Coagulation Factor VIII (F8) Kits ELISA

F8 encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation\; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. De plus, nous expédions Factor VIII Anticorps (324) et Factor VIII Protéines (24) et beaucoup plus de produits pour cette protéine.

list all ELISA KIts Gène GeneID UniProt
F8 14069 Q06194
F8 2157 P00451
F8 302470  
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Top Factor VIII Kits ELISA sur anticorps-enligne.fr

Showing 10 out of 61 products:

Catalogue No. Reactivité Sensibilité Gamme Images Quantité Fournisseur Livraison Prix Détails
Chien 31.25 ng/mL 125-8000 ng/mL Typical standard curve 96 Tests Connectez-vous pour afficher 15 to 18 Days
$1,026.67
Détails
Humain 30 pg/mL 78 pg/mL - 5000 pg/mL 96 Tests Connectez-vous pour afficher 13 to 16 Days
$700.00
Détails
Souris 0.273 ng/mL 0.62 ng/mL - 40 ng/mL 96 Tests Connectez-vous pour afficher 13 to 16 Days
$720.00
Détails
Rat 4.688 pg/mL 7.813-500 pg/mL Typical standard curve 96 Tests Connectez-vous pour afficher 12 to 14 Days
$638.00
Détails
Porc
  96 Tests Connectez-vous pour afficher 2 to 3 Days
$867.90
Détails
Lapin 18.75 pg/mL 31.25-2000 pg/mL   96 Tests Connectez-vous pour afficher 12 to 14 Days
$616.00
Détails
Singe 0.188 ng/mL 0.313-20 ng/mL   96 Tests Connectez-vous pour afficher 12 to 14 Days
$616.00
Détails
Poulet 0.188 ng/mL 0.313-20 ng/mL   96 Tests Connectez-vous pour afficher 12 to 14 Days
$616.00
Détails
Humain 30 pg/mL 78 pg/mL - 5000 pg/mL   96 Tests Connectez-vous pour afficher 8 to 12 Days
$928.46
Détails
Souris 2.64 pg/mL 6.25 pg/mL - 400 pg/mL   96 Tests Connectez-vous pour afficher 8 to 12 Days
$951.54
Détails

Factor VIII Kits ELISA mieux référencés

  1. Human Factor VIII Kit ELISA pour Sandwich ELISA - ABIN456987 : Wang, Yuan, Zhong, Wen, Deng, Liang, Zheng: The anticoagulant effect of PGI2S and tPA in transgenic umbilical vein endothelial cells is linked to up-regulation of PKA and PKC. dans International journal of molecular sciences 2014 (PubMed)
    Show all 2 Pubmed References

Plus Kits ELISA pour Factor VIII partenaires d'interaction

Zebrafish Coagulation Factor VIII (F8) interaction partners

  1. gene is flanked by factor VII and factor X genes; gene encodes a protein homologous to factor VII, but lacks critical residues for factor VII activity; functions as an inhibitor of blood coagulation in biochemical assays using zebrafish or human plasmas

Mouse (Murine) Coagulation Factor VIII (F8) interaction partners

  1. Haemophilic animals (F8(-/-) mice) fed a high fat/fructose diet are highly prone to hepatic steatosis and thrombocytopenia.

  2. CD32 blockade suppresses the FVIII-specific recall response by two ways: i) increasing apoptosis of FVIII-specific memory B-cells and ii) disturbing FVIII-specific T cell response by modulating presentation of rhFVIII to CD4(+) T cells.

  3. Type 2N von Willebrand disease variants were associated with decreased VWF secretion and impaired factor VIII binding/stability.

  4. Cytokine release was quantified from FVIII(-/-) splenocytes restimulated with FVIII in the absence or presence of different anti-FcgammaRIIB (CD32) Antibodies (anti-CD32 mAbs) over 6 days.

  5. results revealed localized vascular expression of FVIII and von Willebrand factor and identified lymphatic endothelial cell as a major cellular source of FVIII in extrahepatic tissues.

