tPA rabbit pAb

tPA rabbit pAb

AO-06-ES6601-50

tPA rabbit pAb 50μL

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Antibody Product Overview

ELK.NoES6601
Product nametPA rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other namePLAT; Tissue-type plasminogen activator; t-PA; t-plasminogen activator; tPA; Alteplase; Reteplase
Size50μL
Unit price ($)148
Human gene ID5327
Human Swiss-ProtP00750
SourceRabbit
IsotypeIgG
TargettPA
Fields>>Apelin signaling pathway;>>Complement and coagulation cascades;>>Transcriptional misregulation in cancer;>>Prostate cancer;>>Fluid shear stress and atherosclerosis
Gene namePLAT
Protein nameTissue-type plasminogen activator
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID18791
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP11214
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID25692
Rat gene linkView Rat Gene
Rat Swiss-ProtP19637
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human tPA. AA range:38-87
SpecificitytPA Polyclonal Antibody detects endogenous levels of tPA protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/10000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)63kD
BackgroundThis gene encodes tissue-type plasminogen activator, a secreted serine protease that converts the proenzyme plasminogen to plasmin, a fibrinolytic enzyme. The encoded preproprotein is proteolytically processed by plasmin or trypsin to generate heavy and light chains. These chains associate via disulfide linkages to form the heterodimeric enzyme. This enzyme plays a role in cell migration and tissue remodeling. Increased enzymatic activity causes hyperfibrinolysis, which manifests as excessive bleeding, while decreased activity leads to hypofibrinolysis, which can result in thrombosis or embolism. Alternative splicing of this gene results in multiple transcript variants, at least one of which encodes an isoform that is proteolytically processed. [provided by RefSeq, Jan 2016],
Functioncatalytic activity:Specific cleavage of Arg-|-Val bond in plasminogen to form plasmin.,disease:Increased activity of TPA is the cause of hyperfibrinolysis [MIM:173370]. Hyperfibrinolysis leads to excessive bleeding. Defective release of TPA causes hypofibrinolysis, leading to thrombosis or embolism.,domain:Both FN1 and EGF-like domains are important for binding to LRP1.,domain:Both FN1 and one of the kringle domains are required for binding to fibrin.,domain:The FN1 domain mediates binding to annexin A2.,domain:The second kringle domain is implicated in binding to cytokeratin-8 and to the endothelial cell surface binding site.,function:Converts the abundant, but inactive, zymogen plasminogen to plasmin by hydrolyzing a single Arg-Val bond in plasminogen. By controlling plasmin-mediated proteolysis, it plays an important role in tissue remodeling and degradation, in cell migration and man
Subcellular locationSecreted, extracellular space.
ExpressionSynthesized in numerous tissues (including tumors) and secreted into most extracellular body fluids, such as plasma, uterine fluid, saliva, gingival crevicular fluid, tears, seminal fluid, and milk.

Additional Images

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Western Blot analysis of A549 cells using tPA Polyclonal Antibody. Secondary antibody(catalog#:RS0002) was diluted at 1:20000
Image 2
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Western blot analysis of lysate from A549 cells, using tPA antibody.
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: AO-06-ES6601-50
: 10 Produits
Hurry! only 10 items left in stock.

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