You Searched For: Mesoporphyrin+IX+dihydrochloride

Catalog Number: (MLDV5085430)

Supplier: Molecular Devices

Description: Photodocumentation System, IX-C HT.ai GEN2 Transmitted light/environmental control option, 240 V

UOM: 1 * 1 items

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Catalog Number: (BOSSBS-12868R-A680)

Supplier: Bioss

Description: In human liver cytosolic fractions, four forms of biliverdin reductase have been identified, including two biliverdin-IX Beta reductases and two biliverdin-IX Alpha reductases, designated isozymes I and II and isozymes III and IV, respectively. Biliverdin reductase A (BLVRA), also designated biliverdin-IX Alpha-reductase, belongs to the GFO/iIDH/MocA family and the biliverdin reductase subfamily. The gene that encodes this cytoplasmic protein maps to chromosome 7p14-cen. BLVRA reduces biliverdin IX (the methene bridge of the open tetrapyrrole) to bilirubin with the concomitant oxidation of an NADH or NADPH cofactor (bilirubin + NADP+ = biliverdin + NADPH). BLVRA is expressed primarily in liver.

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-9500R-CY7)

Supplier: Bioss

Description: 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 (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-9500R-A350)

Supplier: Bioss

Description: 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 (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).

UOM: 1 * 100 µl

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Catalog Number: (BOSSBS-9500R-A555)

Supplier: Bioss

Description: 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 (1-3). Coagulation factor IX (plasma thromboplastic component, F9, F.IX, HEMB) is a vitamin K-dependent, single chain serine protease that is synthesized in the liver and circulates as an inactive precursor (3,4). Factor XIa mediated proteolytic cleavage of factor IX generates factor IXa, an active serine protease composed of a 145 amino acid light chain and a 236 amino acid catalytic heavy chain, linked through disulfide bonds (5). Genetic alterations at the Factor IX locus such as point mutations, insertions and deletions, can lead to hemophilia B, also known as Christmas disease (6).

UOM: 1 * 100 µl

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Catalog Number: (172-0033)

Supplier: Merck

Description: Pure and Ultra Pure Water System, Water sensor, safety accessory that detects a water leak, for use with Milli-Q® IQ/IX/EQ/SQ series

UOM: 1 * 1 items

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Supplier: Merck

Description: Pure and Ultra Pure Water System, Milli-Q®, Country box Milli-Q® IX 7003/5/10/15, EU

Catalog Number: (PRSI92-398)

Supplier: ProSci Inc.

Description: 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.

UOM: 1 * 0,05 mg

New Product Sale

Supplier: Thermo Fisher Scientific

Description: Zinc protoporphyrin ≥96%

MSDS Certificates

Catalog Number: (QTUM000IX)

Supplier: Merck

Description: Pure and Ultra Pure Water System, Quantum IX ultrapurification cartridge with Millipak final filter

UOM: 1 * 1 items

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Supplier: Novus Biologicals

Description: The Carbonic Anhydrase IX / CA9 Antibody (2D3) from Novus Biologicals is a mouse monoclonal antibody to Carbonic Anhydrase IX / CA9. This antibody reacts with human. The Carbonic Anhydrase IX / CA9 Antibody (2D3) has been validated for the following applications: Western Blot, Flow Cytometry, ELISA, Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin, Flow (Intracellular), CyTOF-ready.

Supplier: Apollo Scientific

Description: MAPK/ERK Signalling Pathway

Catalog Number: (BOSSBS-12868R-FITC)

Supplier: Bioss

Description: In human liver cytosolic fractions, four forms of biliverdin reductase have been identified, including two biliverdin-IX Beta reductases and two biliverdin-IX Alpha reductases, designated isozymes I and II and isozymes III and IV, respectively. Biliverdin reductase A (BLVRA), also designated biliverdin-IX Alpha-reductase, belongs to the GFO/iIDH/MocA family and the biliverdin reductase subfamily. The gene that encodes this cytoplasmic protein maps to chromosome 7p14-cen. BLVRA reduces biliverdin IX ?(the ?methene bridge of the open tetrapyrrole) to bilirubin with the concomitant oxidation of an NADH or NADPH cofactor (bilirubin + NADP+ = biliverdin + NADPH). BLVRA is expressed primarily in liver.

UOM: 1 * 100 µl

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Catalog Number: (NOVUNB100-417B)

Supplier: Novus Biologicals

Description: The Carbonic Anhydrase IX / CA9 Antibody [Biotin] from Novus Biologicals is a rabbit polyclonal antibody to Carbonic Anhydrase IX/CA9. This antibody reacts with human, mouse, rat, canine, plant. The Carbonic Anhydrase IX / CA9 Antibody [Biotin] has been validated for the following applications: Western Blot, ELISA, Immunohistochemistry, Immunocytochemistry/Immunofluorescence, Immunohistochemistry-Paraffin, Immunohistochemistry-Frozen.

UOM: 1 * 0,1 mL

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Catalog Number: (QTUMMPKIX)

Supplier: Merck

Description: Pure and ultra pure water system, Cartridge Quantum IX with Millipak-40 filter

UOM: 1 * 1 items

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Catalog Number: (BOSSBS-12868R-A750)

Supplier: Bioss

Description: In human liver cytosolic fractions, four forms of biliverdin reductase have been identified, including two biliverdin-IX Beta reductases and two biliverdin-IX Alpha reductases, designated isozymes I and II and isozymes III and IV, respectively. Biliverdin reductase A (BLVRA), also designated biliverdin-IX Alpha-reductase, belongs to the GFO/iIDH/MocA family and the biliverdin reductase subfamily. The gene that encodes this cytoplasmic protein maps to chromosome 7p14-cen. BLVRA reduces biliverdin IX (the methene bridge of the open tetrapyrrole) to bilirubin with the concomitant oxidation of an NADH or NADPH cofactor (bilirubin + NADP+ = biliverdin + NADPH). BLVRA is expressed primarily in liver.

UOM: 1 * 100 µl

Sale