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- 文献和实验
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- 库存:
大量
- 供应商:
AssayPro
- 检测范围:
0.007 μg/ml
- 检测方法:
ELISA
- 应用:
血浆、细胞培养上清液
- 样本:
100 μl
- 规格:
96 wells
因子FVIIa发色底物法活性试剂盒
Introduction
Factor VII (FVII) is a vitamin K-dependent plasma glycoprotein that is synthesized in the liver and circulates in blood as a single-chain inactive zymogen with a molecular mass of 50 kDa (1). Upon tissue damage and vascular injury, the cell surface receptor and cofactor tissue factor (TF) binds and allosterically activates FVII to its active form, FVIIa. The TF/FVIIa complex catalyzes the conversion of both factor IX to factor IXa and factor X to factor Xa to initiate coagulation via the extrinsic pathway (2, 3). Very low levels of FVII are associated with severe coagulation disorders (4). Elevated plasma levels of FVII coagulant activity constitute an independent risk factor for fatal outcomes of coronary heart disease in middle-aged men (5).
Principle of Assay
The AssaySense Human FVIIa Chromogenic Activity Assay Kit is developed to determine human FVIIa activity in plasma and cell culture supernatants. The assay couples immunofunctional and indirect amidolytic assay. A polyclonal antibody specific for human FVIIa has been pre-coated onto a microplate and FVIIa is bound to the immobilized antibody. The assay measures the ability of FVIIa to activate factor X (FX) to factor Xa. The amidolytic activity of the FVIIa is quantitated by the amount of FXa produced using a highly specific FXa substrate releasing a yellow para-nitroaniline (pNA) chromophore. The change in absorbance of the pNA at 405 nm is directly proportional to the FVIIa enzymatic activity.
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文献和实验【申请上传】Current Protocols in Immunology
and Human Interleukin 9 Unit 6.14 Measurement of Mouse and Human Interleukin 10 Unit 6.15 Measurement of Human Interleukin 11 Unit 6.16 Measurement of Human and Mouse Interleukin-12 Unit 6.17 Measurement of Human and Murine Stem Cell Factor (c-kit Ligand
in liver as measured by bDNA assay and normalization to GAPDH mRNA was also demonstrated with normalization to three other liver mRNAs, including factor VII, glucose-6-phosphatase and VEGF (Supplementary Fig. 1). Determination of in vivo mechanism
that have abolished RNase H activity in real-time RT-PCR experiments. Unlike many other qRT-PCR kits, MessageSensor includes a total RNA control, a control human GAPDH primer set, RNase inhibitor, and nucleotides, as well as a buffer additive that enables detection
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