Human thrombomodulin,TM ELISA Kit

Code CSB-E07937h
Size 96T,5×96T,10×96T
Price Request a Quote or Start an on-line Chat
Trial Size 24T ELISA Kit Trial Size (Only USD$150/ kit)
* The sample kit cost can be deducted from your subsequent orders of 96T full size kits of the same analyte at 1/5 per kit, until depleted in 6 months. Apply now

Product Details

Target Name
thrombomodulin
Alternative Names
THBD; THRM; Thrombomodulin; TM; Fetomodulin; CD antigen CD141
Abbreviation
THBD
Uniprot No.
Species
Homo sapiens (Human)
Sample Types
serum, plasma, tissue homogenates
Detection Range
0.312 ng/mL-20 ng/mL
Sensitivity
0.078 ng/mL
Assay Time
1-5h
Sample Volume
50-100ul
Detection Wavelength
450 nm
Research Area
Cardiovascular
Assay Principle
quantitative
Measurement
Sandwich
Precision

Typical Data

Troubleshooting
and FAQs
Storage
Store at 2-8°C. Please refer to protocol.
Lead Time
3-5 working days after you place the order, and it takes another 3-5 days for delivery via DHL or FedEx
Description

This Human THBD ELISA Kit was designed for the quantitative measurement of Human THBD protein in serum, plasma, tissue homogenates. It is a Sandwich ELISA kit, its detection range is 0.312 ng/mL-20 ng/mL and the sensitivity is 0.078 ng/mL.

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 Q&A
Q:

Please I need a quotation for this devices with this specifications:product name:human soluble thrombomodulin ELISA kit,solid phases sandwiches ELISA,sample type:serum,volume required:10ul of serum,sensitivity:<10pg/ml,specificity:natural human soluble thrombomodulin,pack size:96 wells/kit polystyrene microplate (12 strips of 8 well) coated with a monoclonal antibody specific for natural human soluble thrombomodulin,assay range:62.5-4.000 pg/ml

A:
Thanks for your enquiry. I will send you the kit manual and the contact information of distributor in your area by email.
If any questions,pls let me know.
Q:

If the human Thrombomodulin ELISA kit (https://www.cusabio.com/ELISA-Kit/Human-thrombomodulin-TM-ELISA-Kit-108098.html) detects soluble Thrombomodulin fragments, or just the integral plasma membrane Thrombomodulin, or both?

A:
Thanks for your inquiry.
CSB-E07937h is designed according to this information: https: / / www.uniprot.org / uniprot / P07204.
It detects the soluble thrombomodulin.
And dear, even if the integral plasma membrane is under the case of physical or mechanical forces, it will be converted as soluble form.
So this kit actually can detect both of the forms.

