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Katalogové číslo: (APOSOR0545-100G)
Dodavatel: Apollo Scientific
Popis: Hypoxanthine 98%
Měrná jednotka: 1 * 100 g


Dodavatel: Thermo Scientific
Popis: Hypoxanthine 99.5%

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Dodavatel: Thermo Scientific
Popis: Hypoxanthine ≥99%
Katalogové číslo: (BOSSBS-9026R-CY7)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


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

Dodavatel: US Biological
Popis: Anti-Hypoxanthine Phosphoribosyltransferase 1 Mouse Monoclonal Antibody [clone: 12L7]

Katalogové číslo: (BOSSBS-8552R-HRP)
Dodavatel: Bioss
Popis: 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.
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-9026R-A647)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-9026R-A680)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-9026R-A750)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-11739R)
Dodavatel: Bioss
Popis: 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.
Měrná jednotka: 1 * 100 µl


Katalogové číslo: (BOSSBS-9026R-CY3)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


Dodavatel: Merck
Popis: Hypoxanthine, Sigma-Aldrich®

Katalogové číslo: (HYCLSH30025.01)
Dodavatel: HyClone products (Cytiva)
Popis: 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.
Měrná jednotka: 1 * 500 mL


Katalogové číslo: (BOSSBS-9026R-A488)
Dodavatel: Bioss
Popis: 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].
Měrná jednotka: 1 * 100 µl


Dodavatel: MP Biomedicals
Popis: Hypoxanthine is a nutrient additive for a variety of cell culture applications involving bacterial, parasite (Plasmodium falciparum) and animal cells. Hypoxanthine is a component of selection media used in hybridoma technologies.

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