RAB0556
人VWF / von Willebrand因子ELISA试剂盒
for serum, plasma, cell culture supernatants and urine
别名:
VWF ELISA试剂盒
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关于此项目
NACRES:
NA.32
UNSPSC Code:
41116158
Gene information:
human ... VWF(7450)
Input:
sample type serum
sample type plasma
sample type cell culture supernatant(s)
sample type urine
sample type plasma
sample type cell culture supernatant(s)
sample type urine
Species reactivity:
human
Storage temp.:
−20°C
Shipped in:
wet ice
species reactivity
human
packaging
kit of 96 wells (12 strips x 8 wells)
technique(s)
ELISA: suitable
input
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
detection method
colorimetric
shipped in
wet ice
storage temp.
−20°C
Gene Information
human ... VWF(7450)
General description
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。
Application
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）
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）
Other Notes
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 。
请在批号对应的文本框中输入单词 sample 。
signalword
Warning
hcodes
pcodes
Hazard Classifications
Met. Corr. 1
flash_point_f
Not applicable
flash_point_c
Not applicable
存储类别
10 - Combustible liquids
法规信息
常规特殊物品
低风险生物材料
此项目有
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| RAB0556-1KT | 04061834963561 |