  6. the results indicate that residues in the C1 and/or C2 domains of factor VIII are implicated in immunogenic factor VIII uptake, at least in vitro Conversely, in vivo, the binding to endogenous von Willebrand factor masks the reducing effect of mutations in the C domains on factor VIII immunogenicity.

  7. Describe a genetically engineered mouse model of hemophilia A with complete deletion of the F8 gene.

  8. data demonstrate that infusion of platelets containing FVIII triggers neither primary nor memory anti-FVIII immune response in FVIII(null) mice

  9. Both platelet-VWF and plasma-VWF are required for optimal platelet-derived FVIII gene therapy for hemophilia A in the presence of inhibitors.

  10. These data support the investigation of FVIII orthologs as treatment modalities in both the congenital and acquired FVIII inhibitor settings.

  11. Extrahepatic sources of factor VIII potentially contribute to the coagulation cascade correcting the bleeding phenotype of mice with hemophilia A.

  12. Activatable bioengineered FIX molecules with FVIII-independent activity might be a promising tool for improving hemophilia A treatment, especially for patients with inhibitors.

  13. This study demonstrated that FVIIIa interacts with Low-density lipoprotein receptor-related protein 1 cluster III.

  14. a fragment containing only approximately 20% of the VWF sequence is sufficient to support FVIII stability in vivo

  15. Endothelial cells from multiple, but not all, tissues contribute to the plasma FVIII pool in the mouse.

  16. Endothelial cells are the predominant, and possibly exclusive, source of plasma FVIII.

  17. Micro-computed tomography analysis of distal tibia metaphyses also revealed for the first time a major impact of the FVIII/thrombin/PAR1 axis on the dynamic bone structure, showing reduced bone.

  18. Findings indicate that improving protein trans-splicing by inter-chain disulfide bonding is a promising approach for increasing the efficacy of dual-vector based FVIII gene transfer.

  19. Acute elevations in FVIII levels result in a non-linear thrombogenic effect, with non-significant increases in thrombogenic risk. Prolonged elevation of plasma FVIII did not further increase the thrombogenic potential of elevated FVIII levels.

  20. Transient B cell depletion and even more so use of a codon-optimized FVIII sequence in hepatic gene transfer represent promising strategies to avoid inhibitor formation and promote tolerance in gene therapy for hemophilia A.

Human Coagulation Factor VIII (F8) interaction partners

  1. This study describes an original pathological mechanism by which a small intronic deletion in F8 leads to Alu exonization.

  2. A common polymorphism decreases LRP1 mRNA stability and is associated with increased plasma factor VIII levels

  3. F8 and F9 gene variants result from a founder effect in two large French haemophilia cohorts

  4. our results demonstrate that the N-glycosylation sequon in the A2 domain is located in a structural element that is critically required for proper folding and conformation of FVIII.

  5. The aim of this study was to determine the F8 mutations in severe HA (sHA) patients and female carriers

  6. Human FVIII gene transfer without in vivo selection of manipulated cells can introduce immune tolerance in hemophilia A mice and this immune tolerance is CD4(+) T cell mediated.

  7. In Factor VIII, 41 mutations were identified, 19 of which were novel and 80% (44/55) of the pathogenic mutations fell into the categories of missense, nonsense(16.36%), frameshift (14.55%), and splice (5.45%) mutations.

  8. High dose of rhFVIII induces apoptosis in FVIII-specific memory B-cells but does not influence FVIII-specific T cell response.

  9. the potential role of FXIII-A in wound healing, as a field with long-term therapeutic implications, is also discussed

  10. Case Report: complex recombination with deletion in the F8 and duplication in the TMLHE mediated by int22h copies during early embryogenesis in proband's mother.

  11. Report a diagnostic algorithm that can reliably identify pathogenic variants of factor 8/9 and von Willebrand factor and diagnose patients with hemophilia A, hemophilia B or von Willebrand disease.

