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F2145

Sigma-Aldrich

Monoclonal Anti-Factor V antibody produced in mouse

clone HV-1, purified immunoglobulin, buffered aqueous solution

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.43

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

HV-1, monoclonal

form

buffered aqueous solution

species reactivity

human

technique(s)

ELISA: suitable
dot blot: suitable
neutralization: suitable

isotype

IgG1

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

human ... F5(2153)

General description

Monoclonal Anti-Factor V (mouse IgG1 isotype) is derived from the HV-1 hybridoma, produced by the fusion of mouse myeloma Sp2/0-Ag14 cells and splenocytes from BALB/c mouse immunized with Factor V, purified from human plasma. Blood coagulation factor V, also known as, proaccelerin or labile factor. The activated factor V (factor Va) is a calcium dependent heterodimer composed of heavy chain (~105 kDa) and light chain (~73 kDa).

Specificity

The antibody inhibits the activity of Factor V as measured by the prothrombin time (PT) assay.

Immunogen

Factor V from pooled normal human plasma

Application

Monoclonal Anti-Factor V antibody produced in mouse has been used in dot blot and enzyme linked immunosorbent assay (ELISA).

Biochem/physiol Actions

Blood coagulation factor V is an essential component of the prothrombinase complex that catalyzes the rapid conversion of prothrombin to thrombin and is involved in intrinsic and extrinsic coagulation pathways. About 20% of blood factor V is contained within platelets. Factor V circulates in the plasma as a single chain glycoprotein with little or no intrinsic procoagulant activity. It is activated through limited proteolysis by thrombin, factor Xa, or the factor V activator from Russell′s viper venom (RW-V). Activated protein C (APC) with its cofactor protein S, inactivates factors Va and VIIIa to provide a major natural anticoagulant system. APC resistance known as factor V Leiden (FV Leiden) is a common hereditary thrombophilia Factor V mutation, caused by arginine substitution into glutamine at position 506 (R506Q).

Physical form

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 15 mM sodium azide as a preservative.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Storage Class Code

10 - Combustible liquids

WGK

WGK 2

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Platelet factor V to the rescue
Camire RM, et al.
Blood, 115(4), 753-754 (2010)
Overview of the coagulation system
Palta S, et al.
Indian journal of anaesthesia, 58(5), 515-515 (2014)
Factor V Leiden and Inflammation
Perez-Pujol S, et al.
Thrombosis, 2012 (2012)
Blood coagulation factors V and VIII: Molecular Mechanisms of Procofactor Activation
Bos MHA and Camire RM
Journal of coagulation disorders., 2(2), 19-19 (2010)

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