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Coagulation Factor VIII (F8) ELISA Kits

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. Additionally we are shipping Factor VIII Antibodies (341) and Factor VIII Proteins (26) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
F8 14069 Q06194
F8 2157 P00451
F8 302470  
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Top Factor VIII ELISA Kits at antibodies-online.com

Showing 10 out of 45 products:

Catalog No. Reactivity Sensitivity Range Images Quantity Supplier Delivery Price Details
Human 30pg/mL 78-5.000 pg/mL 96 Tests Log in to see 9 to 11 Days
$700.00
Details
Mouse 0.275 ng/mL 6.25-400 pg/mL 96 Tests Log in to see 9 to 11 Days
$720.00
Details
Dog 2.39 ng/mL 15.63-1000 pg/mL 96 Tests Log in to see 9 to 11 Days
$800.00
Details
Pig
  96 Tests Log in to see 8 to 9 Days
$770.00
Details
Rabbit
  96 Tests Log in to see 8 to 9 Days
$770.00
Details
Chicken
  96 Tests Log in to see 8 to 9 Days
$770.00
Details
Monkey
  96 Tests Log in to see 8 to 9 Days
$770.00
Details
Rat
5-100 ng/mL   96 Tests Log in to see 11 to 13 Days
$785.71
Details
Human
  96 Tests Log in to see 2 to 3 Days
$350.00
Details
Goat
  96 Tests Log in to see 11 to 13 Days
$801.43
Details

More ELISA Kits for Factor VIII Interaction Partners

Zebrafish Coagulation Factor VIII (F8) interaction partners

  1. gene is flanked by factor VII (show TH ELISA Kits) and factor X genes; gene encodes a protein homologous to factor VII (show TH ELISA Kits), but lacks critical residues for factor VII (show TH ELISA Kits) 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. data demonstrate that infusion of platelets containing FVIII triggers neither primary nor memory anti-FVIII immune response in FVIII(null) mice

  2. Both platelet-VWF (show VWF ELISA Kits) and plasma-VWF (show VWF ELISA Kits) are required for optimal platelet-derived FVIII gene therapy for hemophilia A in the presence of inhibitors.

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

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

  5. This study demonstrated that FVIIIa interacts with Low-density lipoprotein receptor-related protein 1 (show LRP1 ELISA Kits) cluster III.

  6. a fragment containing only approximately 20% of the VWF (show VWF ELISA Kits) sequence is sufficient to support FVIII stability in vivo

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

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

  9. Micro-computed tomography analysis of distal tibia metaphyses also revealed for the first time a major impact of the FVIII/thrombin (show F2 ELISA Kits)/PAR1 (show F2R ELISA Kits) axis on the dynamic bone structure, showing reduced bone.

  10. 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.

Human Coagulation Factor VIII (F8) interaction partners

  1. Letter: report deep intronic variants of factor VII (show TH ELISA Kits) gene in hemophilia A.

  2. Coagulation test results showed that the presence of double Glu113Asp, Arg593Cys mutations has a slightly synergistic effect on FVIII activity.

  3. Report a dose-response relationship between high FVIII levels and risk of death in venous thrombosis patients and in individuals from the general population.

  4. Case Report: P1809L mutation in A3 induced the conformational change in the FVIII molecule that hampered antigenic determinant(s) located in the C2 domain and might result in the inhibitor development.

  5. FVIII predicted venous thrombosis recurrence in a dose-response fashion, overall and in several subgroups, and is a strong candidate component of recurrence prediction tools.

  6. Interaction between VWF (show VWF ELISA Kits) and FVIII in treating VWD (show VWF ELISA Kits).

  7. a grading system for FVIII mutations combining the severity determinants was developed and the grading pattern correlates with hemophilia phenotype, is reported.

  8. Among the seven HA families whose coding region of the FVIII gene was directly sequenced,five patients and certain of their female relatives had mutations detected.

  9. Stimulated GMVECs and HUVECs were found to secrete cell-anchored ultra-large VWF (show VWF ELISA Kits) strings covered with bound FVIII.

  10. Association between micro particle-tissue factor (show F3 ELISA Kits) activity, factor VIII activity and recurrent VTE in patients with acute pulmonary embolism.

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

  1. thrombin (show F2 ELISA Kits) stimulates transglutaminase activity in articular cartilage by directly cleaving factor XIII (show UGDH ELISA Kits) and by receptor-mediated up-regulation of factor XIII (show UGDH ELISA Kits) synthesis

  2. 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. Factor VIIIc (show COX7A2 ELISA Kits) is responsible for tissue invasion during tumor progression.

Factor VIII (F8) Antigen Profile

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) ELISA Kits

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

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

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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