54250 Results for: "Intrinsic+factor"

Supplier: MP Biomedicals

Preparation Method: MP Intrinsic Factor is produced from the pylorus mucous membrane of the pig, of which only a small part is used. Only the part which, according to histological examinations has proved to have a high content of Intrinsic Factor, is used.
Applications: Intrinsic Factor is used in the treatment not only of classical pernicious anaemia, but also in the treatment of other macrocytic anaemias, where it replaces the Intrinsic Factor which may be lacking in the patient's own gastric juice. In this way Intrinsic Factor is recommended against anaemias that appear 6 to 12 months after serious gastric operations, and against anaemias that are secondary effects of the treatment with certain medicines, e.g. against epilepsy. However, the dietetic use in multi-vitamin preparations is of the greatest importance. In older people there has been observed a degeneration of the gastric mucous membrane, whose secretion of Intrinsic Factor is insufficient to ensure the resorption of the necessary quantity of B-12 from their diet. In order to delay this development it is useful to prescribe a small quantity of Intrinsic Factor with B-12 and other vitamins to these patients.
Product Description: Intrinsic factor is a glucoprotein extracted from the pylorus part of the gastric mucous membrane. Its presence is considered necessary for the absorption of Vitamin B-12.
Unit Definition: The activity is normally indicated in Coli units, the number of which are proportional to the binding power of the substance to Vitamin B-12.

Application Areas: Absorption of vitamin B12
Product Type: Proteins, Enzymes & Peptides
Presentation: Tan Powder
Foreign activity: Salmonella=Negative, E. coli=Negative
NOTES: Standard Plate Count <1000/g
Solubility: Slightly soluble in toluene; practically insoluble in water.
Storage & Handling: -20°C

Supplier: Biorbyt

Pig Intrinsic Factor

Supplier: US Biological

Anti-Intrinsic Factor Rabbit Polyclonal Antibody

Supplier: Abcam

Rabbit polyclonal to Intrinsic Factor.

Supplier: ANTIBODIES.COM

Human Intrinsic Factor ELISA kit is a sandwich Enzyme-Linked Immunosorbent Assay (sELISA) designed for the in vitro quantitative determination of human Intrinsic Factor in serum, plasma, tissue homogenates, and other biological fluids.

Supplier: Abcam

Rabbit polyclonal to Intrinsic Factor.

Supplier: ANTIBODIES.COM

Rabbit polyclonal antibody to Intrinsic Factor for WB and ICC/IF with samples derived from human and mouse.

Supplier: Biorbyt

Human Intrinsic Factor (from Insect cells (Sf9))

Supplier: Abcam

Rabbit monoclonal [EPR13488(B)] to Intrinsic Factor.

Supplier: Abcam

Rabbit monoclonal [EPR13488(B)] to Intrinsic Factor - BSA and Azide free.

Supplier: Abcam

Rabbit polyclonal to Factor B.

Supplier: Abcam

Rabbit polyclonal to Factor X.

Supplier: US Biological

Anti-Factor H Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Factor B Sheep Polyclonal Antibody

Supplier: Apollo Scientific

Anti-Factor-IX Mouse Antibody

Supplier: US Biological

Anti-Factor H Sheep Polyclonal Antibody

Supplier: Bioss

Anti-Factor B Rabbit Polyclonal Antibody

Supplier: US Biological

Anti-Factor I Sheep Polyclonal Antibody

Supplier: Abcam

Anti-Factor H Goat Polyclonal Antibody

Supplier: US Biological

Anti-Factor H Goat Polyclonal Antibody

Supplier: US Biological

Anti-Factor B Goat Polyclonal Antibody

Supplier: Abcam

Anti-Factor X Rabbit Polyclonal Antibody

Supplier: Biorbyt

Anti-Platelet Factor 4Platelet Factor 4 Rabbit Polyclonal Antibody

Supplier: ENZO LIFE SCIENCES

Factor H is a regulatory factor of the alternative pathway of complement activation. Factor H is a glycoprotein consisting of a single polypeptide chain with a molecular mass of 150kDa.

Supplier: Abcam

Rabbit polyclonal to Factor Xa.

Supplier: Abcam

Sheep polyclonal to Factor XIII.

Supplier: Abcam

Rabbit polyclonal to Factor XIIIa.

Supplier: Abcam

Biotin Rabbit polyclonal to Factor V.

Supplier: Bioss

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.

Supplier: ProSci Inc.

Coagulation factor IX（F9), is a member of the peptidase S1 family. It contains two EGF-like domains, a Gla domain and a peptidase S1 domain. It is primarily expressed in the liver and secreted in plasma. Factor IX is a vitamin K-dependent plasma protein that participates in the intrinsic pathway of blood coagulation by converting factor X to its active form in the presence of Ca2+ ions, phospholipids, and factor VIIIa. Mutations in position 43 and 46 prevents cleavage of the propeptide, mutation in position 93 probably fails to bind to cell membranes, mutation in position 191 or in position 226 prevent cleavage of the activation peptide. Mutations of human F9 can result in thrombophilia and recessive X-linked hemophilia B (HEMB). An X-linked blood coagulation disorder characterized by a permanent tendency to hemorrhage, due to factor IX deficiency. It is phenotypically similar to hemophilia A, but patients present with fewer symptoms. Many patients are asymptomatic until the hemostatic system is stressed by surgery or trauma.