Target Background

Function
(From Uniprot)
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.
Gene References into Functions
  1. Thrombomodulin gene C1418T polymorphism is associated with Kawasaki disease. PMID: 30008974
  2. SETD1A contributes to retinoic acid -induced thrombomodulin expression in vascular endothelial cells by modulating the activity and expression of KLF4. PMID: 29940355
  3. we for the first time demonstrated that TM binds to GPR15 via its EGF-like domain and exerts angiogenesis and cytoprotective function in vascular ECs. PMID: 28386128
  4. Bioinformatics analysis and screening of controls strongly suggested that the THBD-p.Trp153Gly mutation might be related to RPL aetiology. PMID: 29195508
  5. Taken together, our findings suggest that TM-PKCdelta interaction may contribute to cardiovascular disorders by affecting monocye differentiation, which may develop future therapeutic applications. PMID: 27910925
  6. A heterozygous variant displaying autosomal dominant inheritance (c.1611 C>A) was found in the gene THBD which encodes the glycoprotein thrombomodulin. This sequence change results in a stop codon (p.Cys537Stop) and truncation of the protein PMID: 28267383
  7. Lys 42, Lys 43, Lys 44 and Arg 12 are critical for the interaction of TAFI with the thrombin-thrombomodulin complex, which modulates its antifibrinolytic potential. PMID: 28640323
  8. Ligation of anti-HLA class I and II antibodies produces different effects on the endothelial expression of TBM and on serum levels of TBM in transplant recipients. PMID: 28239987
  9. Fibrinogen gamma acts as thrombomodulin II. (Review) PMID: 27784620
  10. Thrombomodulin (TM) promotes angiogenesis by enhancing cell adhesion, migration, and FAK activation through interaction with fibronectin. PMID: 27602495
  11. The elevation of serum thrombomodulin (sTM)level suggests that endothelial damage occurs in Abdominal Aortic Aneurysm pathogenesis. PMID: 28473982
  12. This population-based cohort study within the ARIC study did not replicate the Hernandez et al. finding that carrying the minor allele of 3 THBD SNPs doubles the risk of venous thromboembolism in African Americans. In fact, the HRs of VTE among carriers of the minor allele were <1. HRs were similar for white subjects. A strand-flip did not explain the discrepancies. PMID: 28619983
  13. these results suggest a novel function for thrombomodulin as an adhesion molecule in monocytes, where it enhances cell adhesion by binding Ley, leading to beta2 integrin activation via p38 MAPK PMID: 27808085
  14. TM, especially TME45, maintains vascular integrity, at least in part, via Src signaling. PMID: 27643869
  15. The present study found that the fifth epidermal growth factor-like domain of thrombomodulin (TME5) possesses the cytoprotective function in association with an increase in levels of anti-apoptotic myeloid cell leukemia-1 protein in an activated protein C-independent PMID: 27427915
  16. Case Report: CD141+ myeloid dentritic cell differentiation of a juvenile myelomonocytic leukemia. PMID: 28414089
  17. the effect of thromobomodulin c.1418C > T polymorphism on the pathogenesis of venous thrombosis PMID: 28710034
  18. The finding of a previously unrecognized fibrinolytic phenotype indicates that bleeding in Thrombomodulin-associated coagulopathy has a complex pathogenesis and highlights the pivotal role of TM as a regulator of hemostasis. PMID: 27436851
  19. TM mediates cell proliferation and migration via the Epithelial-To-Mesenchymal Transition (EMT) biomarkercyclooxygenase (COX)-2 PMID: 27512995
  20. the whole THBD gene sequenced in patients with recurrent venous thromboembolism (VTE); found 8 polymorphisms in the THBD gene in Swedish population; none of these polymorphisms was significantly associated with the risk of VTE recurrence; results indicate that THBD polymorphisms may not be a risk factor for VTE recurrence PMID: 28049360
  21. CORM-2 protects human umbilical vein endothelial cells from lipopolysaccharide-induced injury, by way of suppressing NF-kappaB activity, which downregulates TM and EPCR mRNAs. It also decreases MMP-2 expression and prevents the shedding of TM and EPCR from the surface of endothelial cells, so as to preserve their protective effect. PMID: 28538400
  22. The results demonstrate that the LFA-1 and Mac-1 integrins on leukocytes bind to thrombomodulin (TM), thereby establishing the molecular and structural basis underlying LFA-1 and Mac-1 integrin interaction with TM on endothelial cells. PMID: 27055590
  23. Human thrombomodulin transgenic aortic endothelial cells are less sensitive to activation by either HMGB1 or hTNFalpha, an effect that appears to be dependent on the lectin-like domain of TBM. PMID: 27077599
  24. In placenta of patients with preeclampsia, we detected abnormal expression of F3 and THBD with increased protein and mRNA levels. The role of these molecules in the pathogenesis of this disease and in alterations of hemostatic and histopathological aspects of placentas need further studying. PMID: 27002259
