Factor 10 Polyclonal Antibody, ALEXA FLUOR¨ 350 Conjugated


Factor 10 Polyclonal Antibody, ALEXA FLUOR¨ 350 Conjugated

  • Size: 100ul
  • Application: IF(IHC-P)
  • Reactivity: Human, Mouse, Rat
  • Predicted Reactivity:

  • Datasheet      Tech Support


Catalog# bs-9501R-A350

Size:100ul Datasheet


 SizePrice
 100ul ₹ 44220

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PRODUCT DETAILS






SPECIFICATIONS

PRODUCT NAME

Factor 10 Polyclonal Antibody, ALEXA FLUOR¨ 350 Conjugated

CONJUGATION

ALEXA FLUOR¨ 350

HOST

Rabbit

SOURCE

KLH conjugated synthetic peptide derived from human Activated factor Xa heavy chain

IMMUNOGEN RANGE

CLONALITY

Polyclonal

ISOTYPE

IgG

CONCENTRATION

1ug/ul

PURIFICATION

Purified by Protein A.

STORAGE BUFFER

Aqueous buffered solution containing 1% BSA, 50% glycerol and 0.09% sodium azide.

STORAGE CONDITION

Store at 4°C for 12 months.


TARGET

GENE ID

2159

SUBCELLULAR LOCATION

SYNONYMS

Activated factor Xa heavy chain; Coagulation factor; Coagulation factor X; EC 3.4.21.6; F10 antibody FA10_HUMAN; Factor Xa; FX; FXA; OTTHUMP00000018735; Prothrombinase; Stuart factor; Stuart Prower factor; Stuart-Prower factor; Coagulation factor X; Factor X heavy chain.

BACKGROUND

Hemostasis following tissue injury involves the deployment of essential plasma procoagulants (Prothrombin and Factors X, IX, V and VIII), which are involved in a blood coagulation cascade that leads to the formation of insoluble Fibrin clots and the promotion of platelet aggregation. Coagulation Factor X (Stuart Prower factor, FX, F10) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor. The mature form of Factor X (Factor X A) is generated by Factor IX A- or Factor VII A-mediated cleavage at the tripeptide sequence, Arg-Lys-Arg, to yield a disulfide linked dimer. Together with the cofactor Factor V A and Ca2+ on the surface of platelets or endothelial cells, Factor X A coordinates as part of the prothrombinase complex, which mediates proteolysis of Prothrombin into active Thrombin. Mutations at the Factor X locus resulting in Factor X deficiencies can contribute to hemorrhagic diathesis.

APPLICATION DILUTION

IF(IHC-P)(1:50-200)












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