PIPA143058
CD142 Polyclonal Antibody, Invitrogen™
Manufacturer: Thermo Scientific
Select a Size
| Pack Size | SKU | Availability | Price |
|---|---|---|---|
| Each of 1 | PIPA143058-Each-of-1 | In Stock | ₹ 29,147.50 |
PIPA143058 - Each of 1
In Stock
Quantity
1
Base Price: ₹ 29,147.50
GST (18%): ₹ 5,246.55
Total Price: ₹ 34,394.05
Antigen
CD142
Classification
Polyclonal
Conjugate
Unconjugated
Gene
F3
Gene Alias
AA409063; CD142; Cf3; Cf-3; Coagulation factor III; coagulation factor III (thromboplastin, tissue factor); coagulation factor III, tissue factor; F3; TF; TFA; Thromboplastin; Tissue factor
Host Species
Sheep
Purification Method
Ammonium sulfate precipitation, Ion-exchange chromatography
Regulatory Status
RUO
Gene ID (Entrez)
2152
Content And Storage
-20° C, Avoid Freeze/Thaw Cycles
Form
Liquid
Applications
ELISA, Western Blot
Concentration
13.0 mg/mL
Formulation
50% water with 50% glycerol and no preservative
Gene Accession No.
P13726
Gene Symbols
F3
Immunogen
Human Tissue Factor.
Quantity
1 mg
Primary or Secondary
Primary
Target Species
Human
Product Type
Antibody
Isotype
IgG
Related Products
Description
- PA1-43058 detects Tissue Factor in human samples
- PA1-43058 has successfully been used in Western blot and ELISA applications
- PA1-43058 was derived from human tissue factor
- 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.