  12. Each hFVIII vector was administered to FVIII knockout (KO) mice at a dose of 10(10) genome copies (GC) per mouse. Criteria for distinguishing the performance of the different enhancer/promoter combinations were established prior to the initiation of the studies.

  13. Relevance of ethnic differences in factor XIII activity on laboratory reference ranges.

  14. analysis of co-existing variants in both F8 and PTGS-1 genes in a three-generation pedigree of hemophilia A

  15. Potential mutations of the F8 gene were analyzed.

  16. FVIII endocytosis is driven by interaction with LRP1

  17. A coagulation initiating pathway is revealed in which the TF-FVIIa-nascent FXa complex activates FVIII apart from thrombin feedback.

  18. An in silico and in vitro approach to elucidate the impact of residues flanking the cleavage scissile bonds of FVIII by thrombin has been presented.

  19. Of special importance is the sequential formation of disulfide bonds with different functions in structural support of VWF multimers, which are packaged, stored and further processed after secretion. Here, all these processes are being reviewed in detail including background information on the occurring biochemical reactions. [review]

  20. The FVIII C1 domain contributes significantly to the immune response against FVIII in acquired and congenital hemophilia inhibitor patients.

Pig (Porcine) Coagulation Factor VIII (F8) interaction partners

  1. It was concluded that VEGF and factor VIII are important growth factors associated with fetal development in pigs and are identified in all uterine segments.

  2. Report Factor VIII organisation on nanodiscs with different lipid composition.

  3. thrombin stimulates transglutaminase activity in articular cartilage by directly cleaving factor XIII and by receptor-mediated up-regulation of factor XIII synthesis

  4. cupredoxin-like A1 subdomains in fVIII contain inter-species differences that are a result of selective pressure on the dissociation rate constant

Cow (Bovine) Coagulation Factor VIII (F8) interaction partners

  1. two factor VIII missense mutations are associated with a mild form of haemophilia A in German Fleckvieh cattle

  2. Factor VIIIc is responsible for tissue invasion during tumor progression.

  3. A missense mutation (p.Leu2153His) of the factor VIII gene causes cattle haemophilia A.

Factor VIII (F8) profil antigène

Antigen Summary

This gene encodes coagulation factor VIII, which participates in the intrinsic pathway of blood coagulation\; factor VIII is a cofactor for factor IXa which, in the presence of Ca+2 and phospholipids, converts factor X to the activated form Xa. This gene produces two alternatively spliced transcripts. Transcript variant 1 encodes a large glycoprotein, isoform a, which circulates in plasma and associates with von Willebrand factor in a noncovalent complex. This protein undergoes multiple cleavage events. Transcript variant 2 encodes a putative small protein, isoform b, which consists primarily of the phospholipid binding domain of factor VIIIc. This binding domain is essential for coagulant activity. Defects in this gene results in hemophilia A, a common recessive X-linked coagulation disorder.

Gene names and symbols associated with Coagulation Factor VIII (F8) Kits ELISA

  • coagulation factor VIIi (f7i) anticorps
  • coagulation factor VIII (F8) anticorps
  • coagulation factor VIII, procoagulant component (F8) anticorps
  • AHF anticorps
  • Cf-8 anticorps
  • Cf8 anticorps
  • DXS1253E anticorps
  • F8B anticorps
  • F8C anticorps
  • fb61d02 anticorps
  • FVIII anticorps
  • HEMA anticorps
  • wu:fb61d02 anticorps

Protein level used designations for Coagulation Factor VIII (F8) Kits ELISA

Factor VIII , procoagulant component , antihemophilic factor , coagulation factor VIII , coagulation factor VIIIc , factor VIII F8B , coagulation factor VIII, procoagulant component (hemophilia A) , factor VIII , coagulation co-factor

GENE ID SPECIES
282671 Danio rerio
14069 Mus musculus
2157 Homo sapiens
397339 Sus scrofa
403875 Canis lupus familiaris
100271720 Bos taurus
100303761 Oryctolagus cuniculus
302470 Rattus norvegicus
100359363 Ovis aries
422199 Gallus gallus
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