Hemophilia
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
Factor VIII is a protein that is typically made in the liver and released into the bloodstream. It is an essential component for normal blood clotting.
Factor VIII is crucial in the intrinsic pathway of the blood coagulation system. It helps in the activation of factor X, which is a key step in the formation of a blood clot. Without factor VIII, this pathway would be impaired, leading to difficulties in clot formation.
To determine the expression pattern of the Factor VIII gene, techniques such as quantitative PCR (qPCR) or RNA sequencing (RNA-seq) can be employed. These methods allow for the quantification of mRNA levels, revealing how and when the Factor VIII gene is expressed in different tissues or under various conditions. Additionally, in situ hybridization can visualize the spatial expression of the gene within tissues. Collectively, these techniques provide insights into the regulation and functional significance of Factor VIII in hemostasis.
the organelle that produces all the proteins in the body is the ribosome, but hemophillia is a genetic condition, so the ribosome is not affected at all but the genetic information that the ribosome needs to produce that specific protein.
Hemophilla is a genetic disorder in which there is absence of clotting factor viii, leading to defective clot formation, petechiae bruising and gum bleeding. Treatment is by injecting factor VIII concentrate
Hemophilia is caused by a deficiency of clotting factor VIII (hemophilia A) or clotting factor IX (hemophilia B).
No Factor VIII is Antihemophilic factor.Thrombocytopenia is a low platlet count Thrombocyte = platlet Penia = poorness
i want know price factor viii
Hemophilia
hemophilia |ˌhēməˈfilēə| ( Brit. haemophilia) noun a medical condition in which the ability of the blood to clot is severely reduced, causing the sufferer to bleed severely from even a slight injury. The condition is typically caused by a hereditary lack of a coagulation factor, most often factor VIII.
Factor VIII is a protein that is typically made in the liver and released into the bloodstream. It is an essential component for normal blood clotting.
Hemophilia A is an X-linked, hereditary bleeding disorder caused by the absence or defect of a blood clotting protein, Factor VIII. As a result, when a person with hemophilia A has a bleeding episode, the bleeding may be prolonged due to the body's inability to form blood clots. Patients who are affected with hemophilia A experience frequent spontaneous bleeding, most commonly into their joints and soft tissues, with bleeding into vital organs that may ... be life-threatening. Bleeding episodes may be painful, and over time, recurrent joint bleeding may result in debilitating destruction of the joints. Currently, patients with hemophilia A are dependent on injections of Factor VIII produced by genetic engineering or purified from human plasma, to help control a bleeding episode. It is estimated that approximately 50,000 individuals worldwide are affected with hemophilia A. Hemophilia A - Clotting Factor VIII Hemophilia B - Clotting Factor IX Hemophilia C - Clotting Factor XI
There are a number of factors involved, Condition is the main factor, how old? Which company made them etc.
Factor VIII is crucial in the intrinsic pathway of the blood coagulation system. It helps in the activation of factor X, which is a key step in the formation of a blood clot. Without factor VIII, this pathway would be impaired, leading to difficulties in clot formation.
factor VIII deficienty
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