Catalog No.
PHB89401
Species reactivity
Human, Mouse, Rat
Host species
Rabbit
Isotype
IgG
Clonality
Polyclonal
Immunogen
E. coli - derived recombinant Human SERPINC1 (His33-Lys464).
Tested applications
ELISA: 1:4000-1:8000, IHC: 1:50-1:100, WB: 1:1000-1:4000
Target
Serpin C1, ATIII, AT3, SERPINC1, Antithrombin-III
Purification
Purified by antigen affinity column.
Accession
P01008
Applications
ELISA, IHC, WB
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Corrigendum: Synergistic effects of nab-PTX and anti-PD-1 antibody combination against lung cancer by regulating Pi3K/AKT pathway through the Serpinc1 gene., PMID:38023118
Kawasaki Disease and Coronary Artery Involvement: A Narrative Review., PMID:36185934
Synergistic effects of nab-PTX and anti-PD-1 antibody combination against lung cancer by regulating the Pi3K/AKT pathway through the Serpinc1 gene., PMID:35992834
Liver gene regulation of hemostasis-related factors is altered by experimental snake envenomation in mice., PMID:32479494
Mouse venous thrombosis upon silencing of anticoagulants depends on tissue factor and platelets, not FXII or neutrophils., PMID:30898865
Thrombophilia Associated with Early Post-angioplasty Thrombosis of Dialysis Vascular Access., PMID:30066093
Emerging Therapeutic Strategies in the Treatment of Hemophilia A., PMID:28750425
Alcohol Consumption, High-Density Lipoprotein Cholesterol, Antithrombin III, and Body Mass Index Are Associated with Great Saphenous Vein Reflux in the Thigh., PMID:28501660
Hypoglycosylation is a common finding in antithrombin deficiency in the absence of a SERPINC1 gene defect., PMID:27214821
Role of platelets, neutrophils, and factor XII in spontaneous venous thrombosis in mice., PMID:26932804
Screening for potential serum biomarkers in rat mesangial proliferative nephritis., PMID:26791873
Identification and function probing of an antithrombin IIIβ conformation-specific antibody., PMID:26581031
Molecular basis and thrombotic manifestations of antithrombin deficiency in 15 unrelated Chinese patients., PMID:23932013
Prevalence of hereditary antithrombin mutations is higher than estimated in patients with thrombotic events., PMID:23429250
For research use only. Not for human or drug use.
