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Arterial Thrombosis: Disease Bioinformatics

Thrombosis is the interruption of blood flow by a clot in the blood vessels. Arterial Thrombosis is when a blood clot forms in the arteries, which are the blood vessels that carry oxygenated blood from the heart to the rest of the body. Arterial Thrombosis can be caused by obesity, particular medications, pregnancy, recent fracture or broken bone, prolonged immobility, obesity, and treatment for cancer. Symptoms of Arterial Thrombosis include varicose veins, swelling in the extremities, numbness, and isolated pain. Arterial Thrombosis can be treated with anti-clotting medications, enzymes that brake down the clot, and catheters to expand the affected vein. About 25% of Arterial Thrombosis cases require an amputation and there is a possibility that the thrombosis can recur.

Arterial Thrombosis Bioinformatics Tool

Laverne is a handy bioinformatics tool to help facilitate scientific exploration of related genes, diseases and pathways based on co-citations. Explore more on Arterial Thrombosis below! For more information on how to use Laverne, please read the How to Guide.
Vizit™, under license from BioVista Inc.

Top Research Reagents

We have 1265 products for the study of Arterial Thrombosis that can be applied to Flow Cytometry, Western Blot, Immunocytochemistry/Immunofluorescence, Immunohistochemistry from our catalog of antibodies and ELISA kits.

Other PRH2 Recombinant Protein

Species Human
Applications WB, ELISA, PA

Immunocytochemistry/Immunofluorescence: Von Willebrand Factor Antibody [NB600-586]Immunohistochemistry-Paraffin: Von Willebrand Factor Antibody [NB600-586] - Staining of formalin-fixed, paraffin-embedded Human Kidney sections with 1:2,000 Rabbit Anti-von Willebrand Factor.

Rabbit Polyclonal
Species Human
Applications ICC/IF, IHC, IHC-P

2 Publications
Immunohistochemistry: Factor V Antibody [NBP1-88114] - Staining of human cerebellum shows strong cytoplasmic positivity in purkinje cells.

Rabbit Polyclonal
Species Human
Applications IHC, IHC-P

Western Blot: Plasminogen Antibody [NB600-930] - Lane 1: Plasminogen. Lane 2: None. Load: 50 ng per lane. Primary antibody: Plasminogen primary antibody at 1:1,000 overnight at 4C. Secondary antibody: Peroxidase goat secondary antibody at 1:40,000 for 60 min at RT. Blocking: incubated with blocking buffer for 30 min at RT. Predicted/Observed size: 91 kDa, 91 kDa for Plasminogen. Other band(s): None.Western Blot: Plasminogen Antibody [NB600-930] - Detection of Plasminogen under reducing (R) and non-reducing (NR) conditions. Reduced samples of purified target proteins contained 4% BME and were boiled for 5 minutes. Samples of 1ug of protein per lane were run by SDS-PAGE. Protein was transferred to nitrocellulose and probed with 1:3000 dilution of primary antibody. Detection shown was using Dylight 649 conjugated Donkey anti goat 1 hr RT.

Goat Polyclonal
Species Human, Bacteria
Applications WB, ELISA

     2 Reviews

7 Publications
Western Blot: Coagulation Factor X Antibody [NBP1-33320] -  Sample (30 ug of whole cell lysate) A: Hela 10% SDS PAGE; antibody diluted at 1:1000.Immunocytochemistry/Immunofluorescence: Coagulation Factor X Antibody [NBP1-33320] -  Methanol-fixed HeLa, using Factor X antibody at 1:200 dilution.

Rabbit Polyclonal
Species Human, Mouse
Applications WB, ICC/IF, IHC

Western blot shows lysates of HUVEC human umbilical vein endothelial cells and HepG2 human hepatocellular carcinoma cell line. PVDF membrane was probed with 1:1000 dilution of Rabbit Anti-Human Serpin E1/PAI‑1 Monoclonal Antibody (Catalog # MAB17861) followed by HRP-conjugated Anti-Rabbit IgG Secondary Antibody (Catalog # <A class=NoLineLink href=Simple Western lane view shows lysates of HUVEC human umbilical vein endothelial cells, loaded at 0.2 mg/mL. A specific band was detected for Serpin E1/PAI‑1 at approximately 55 kDa (as indicated) using 1:100 dilution of Rabbit Anti-Human Serpin E1/PAI‑1 Monoclonal Antibody (Catalog # MAB17861). This experiment was conducted under reducing conditions and using the 12-230 kDa separation system.        Non-specific interaction with the 230 kDa Simple Western standard may be seen with this antibody.

Species Human
Applications WB, Simple Western

Western Blot: SH2B2 Antibody [NBP2-13305] - Lane 1: Marker [kDa] 250, 130, 95, 72, 55, 36, 28, 17, 10<br/>Lane 2: Human cell line RT-4<br/>Lane 3: Human cell line U-251MG spImmunocytochemistry/Immunofluorescence: SH2B2 Antibody [NBP2-13305] - Staining of human cell line MCF7 shows positivity in cytoplasm.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC

Western Blot: RNF130 Antibody [NBP1-81858] - Lane 1: Marker [kDa] 230, 130, 95, 72, 56, 36, 28, 17, 11<br/>Lane 2: Human cell line RT-4Immunocytochemistry/Immunofluorescence: RNF130 Antibody [NBP1-81858] - Staining of human cell line U-2 OS shows positivity in nucleus & cytoplasm.

Rabbit Polyclonal
Species Human
Applications WB, ICC/IF, IHC

Immunohistochemistry-Paraffin: Tenascin C Antibody (4C8MS) [NB110-68136] - Immunohistochemical analysis of Tenascin C on mouse bone and tendon using NB110-68136.Flow Cytometry: Tenascin C Antibody (4C8MS) [NB110-68136] - Intracellular flow cytometric staining of 1 x 10^6 MCF-7 cells using Tenascin C antibody (dark blue). Isotype control shown in orange. An antibody concentration of 1 ug/1x10^6 cells was used.

Mouse Monoclonal
Species Human, Mouse, Rat
Applications WB, ELISA, Flow

17 Publications
Western Blot: MTHFR Antibody (1G12) [H00004524-M03] - Western Blot detection against Immunogen (H00004524-P01) (34.14 KDa).Immunocytochemistry/Immunofluorescence: MTHFR Antibody (1G12) [H00004524-M03] - Analysis of monoclonal antibody to MTHFR on HeLa cell. Antibody concentration 10 ug/ml

Mouse Monoclonal
Species Human
Applications WB, ELISA, ICC/IF

3 Publications