cv: <12%
sensitivity: 0.4 ng/mL

檢測方法

colorimetric

運輸包裝

wet ice

儲存溫度

−20°C

基因資訊

human ... VWF(7450)

相关类别

一般說明

人VWF（血管性血友病因子）ELISA（酶联免疫吸附测定）试剂盒是一种体外检测，用于定量测定如血清、血浆、细胞培养物上清液、尿液或细胞和组织裂解液中的目标蛋白。

應用

人VWF（血管性血友病因子）ELISA试剂盒已被用于定量测定骨髓间充质干细胞（BMSL）和人脐静脉内皮细胞（HUVEC）中的内皮细胞标记物血管性血友病因子。
仅供研究使用。不可用于诊断操作。
请参考附带的一般ELISA试剂盒操作程序（三明治、竞争性 & 间接ELISA）

其他說明

本产品提供样本分析证书。
请在批号对应的文本框中输入单词 sample 。

试剂盒组分也可单独购买

产品编号
说明
化学品安全说明书
  • RABTMB3ELISA Colorimetric TMB Reagent (HRP Substrate, Item H)化学品安全说明书
  • RABSTOP3ELISA Stop Solution (Item I)化学品安全说明书
  • RABELADAELISA 1X Assay/Sample Diluent Buffer A (Item D1)化学品安全说明书
  • RABELADBELISA 5X Assay/Sample Diluent Buffer B (Item E1)化学品安全说明书
  • RABWASH420X Wash Buffer (Item B)化学品安全说明书

象形圖

Corrosion
GHS05

訊號詞

Warning

危險聲明

H290

防範說明

P234 - P390

危險分類

Met. Corr. 1

儲存類別代碼

8A - Combustible corrosive hazardous materials

閃點（°F）

Not applicable

閃點（°C）

Not applicable

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
0426K0006
1219J0006
1129J0006
1128J0006
0511I0006

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如果您需要特殊版本，可通过批号或批次号查找具体证书。

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J W R Sins et al.
Journal of thrombosis and haemostasis : JTH, 15(7), 1392-1402 (2017-05-01)
Essentials The role of von Willebrand Factor (VWF) in the pathophysiology of sickle cell disease is unclear. We assessed markers of VWF during admission for vaso-occlusive crisis (VOC) and steady state. VWF reactivity was higher during VOC and was associated
Claus Rieker et al.
Arteriosclerosis, thrombosis, and vascular biology, 39(9), e195-e207 (2019-07-19)
The ApoE (apolipoprotein) allele epsilon 4 is a major genetic risk factor for Alzheimer disease, cardiovascular disorders, and stroke, indicating that it significantly impacts cerebral and vascular systems. However, very little is known about how APOE genotype affects brain endothelial
Erika Kajdácsi et al.
The Journal of allergy and clinical immunology, 133(6), 1686-1691 (2014-02-14)
Hereditary angioedema (HAE) caused by C1-inhibitor (C1-INH) deficiency (HAE-C1-INH) is a potentially life-threatening rare disease caused by the decreased activity of C1-INH. Lack of C1-INH leads to overproduction of bradykinin, a potent vasoactive peptide. Although angioedema is induced by bradykinin
Camila M de Andrade et al.
International journal of biological macromolecules, 134, 653-659 (2019-05-10)
Endothelium plays an important modulatory role due to the synthesis and secretion of molecules that act on hemostasis and fibrinolysis. As there are no literature data about the effect of crotoxin (CTX) - the main component of Crotalus durissus terrificus
Junchao Duan et al.
Nanotoxicology, 12(5), 470-484 (2018-04-17)
Nowadays, nanotechnology environmental health and safety (nanoEHS) is gaining attention. We previously found that silica nanoparticles (SiNPs) could induce vascular endothelial damage. However, the subsequent toxicologic response to SiNPs-induced endothelial damage was still largely unknown. In this study, we explored
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