VWF (Human) ELISA Kit
产品名称: VWF (Human) ELISA Kit
英文名称: VWF (Human) ELISA Kit
产品编号: KA0512
产品价格: 0
产品产地: 台湾
品牌商标: Abnova
更新时间: null
使用范围: null
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- Specification
- Product Description:
- VWF (Human) ELISA Kit is a sandwich enzyme immunoassay for the quantitative measurement of human VWF.
- Calibration Range:
- 2.5 to 80 mU/mL
- Limit of Detection:
- 2.5 mU/mL
- Reactivity:
- Human
- Storage Instruction:
- Store SP Conjugate and Biotinylated Antibody and Standard at -20°C.
Store all other components at 4°C.
- Quality Control Testing:
- Standard curve
The standard curve is for the purpose of illustration only and should not be used to calculate unknowns. A standard curve should be generated each time the assay is performed.
- Protocol:
- Protocol Download
- MSDS:
- Download
- Suitable Sample:
- Cell Culture Supernatant, Plasma, Serum
- Sample Volume:
- 50 uL
- Label:
- Biotin-conjugate
- Detection Method:
- Colorimetric
- Intra-Assay:
- 5.1%
- Inter-Assay:
- 7.2%
- Spiking Recovery:
- 100.5%
- Regulation Status:
- For research use only (RUO)
- Publication Reference
- 1.
- Evaluation of a new automated ELISA test for von Willebrand factor using two monoclonal antibodies.
Pittet JL, Barbalat V, Sanvert M, Villard C, Jorieux S, Mazurier C.Blood Coagul Fibrinolysis. 1997 Jun;8(4):209-15.
- 2.
- Soluble circulating cell adhesion molecules in haemolytic uraemic syndrome.
Inward CD, Pall AA, Adu D, Milford DV, Taylor CM.Pediatr Nephrol. 1995 Oct;9(5):574-8.
- 3.
- The interaction between collagens and factor VIII/von Willebrand factor: investigation of the structural requirements for interaction.
Morton LF, Griffin B, Pepper DS, Barnes MJ.Thromb Res. 1983 Dec 15;32(6):545-56.
- Application Image
- Quantification
- Entrez GeneID:
- 7450
- Gene Name:
- VWF
- Gene Alias:
- F8VWF,VWD
- Gene Description:
- von Willebrand factor
- Omim ID:
- 193400
- Gene Ontology:
- Hyperlink
- Gene Summary:
- The glycoprotein encoded by this gene functions as both an antihemophilic factor carrier and a platelet-vessel wall mediator in the blood coagulation system. It is crucial to the hemostasis process. Mutations in this gene or deficiencies in this protein result in von Willebrand's disease. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq
- Other Designations:
- coagulation factor VIII VWF
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