  25. recombinant TM (Solulin) can protect the intestine from toxicity in a clinically relevant rat model PMID: 27459702
  26. TM up-regulated E-cadherin but down-regulated N-cadherin expression, resulting in reversal of epithelial-mesenchymal transition (EMT) in the lung cancer cells. PMID: 27223053
  27. High serum thrombomodulin expression is associated with non-alcoholic fatty liver disease. PMID: 26959535
  28. results do not suggest a predictive role for THBD c.1418C>T polymorphism in VTE recurrence PMID: 26743062
  29. R12 is a critical residue for the activation of TAFI by thrombin-thrombomodulin PMID: 26816270
  30. Study detected a statistically significant positive correlation between expanded disability status scale scores and thrombomodulin levels (p<0.01) and a 10% positive correlation between expanded disability status scale scores and APC levels in multiple sclerosis patients PMID: 27456888
  31. Case Report: thrombotic microangiopathy with mutations in complement factor I and thrombomodulin. PMID: 26613809
  32. increased plasma TM levels and serum hs-CRP levels in cerebral infarction (CI) patients were associated with the development of CI in Asians. PMID: 26133301
  33. evidence of association between the -33G/A polymorphism in the TM gene and the risk of myocardial infarction in Asians; the Ala455Val variant was not associated with atherosclerotic risk [meta-analysis] PMID: 26888356
  34. Decreased thrombomodulin expression in preeclampsia may play a role in placental dysfunction in preeclampsia and is possibly caused by an angiogenic imbalance. Hypertension and obesity are associated with thrombomodulin downregulation. PMID: 26891741
  35. The presence of THBD proximal promoter polymorphisms do not explain variations in levels of serum and cell-expressed THBD in premature acute coronary syndrome patients in Bahrain. PMID: 26226255
  36. the functional relevance of the rs3176123 variation and indicate that higher thrombomodulin expression by individuals with the 2729C allele likely accounts for their decreased risk for acute GVHD development and subsequent mortality. PMID: 26246110
  37. The lack of any association between the sTM levels and genetic variants in ARDS suggests that the increased levels of sTM may reflect severity of endothelial damage rather than genetic heterogeneity. PMID: 25643902
  38. Identified Nur77/Nor1 as novel regulators of thrombomodulin expression and function in vascular endothelial cells. PMID: 26634653
  39. The results of this study supported the association of the epistatic interactions of ALOX5AP, THBD, and KNG1 and present novel evidence for the main effect of KNG1 gene on IS susceptibility. PMID: 26159646
  40. The EGF5, 6 domains of thrombomodulin appear to be the major domains for down-regulating the complement system rather than the lectin-like domain during xenogenic stimuli. PMID: 26179123
  41. A minimal TM fragment consisting of the fourth, fifth, and most of the sixth EGF-like domain (TM456m) that has been prepared has much improved solubility, thrombin binding capacity, and anticoagulant activity versus those of previous TM456 constructs. PMID: 26468766
  42. Data indicate that blood dendritic cell antigen 3 BDCA3(+) and C-type lectin domain family 9, member A CLEC9A(+) dendritic cells (DC) are of major importance in the induction of anti-viral and anti-tumor immunity. PMID: 24910448
  43. Recombinant thrombomodulin does not impair neutrophil functions. PMID: 25214376
  44. levels of protein C and soluble thrombomodulin in critically ill patients with acute kidney injury PMID: 25790110
  45. Membrane-bound TM in macrophages plays an essential role in the development of abdominal aortic aneurysms by enhancing proinflammatory mediator elaboration, macrophage recruitment, and oxidative stress. PMID: 26338301
  46. Cyclic strain strongly downregulated TM expression in a p38- and receptor tyrosine kinase-dependent manner in aortic endothelial cells. PMID: 25238231
  47. kinetics of the interaction between serine/threonine-rich domain of thrombomodulin (rTMD23) and FGFR1 were analysed in umbilical vein endothelial cells PMID: 25388665
  48. Thrombomodulin is differentially regulated within cultured brain microvascular endothelial cells by cytokines and shear stress. PMID: 25250518
  49. Review/Meta-analysis: TM -33G/A and Ala455Val polymorphisms were risk factors for coronary artery disease. PMID: 25144670
  50. function and regulation of BDCA3 expression and IFN-lambda production by dendritic cells PMID: 25616220

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Involvement in disease
Thrombophilia due to thrombomodulin defect (THPH12); Hemolytic uremic syndrome atypical 6 (AHUS6)
Subcellular Location
Membrane; Single-pass type I membrane protein.
Tissue Specificity
Endothelial cells are unique in synthesizing thrombomodulin.
Database Links

HGNC: 11784

OMIM: 188040

KEGG: hsa:7056

STRING: 9606.ENSP00000366307

UniGene: Hs.2030

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