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Mouse Anti-PLG Recombinant Antibody (10A1) (CBMAB-P2109-YC)

Provided herein is a Mouse monoclonal antibody against Human Plasminogen. The antibody can be used for immunoassay techniques, such as WB, IHC-P.
See all PLG antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
10A1
Antibody Isotype
IgG1, κ
Application
WB, IHC-P

Basic Information

Immunogen
Protein purified from Human plasma
Specificity
Human
Antibody Isotype
IgG1, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

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

Format
HEPES with 150 mM sodium chloride, 0.01% BSA, 0.03% sodium azide, and 50% glycerol
Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at-20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
plasminogen
Introduction
PLG is a secreted blood zymogen that is activated by proteolysis and converted to plasmin and angiostatin. Plasmin dissolves fibrin in blood clots and is an important protease in many other cellular processes while angiostatin inhibits angiogenesis. Defects in this gene are likely a cause of thrombophilia and ligneous conjunctivitis.
Entrez Gene ID
5340
UniProt ID
P00747
Alternative Names
Plasminogen; PLG
Function
Plasmin dissolves the fibrin of blood clots and acts as a proteolytic factor in a variety of other processes including embryonic development, tissue remodeling, tumor invasion, and inflammation. In ovulation, weakens the walls of the Graafian follicle. It activates the urokinase-type plasminogen activator, collagenases and several complement zymogens, such as C1 and C5. Cleavage of fibronectin and laminin leads to cell detachment and apoptosis. Also cleaves fibrin, thrombospondin and von Willebrand factor. Its role in tissue remodeling and tumor invasion may be modulated by CSPG4. Binds to cells.
Angiostatin is an angiogenesis inhibitor that blocks neovascularization and growth of experimental primary and metastatic tumors in vivo.
(Microbial infection) ENO/enoloase from parasite P.falciparum (strain NF54) interacts with PLG present in the mosquito blood meal to promote the invasion of the mosquito midgut by the parasite ookinete (PubMed:21949403).
The catalytic active form, plasmin, is essential for the invasion of the mosquito midgut (PubMed:21949403).
Biological Process
Involved in interaction with symbiontManual Assertion Based On ExperimentIDA:CAFA
Blood coagulationManual Assertion Based On ExperimentIMP:HGNC-UCL
Extracellular matrix disassemblyManual Assertion Based On ExperimentIDA:BHF-UCL
FibrinolysisManual Assertion Based On ExperimentIDA:CAFA
Labyrinthine layer blood vessel developmentIEA:Ensembl
Mononuclear cell migrationIEA:Ensembl
Muscle cell cellular homeostasisIEA:Ensembl
Myoblast differentiationIEA:Ensembl
Negative regulation of cell population proliferationManual Assertion Based On ExperimentTAS:ProtInc
Negative regulation of cell-cell adhesion mediated by cadherinManual Assertion Based On ExperimentTAS:BHF-UCL
Negative regulation of cell-substrate adhesionManual Assertion Based On ExperimentIDA:BHF-UCL
Negative regulation of fibrinolysisManual Assertion Based On ExperimentIDA:BHF-UCL
Positive regulation of blood vessel endothelial cell migrationIGI:CAFA
Positive regulation of fibrinolysisManual Assertion Based On ExperimentIDA:AgBase
ProteolysisManual Assertion Based On ExperimentIDA:CAFA
Tissue regenerationIEA:Ensembl
Tissue remodelingIEA:UniProtKB-KW
Trans-synaptic signaling by BDNF, modulating synaptic transmissionIEA:Ensembl
Trophoblast giant cell differentiationIEA:Ensembl
Cellular Location
Secreted
Locates to the cell surface where it is proteolytically cleaved to produce the active plasmin. Interaction with HRG tethers it to the cell surface.
Involvement in disease
Plasminogen deficiency (PLGD):
A disorder characterized by decreased serum plasminogen activity. Two forms of the disorder are distinguished: type 1 deficiency is additionally characterized by decreased plasminogen antigen levels and clinical symptoms, whereas type 2 deficiency, also known as dysplasminogenemia, is characterized by normal, or slightly reduced antigen levels, and absence of clinical manifestations. Plasminogen deficiency type 1 results in markedly impaired extracellular fibrinolysis and chronic mucosal pseudomembranous lesions due to subepithelial fibrin deposition and inflammation. The most common clinical manifestation of type 1 deficiency is ligneous conjunctivitis in which pseudomembranes formation on the palpebral surfaces of the eye progresses to white, yellow-white, or red thick masses with a wood-like consistency that replace the normal mucosa.
Angioedema, hereditary, 4 (HAE4):
A form of angioedema, a disorder characterized by episodic local swelling involving subcutaneous or submucous tissue of the upper respiratory and gastrointestinal tracts, face, extremities, and genitalia. HAE4 is an autosomal dominant form with incomplete penetrance, variable expressivity, and female predominance.
PTM
N-linked glycan contains N-acetyllactosamine and sialic acid. O-linked glycans consist of Gal-GalNAc disaccharide modified with up to 2 sialic acid residues (microheterogeneity).
In the presence of the inhibitor, the activation involves only cleavage after Arg-580, yielding two chains held together by two disulfide bonds. In the absence of the inhibitor, the activation involves additionally the removal of the activation peptide.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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