Mouse F5 ELISA Kit (V2LY-0626-LY2185)

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Tested Data
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Datasheet Target References Q & As Review & reward Protocols Associated Products

Basic Information

Sensitivity
9.61 ng/mL
Detection Range
20-4500 ng/mL
Sample Type
Serum, Plasma, cell culture supernates
Specificity
Mouse
Assay Type
Sandwich
Reactivity
Mouse
Assay Time
1.5 h
Molecule Mass
247.2 kDa
Components
  • Pre-coated ELISA plate: 12 wells * 8 detachable strips
  • Standard solution: 0.5ml x1
  • Standard diluent: 3ml x1
  • Streptavidin-HRP: 6ml x1
  • Stop solution: 6ml x1
  • Substrate solution A: 6ml x1
  • Substrate solution B: 6ml x1
  • Wash buffer concentrate (25x): 20ml x1
  • Biotinylated antibody: 1ml x1

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 2-8°C
More Infomation

Target

Full Name
Coagulation Factor V
Research Area
Central regulator of hemostasis. It serves as a critical cofactor for the prothrombinase activity of factor Xa that results in the activation of prothrombin to thrombin.
Biological Process
Blood circulation Source: GO_Central
Blood coagulation Source: GO_Central
Cellular Location
Secreted
Involvement in disease
Factor V deficiency (FA5D):
A blood coagulation disorder leading to a hemorrhagic diathesis known as parahemophilia.
Thrombophilia due to activated protein C resistance (THPH2):
A hemostatic disorder due to defective degradation of factor V by activated protein C. It is characterized by a poor anticoagulant response to activated protein C resulting in tendency to thrombosis.
Budd-Chiari syndrome (BDCHS):
A syndrome caused by obstruction of hepatic venous outflow involving either the hepatic veins or the terminal segment of the inferior vena cava. Obstructions are generally caused by thrombosis and lead to hepatic congestion and ischemic necrosis. Clinical manifestations observed in the majority of patients include hepatomegaly, right upper quadrant pain and abdominal ascites. Budd-Chiari syndrome is associated with a combination of disease states including primary myeloproliferative syndromes and thrombophilia due to factor V Leiden, protein C deficiency and antithrombin III deficiency. Budd-Chiari syndrome is a rare but typical complication in patients with polycythemia vera.
Ischemic stroke (ISCHSTR):
A stroke is an acute neurologic event leading to death of neural tissue of the brain and resulting in loss of motor, sensory and/or cognitive function. Ischemic strokes, resulting from vascular occlusion, is considered to be a highly complex disease consisting of a group of heterogeneous disorders with multiple genetic and environmental risk factors.
Pregnancy loss, recurrent, 1 (RPRGL1):
A common complication of pregnancy, resulting in spontaneous abortion before the fetus has reached viability. The term includes all miscarriages from the time of conception until 24 weeks of gestation. Recurrent pregnancy loss is defined as 3 or more consecutive spontaneous abortions.
PTM
Thrombin activates factor V proteolytically to the active cofactor, factor Va (formation of a heavy chain at the N-terminus and a light chain at the C-terminus).
Sulfation is required for efficient thrombin cleavage and activation and for full procoagulant activity.
Activated protein C inactivates factor V and factor Va by proteolytic degradation.
Phosphorylated by FAM20C in the extracellular medium.

Andresen, M. S., Sletten, M., Sandset, P. M., Iversen, N., Stavik, B., & Tinholt, M. (2022). Coagulation Factor V (F5) is an Estrogen-Responsive Gene in Breast Cancer Cells. Thrombosis and Haemostasis, 122(08), 1288-1295.

Castoldi, E. (2021). F5‐Atlanta: Factor V‐short strikes again. Journal of Thrombosis and Haemostasis, 19(7), 1638.

Su, K., Wang, L., Wang, M., & Wang, H. (2021). A novel mutation (Ser951LeufsTer8) in F5 gene leads to hereditary coagulation factor V deficiency. Blood Coagulation & Fibrinolysis, 32(2), 140-145.

Lind, S. M. (2021). The role of coagulation factor V in breast cancer: effect on treatment response (Master's thesis, Norwegian University of Life Sciences, Ås).

Tinholt, M., Stavik, B., Tekpli, X., Garred, Ø., Borgen, E., Kristensen, V., ... & Iversen, N. (2020). Coagulation factor V is a marker of tumor-infiltrating immune cells in breast cancer. Oncoimmunology, 9(1), 1824644.

Liu, M., Yang, Y., & Liu, Y. (2020). Identification of a novel variant of F5 gene in a consanguineous pedigree affected with inherited coagulation factor V deficiency. Zhonghua yi xue yi Chuan xue za zhi= Zhonghua Yixue Yichuanxue Zazhi= Chinese Journal of Medical Genetics, 37(5), 505-508.

Tabibian, S., Shiravand, Y., Shams, M., Safa, M., Gholami, M. S., Heydari, F., ... & Dorgalaleh, A. (2019, July). A comprehensive overview of coagulation factor V and congenital factor V deficiency. In Seminars in thrombosis and hemostasis (Vol. 45, No. 05, pp. 523-543). Thieme Medical Publishers.

Paraboschi, E. M., Menegatti, M., Peyvandi, F., Duga, S., & Asselta, R. (2019). Understanding the impact of aberrant splicing in coagulation factor V deficiency. International Journal of Molecular Sciences, 20(4), 910.

Tinholt, M., Garred, Ø., Borgen, E., Beraki, E., Sletten, M., Sahlberg, K. K., ... & Iversen, N. (2018). Coagulation factor V is expressed in tumors and predicts favorable outcome in aggressive breast cancer. Thrombosis Research, 164, S183.

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For research use only. Not intended for any clinical use.

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