SKU: WM1301 Categories: ,

CD141 [ABT145] mouse mAb

Price range: $268.00 through $328.00

SKU: WM1301-50
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Product details

Background:
CD141 is a 75 kDa transmembrane glycoprotein expressed in many normal tissues, such as arterial and venous endothelial cells and mesothelial cells. CD141 is not expressed in liver adenocarcinoma. CD141 protein is a sensitive marker of lymphatic endothelial cells and their tumors. It can be used to distinguish lung adenocarcinoma from malignant mesothelioma.

Specifications

Size50μL/100μL
TargetCD141
ReactivityHuman, Mouse, Rat
ApplicationsIHC, WB, IF, ELISA
MW(Calculated)62kD
MW(Observed)100kD
Host SpeciesMouse
IsotypeIgG2b,Kappa
Conjugate/ModificationUnmodified
Recommended Dilution RatioIHC 1:200-1000; WB 1:500-2000; IF 1:100-500; ELISA 1:1000-5000 / Note: For IHC, we suggest antigen retrieval with TE buffer pH 9.0 (Cat#WT1004)
FormulationPBS, 50% glycerol, 0.05% Proclin 300, 0.05%BSA
PurificationRecombinant Antibody expressed in animal component-free (ACF) media, purified via Protein G affinity chromatography.
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone NumberRMM145
ImmunogenSynthesized peptide derived from human CD141 AA range: 50-150
SpecificityThe antibody can specifically recognize human CD141 protein.
Gene NameTHBD THRM
Protein NameCD141
Other NameAHUS 6; / AHUS6; / BDCA 3; / BDCA3; / CD 141; / CD141; / CD141 antigen; / Fetomodulin; / Thbd; / THPH12; / THRM; / Thrombomodulin; / TM; / TRBM_HUMAN
SpeciesHuman
Gene ID7056
UniprotP07204
Species.1
Gene ID.1
Uniprot.1
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationMembranous
Tissue ExpressionEndothelial cells are unique in synthesizing thrombomodulin.
Signaling_pathwayOrganismal Systems >> Immune system >> Complement and coagulation cascades
Research Areas>>Complement and coagulation cascades; / >>AGE-RAGE signaling pathway in diabetic complications; / >>Fluid shear stress and atherosclerosis
FunctionDisease:Defects in THBD are the cause of thrombophilia due to thrombomodulin defect (THR-THBDD) [MIM:188040]. THR-THBDD is a hemostatic disorder characterized by a tendency to thrombosis.,Function:Thrombomodulin is a specific endothelial cell receptor that forms a 1:1 stoichiometric complex with thrombin. This complex is responsible for the conversion of protein C to the activated protein C (protein Ca). Once evolved, protein Ca scissions the activated cofactors of the coagulation mechanism, factor Va and factor VIIIa, and thereby reduces the amount of thrombin generated.,online information:Thrombomodulin,online information:Thrombomodulin entry,PTM:N-glycosylated.,PTM:The iron and 2-oxoglutarate dependent 3-hydroxylation of aspartate and asparagine is (R) stereospecific within EGF domains.,similarity:Contains 1 C-type lectin domain.,similarity:Contains 6 EGF-like domains.,tissue specificity:Endothelial cells are unique in synthesizing thrombomodulin.,
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