Rat Recombinant F2 protein, His Tag (V2LY-0526-LY9303)

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Basic Information

Expressed Host
HEK293 Cells
Protein Species
Rat
Tag
His Tag
Protein Construction
This product is Rat Recombinant F2 protein, His Tag consist of Amino Acid: 1-617 and predicts a molecular mass of 69.5 kDa.
Molecule Mass
69.5 kDa
Sequence
Amino Acid: 1-617
Species
Rat

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

Purity
>90% as determined by SDS-PAGE.
Endotoxin
Please contact us for more information.
Format
Lyophilized
Reconstitution
Allow the vial and reconstitution buffer to equilibrate to room temperature. Briefly centrifuge or tap down the vial to ensure that all lyophilized powder is collected at the bottom of the vial. For the reconstitution of this product, we recommend adding PBS or sterile water to achieve a final antibody concentration of 1 mg/mL. Allow the vial to reconstitute for 10-15 minutes at room temperature with gentle agitation. Avoid vigorous shaking that can cause foaming and antibody denaturation. Aliquot into volumes based on your experiment and store liquid protein at -20°C or -80°C for long time.
Buffer
Lyophilized from sterile PBS
Preservative
None
Storage
Samples are stable for up to twelve months from date of receipt at -20°C to -80°C. Store it under sterile conditions at -20°C to -80°C. It is recommended that the protein be aliquoted for optimal storage. Avoid repeated freeze-thaw cycles.
More Infomation

Target

Full Name
Coagulation Factor II, Thrombin
Research Area
Thrombin, which cleaves bonds after Arg and Lys, converts fibrinogen to fibrin and activates factors V, VII, VIII, XIII, and, in complex with thrombomodulin, protein C. Functions in blood homeostasis, inflammation and wound healing.
Biological Process
Acute-phase response Source: UniProtKB-KW
Antimicrobial humoral immune response mediated by antimicrobial peptide Source: UniProtKB
Blood coagulation Source: ProtInc
Cell surface receptor signaling pathway Source: BHF-UCL
Cytolysis by host of symbiont cells Source: UniProtKB
Fibrinolysis Source: UniProtKB
Multicellular organism development Source: ProtInc
Negative regulation of astrocyte differentiation Source: BHF-UCL
Negative regulation of cytokine production involved in inflammatory response Source: UniProtKB
Negative regulation of fibrinolysis Source: BHF-UCL
Negative regulation of platelet activation Source: BHF-UCL
Negative regulation of proteolysis Source: BHF-UCL
Neutrophil-mediated killing of gram-negative bacterium Source: UniProtKB
Platelet activation Source: BHF-UCL
Positive regulation of blood coagulation Source: BHF-UCL
Positive regulation of cell growth Source: Ensembl
Positive regulation of cell population proliferation Source: Ensembl
Positive regulation of collagen biosynthetic process Source: BHF-UCL
Positive regulation of lipid kinase activity Source: BHF-UCL
Positive regulation of phosphatidylinositol 3-kinase signaling Source: Ensembl
Positive regulation of phospholipase C-activating G protein-coupled receptor signaling pathway Source: BHF-UCL
Positive regulation of protein localization to nucleus Source: BHF-UCL
Positive regulation of protein phosphorylation Source: BHF-UCL
Positive regulation of reactive oxygen species metabolic process Source: UniProtKB
Positive regulation of receptor signaling pathway via JAK-STAT Source: BHF-UCL
Positive regulation of release of sequestered calcium ion into cytosol Source: BHF-UCL
Proteolysis Source: ProtInc
Regulation of blood coagulation Source: UniProtKB
Regulation of cell shape Source: Ensembl
Regulation of cytosolic calcium ion concentration Source: BHF-UCL
Response to wounding Source: BHF-UCL
Cellular Location
Extracellular space
Involvement in disease
Factor II deficiency (FA2D):
A very rare blood coagulation disorder characterized by mucocutaneous bleeding symptoms. The severity of the bleeding manifestations correlates with blood factor II levels.
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.
Thrombophilia due to thrombin defect (THPH1):
The disease is caused by variants affecting the gene represented in this entry. A common genetic variation in the 3-prime untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increased risk of venous thrombosis. A multifactorial disorder of hemostasis characterized by abnormal platelet aggregation in response to various agents and recurrent thrombi formation.
Pregnancy loss, recurrent, 2 (RPRGL2):
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
The gamma-carboxyglutamyl residues, which bind calcium ions, result from the carboxylation of glutamyl residues by a microsomal enzyme, the vitamin K-dependent carboxylase. The modified residues are necessary for the calcium-dependent interaction with a negatively charged phospholipid surface, which is essential for the conversion of prothrombin to thrombin.
N-glycosylated. N-glycan heterogeneity at Asn-121: Hex3HexNAc3 (minor), Hex4HexNAc3 (minor) and Hex5HexNAc4 (major). At Asn-143: Hex4HexNAc3 (minor) and Hex5HexNAc4 (major).
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For research use only. Not intended for any clinical use.

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