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Factor V Antibody (2280A) [DyLight 405]

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Product Details

Summary
Reactivity HuSpecies Glossary
Applications ELISA, CyTOF-ready, Flow
Clone
2280A
Clonality
Monoclonal
Host
Rabbit
Conjugate
DyLight 405

Order Details

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Factor V Antibody (2280A) [DyLight 405] Summary

Additional Information
Recombinant Monoclonal Antibody
Immunogen
Synthetic peptide containing human Coagulation Factor V aa1650-1700
Accession # P12259
Specificity
Detects human Coagulation Factor V in direct ELISAs.
Isotype
IgG
Clonality
Monoclonal
Host
Rabbit
Purity
Protein A or G purified from cell culture supernatant
Innovator's Reward
Test in a species/application not listed above to receive a full credit towards a future purchase.

Applications/Dilutions

Dilutions
  • CyTOF-ready
  • ELISA
  • Intracellular Staining by Flow Cytometry
Application Notes
Optimal dilution of this antibody should be experimentally determined.

Packaging, Storage & Formulations

Storage
Store at 4C in the dark.
Buffer
50mM Sodium Borate
Preservative
0.05% Sodium Azide
Purity
Protein A or G purified from cell culture supernatant

Notes

DyLight (R) is a trademark of Thermo Fisher Scientific Inc. and its subsidiaries.

Alternate Names for Factor V Antibody (2280A) [DyLight 405]

  • Activated protein C cofactor
  • Cf5
  • Cf-5
  • Coagulation Factor 5
  • coagulation factor V (proaccelerin, labile factor)
  • coagulation factor V jinjiang A2 domain
  • Coagulation Factor V
  • F5
  • factor V Leiden
  • Factor V
  • FVL
  • PCCF
  • Proaccelerin, Labile Factor
  • RPRGL1
  • THPH2

Background

The F5 gene encodes a 2,224 amino acid long, 251 kDA coagulation factor V protein that is critical in the regulation of homeostasis. Additionally, F5 functions as a cofactor for the prothrombinase activity of factor Xa which results in the initiation of prothrombin to thrombin. F5 participates in blood coagulation signaling pathways, the blood clotting cascade, platelet degranulation as well as activation, signaling, and aggregation, and in responses to elevated platelet cytosolic Ca2+. It interacts with genes PROC, PROS1, F2, MMRN1, and CALR. Defects in F5 cause factor 5 deficiency (owren parahemophilia), thrombophilia due to activated protein C resistance, susceptibility to Budd-Chiari syndrome, susceptibility to ischemic strokes, and susceptibility to pregnancy loss, recurrent, type 1. F5 is also linked to deep vein thrombosis, antithrombin III deficiency, retinal vein occlusion, legg-calve-perthes disease, liver disease, hypertension, pulmonary embolism, lupus, and patent foramen ovale.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Isotype Controls

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