Sie suchten nach: Hypoxanthin

Artikel-Nr: (APOSOR0545-100G)

Lieferant: Apollo Scientific

Beschreibung: Hypoxanthin 98%

VE: 1 * 100 g

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Lieferant: Thermo Scientific

Beschreibung: Hypoxanthin 99.5%

Sicherheitsdatenblätter

Lieferant: Thermo Scientific

Beschreibung: Hypoxanthin ≥99%

Sicherheitsdatenblätter Zertifikate

Artikel-Nr: (BOSSBS-9026R-CY7)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

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Lieferant: Apollo Scientific

Beschreibung: 6-Mercaptopurine is an antineoplastic agent which acts asan antimetabolite. It is an analogue of the natural purines hypoxanthine and adenine.

Lieferant: US Biological

Beschreibung: Anti-Hypoxanthine Phosphoribosyltransferase 1 Mouse Monoclonal Antibody [clone: 12L7]

Artikel-Nr: (BOSSBS-8552R-HRP)

Lieferant: Bioss

Beschreibung: Key enzyme in purine degradation. Catalyzes the oxidation of hypoxanthine to xanthine. Catalyzes the oxidation of xanthine to uric acid. Contributes to the generation of reactive oxygen species. Has also low oxidase activity towards aldehydes (in vitro).Involvement in disease;Defects in XDH are the cause of xanthinuria type 1 (XU1) . Xanthinuria is characterized by excretion of very large amounts of xanthine in the urine and a tendency to form xanthine stones. Uric acid is strikingly diminished in serum and urine. XU1 is due to isolated xanthine dehydrogenase. XU1 patients can metabolize allopurinol.

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-9026R-A647)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-9026R-A750)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

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Artikel-Nr: (BOSSBS-9026R-A680)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

Sale!

Artikel-Nr: (BOSSBS-9026R-CY3)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

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Artikel-Nr: (4010CBC-25GM)

Lieferant: Merck Millipore (Calbiochem‎)

Beschreibung: Hypoxanthin, Millipore®

VE: 1 * 25 g

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Artikel-Nr: (BOSSBS-11739R)

Lieferant: Bioss

Beschreibung: Purine nucleoside phosphorylase (PNP), also designated inosine phosphorylase, forms a homotrimer. It belongs to the PNP/MTAP phosphorylase family of proteins. Human PNP catalyzes the reversible phosphorolysis of ribonucleosides and 2’-deoxyribonucleosides with specificity for guanine, hypoxanthine, and their analogs. PNP deficiency is a rare autosomal recessive genetic disease associated with a severe defect in T-lymphocyte function and neurologic disorder in children, comprising four percent of combined immunodeficiency cases. Children with PNP deficiency are highly prone to infections, autoimmune disorders, neurological impairment, and cancer.

VE: 1 * 100 µl

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Lieferant: Merck

Beschreibung: Hypoxanthin, Sigma-Aldrich®

Artikel-Nr: (HYCLSH30025.01)

Lieferant: HyClone products (Cytiva)

Beschreibung: Ham's F-10 was designed for use with Chinese Hamster Ovary (CHO) cells, and has been shown to support the growth of human diploid cells, white blood cells, and primary explants from rat, rabbit, or chicken tissues. This classical media can be used for serum-free growth of some cell lines including CHO cells. Serum supplementation may or may not be necessary depending on the type of cell being cultured. Ham's F-10 contains a wide variety of components, including zinc, hypoxanthine, and thymidine and is buffered with sodium bicarbonate.

VE: 1 * 500 mL

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Artikel-Nr: (BOSSBS-9026R-A488)

Lieferant: Bioss

Beschreibung: The protein encoded by this gene is a transferase, which catalyzes conversion of hypoxanthine to inosine monophosphate and guanine to guanosine monophosphate via transfer of the 5-phosphoribosyl group from 5-phosphoribosyl 1-pyrophosphate. This enzyme plays a central role in the generation of purine nucleotides through the purine salvage pathway. Mutations in this gene result in Lesch-Nyhan syndrome or gout.[provided by RefSeq, Jun 2009].

VE: 1 * 100 µl

Sale!