Votre recherche pour: NADPH-Na4

Numéro de catalogue: (BOSSBS-3891R-A750)

Fournisseur: Bioss

Description: This gene encodes neutrophil cytosolic factor 2, the67-kilodalton cytosolic subunit of the multi-protein NADPH oxidase complex found in neutrophils. This oxidase produces a burst of superoxide which is delivered to the lumen of the neutrophil phagosome. Mutations in this gene, as well as in other NADPH oxidase subunits, can result in chronic granulomatous disease, a disease that causes recurrent infections by catalase-positive organisms. Alternative splicing results in multiple transcript variants encoding different isoforms.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-1498R-CY5.5)

Fournisseur: Bioss

Description: Fatty acid synthetase catalyses the formation of long-chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities and an acyl carrier protein.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-10156R-A488)

Fournisseur: Bioss

Description: Calcium-dependent NADPH oxidase that generates superoxide. Also functions as a calcium-dependent proton channel and may regulate redox-dependent processes in lymphocytes and spermatozoa. May play a role in cell growth and apoptosis.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13462R-A750)

Fournisseur: Bioss

Description: This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. The protein also functions in the re-utilization of free intracellular bases and purine nucleosides.[provided by RefSeq, Oct 2009].

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13462R-A350)

Fournisseur: Bioss

Description: This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. The protein also functions in the re-utilization of free intracellular bases and purine nucleosides.[provided by RefSeq, Oct 2009].

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-3886R-CY3)

Fournisseur: Bioss

Description: NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production).

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-1498R-A647)

Fournisseur: Bioss

Description: Fatty acid synthetase catalyses the formation of long-chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities and an acyl carrier protein.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-1498R-A750)

Fournisseur: Bioss

Description: Fatty acid synthetase catalyses the formation of long-chain fatty acids from acetyl-CoA, malonyl-CoA and NADPH. This multifunctional protein has 7 catalytic activities and an acyl carrier protein.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13462R-HRP)

Fournisseur: Bioss

Description: This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. The protein also functions in the re-utilization of free intracellular bases and purine nucleosides.[provided by RefSeq, Oct 2009].

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-12868R-HRP)

Fournisseur: 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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Numéro de catalogue: (BOSSBS-12868R-CY7)

Fournisseur: 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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Numéro de catalogue: (BOSSBS-3856R-A647)

Fournisseur: Bioss

Description: Capable of catalyzing the interconversion of testosterone and androstenedione, as well as estradiol and estrone. Also has 20-alpha-HSD activity. Uses NADH while EDH17B3 uses NADPH.

UOM: 1 * 100 µl

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Numéro de catalogue: (BOSSBS-13462R)

Fournisseur: Bioss

Description: This gene encodes an enzyme that catalyzes the irreversible and NADPH-dependent reductive deamination of GMP to IMP. The protein also functions in the re-utilization of free intracellular bases and purine nucleosides.[provided by RefSeq, Oct 2009].

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-3891R-CY3)

Fournisseur: Bioss

Description: This gene encodes neutrophil cytosolic factor 2, the67-kilodalton cytosolic subunit of the multi-protein NADPH oxidase complex found in neutrophils. This oxidase produces a burst of superoxide which is delivered to the lumen of the neutrophil phagosome. Mutations in this gene, as well as in other NADPH oxidase subunits, can result in chronic granulomatous disease, a disease that causes recurrent infections by catalase-positive organisms. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq].

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-3891R-A647)

Fournisseur: Bioss

Description: This gene encodes neutrophil cytosolic factor 2, the67-kilodalton cytosolic subunit of the multi-protein NADPH oxidase complex found in neutrophils. This oxidase produces a burst of superoxide which is delivered to the lumen of the neutrophil phagosome. Mutations in this gene, as well as in other NADPH oxidase subunits, can result in chronic granulomatous disease, a disease that causes recurrent infections by catalase-positive organisms. Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq].

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-3886R-A555)

Fournisseur: Bioss

Description: NCF2, NCF1, and a membrane bound cytochrome b558 are required for activation of the latent NADPH oxidase (necessary for superoxide production).

UOM: 1 * 100 µl

Promotion