catalog number :
MBS702904
products type :
ELISA Kit
products full name :
Human tissue factor, TF ELISA Kit
products short name :
coagulation factor III (thromboplastin, tissue factor)
products name syn :
Human tissue factor (TF) ELISA kit; CD142; TF; TFA; coagulation factor III; tissue factor; coagulation factor III (thromboplastin; tissue factor)
other names :
tissue factor isoform 2; Tissue factor; tissue factor; coagulation factor III (thromboplastin, tissue factor); Coagulation factor III; Thromboplastin; CD_antigen: CD142
other gene names :
F3; F3; TF; TFA; CD142; TF
uniprot entry name :
TF_HUMAN
specificity :
This assay has high sensitivity and excellent specificity for detection of Human TF. No significant cross-reactivity or interference between Human TF and analogues was observed.
storage stability :
Unopened test kits should be stored at 2 to 8 degree C upon receipt. Please refer to pdf manual for further storage instructions.
other info1 :
Intra-assay Precision: Intra-assay Precision (Precision within an assay): CV% is less than 8%. Three samples of known concentration were tested twenty times on one plate to assess. Inter-assay Precision (Precision between assays): CV% is less than 10%. Three samples of known concentration were tested in twenty assays to assess. Sample Type: serum, plasma, tissue homogenates. Detection Range: 3.12 pg/ml -200 pg/ml. Detection Wavelength: 450 nm. Sensitivity: 0.78 pg/ml
other info2 :
Sample Volume: 50-100ul. Protein Biological Process 1: Blood Coagulation. Protein Biological Process 3: Blood coagulation
products description :
Principle of the Assay: The microtiter plate provided in this kit has been pre-coated with an antibody specific to TF. Standards or samples are then added to the appropriate microtiter plate wells with a biotin-conjugated antibody preparation specific for TF and Avidin conjugated to Horseradish Peroxidase (HRP) is added to each microplate well and incubated. Then a TMB (3,3',5,5' tetramethyl-benzidine) substrate solution is added to each well. Only those wells that contain TF, biotin-conjugated antibody and enzyme-conjugated Avidin will exhibit a change in color. The enzyme-substrate reaction is terminated by the addition of a sulphuric acid solution and the color change is measured spectrophotometrically at a wavelength of 450 nm +/- 2 nm. The concentration of TF in the samples is then determined by comparing the O.D. of the samples to the standard curve.
ncbi acc num :
NP_001171567.1
ncbi gb acc num :
NM_001178096.1
ncbi mol weight :
33,068 Da
ncbi pathways :
Complement And Coagulation Cascades Pathway 198880!!Complement And Coagulation Cascades Pathway 83073!!Complement And Coagulation Cascades Pathway 484!!Extrinsic Pathway 106058!!Formation Of Fibrin Clot (Clotting Cascade) Pathway 106057!!Hemostasis Pathway 106028
ncbi summary :
This gene encodes coagulation factor III which is a cell surface glycoprotein. This factor enables cells to initiate the blood coagulation cascades, and it functions as the high-affinity receptor for the coagulation factor VII. The resulting complex provides a catalytic event that is responsible for initiation of the coagulation protease cascades by specific limited proteolysis. Unlike the other cofactors of these protease cascades, which circulate as nonfunctional precursors, this factor is a potent initiator that is fully functional when expressed on cell surfaces. There are 3 distinct domains of this factor: extracellular, transmembrane, and cytoplasmic. This protein is the only one in the coagulation pathway for which a congenital deficiency has not been described. Alternate splicing results in multiple transcript variants.[provided by RefSeq, May 2010]
uniprot summary :
Function: Initiates blood coagulation by forming a complex with circulating factor VII or VIIa. The [TF:VIIa] complex activates factors IX or X by specific limited protolysis. TF plays a role in normal hemostasis by initiating the cell-surface assembly and propagation of the coagulation protease cascade.1 PublicationManual assertion based on experiment in:Ref.6