F7 (Human) ELISA Kit
产品名称： F7 (Human) ELISA Kit
英文名称： F7 (Human) ELISA Kit
产品编号： KA0471
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
亚诺法生技股份有限公司（Abnova)
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- Specification
- Product Description:
- F7 (Human) ELISA Kit is a sandwich enzyme immunoassay for the quantitative measurement of human F7.
- Calibration Range:
- 6.25 to 200 ng/mL
- Limit of Detection:
- 6 ng/mL
- Reactivity:
- Human
- Storage Instruction:
- Store the kit 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, Saliva, Serum
- Sample Volume:
- 50 uL
- Label:
- Biotin-conjugate
- Detection Method:
- Colorimetric
- Intra-Assay:
- 4.9%
- Inter-Assay:
- 7.1%
- Spiking Recovery:
- 97%
- Regulation Status:
- For research use only (RUO)
- Publication Reference
- 1.
- Coagulation factor VII and the risk of coronary heart disease in healthy men.
Junker R, Heinrich J, Schulte H, van de Loo J, Assmann G.Arterioscler Thromb Vasc Biol. 1997 Aug;17(8):1539-44.
- 2.
- Severe factor VII deficiency due to a mutation disrupting a hepatocyte nuclear factor 4 binding site in the factor VII promoter.
Arbini AA, Pollak ES, Bayleran JK, High KA, Bauer KA.Blood. 1997 Jan 1;89(1):176-82.
- 3.
- Isolation and characterization of bovine factor VII.
Kisiel W, Davie EW.Biochemistry. 1975 Nov 4;14(22):4928-34.
- Application Image
- Quantification
- Entrez GeneID:
- 2155
- Gene Name:
- F7
- Gene Alias:
- -
- Gene Description:
- coagulation factor VII (serum prothrombin conversion accelerator)
- Omim ID:
- 227500
- Gene Ontology:
- Hyperlink
- Gene Summary:
- This gene encodes coagulation factor VII which is a vitamin K-dependent factor essential for hemostasis. This factor circulates in the blood in a zymogen form, and is converted to an active form by either factor IXa, factor Xa, factor XIIa, or thrombin by minor proteolysis. Upon activation of the factor VII, a heavy chain containing a catalytic domain and a light chain containing 2 EGF-like domains are generated, and two chains are held together by a disulfide bond. In the presence of factor III and calcium ions, the activated factor then further activates the coagulation cascade by converting factor IX to factor IXa and/or factor X to factor Xa. Alternative splicing of this gene results in 2 transcripts. Defects in this gene can cause coagulopathy. [provided by RefSeq
- Other Designations:
- FVII coagulation protein,OTTHUMP00000018733,OTTHUMP00000018734,coagulation factor VII,eptacog alfa
- Interactome
- Gene Pathway
- Related Disease
- Abortion, Habitual
- Activated Protein C Resistance
- Acute Disease
- Alzheimer Disease
- Alzheimer disease
- Amyotrophic Lateral Sclerosis
- Amyotrophic lateral sclerosis
- Anemia, Sickle Cell
- Anemia, sickle cell
- Angina Pectoris
- Angina, Unstable
- Arterial Occlusive Diseases
- Arteriosclerosis
- Atherosclerosis
- Atherosclerosis
- Atrial Fibrillation
- Birth Weight
- Blood Coagulation Disorders
- Body Weight