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Hai cercato: Magnesium+tetraborate


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Fornitore: CPACHEM
Descrizione: Standard di magnesio, 1000 mg/L, Magnesio, Matrice: H₂O, Applicazione: Standard di cromatografia ionica

Fornitore: PerkinElmer
Descrizione: Standard di magnesio, 1000 mg/L, Magnesio, Matrice: 2% HNO₃, Applicazione: Standard per ICP
Codice catalogo: (25-051-CI)
Fornitore: Corning
Codice articolo fornitore: 25-051-CI
Codice articolo locale: MDTC25-051-CI
Descrizione: 0,05% Trypsin/0,53 mM EDTA in HBSS (Hank’s Balanced Salt Solution) with sodium bicarbonate, without calcium and magnesium.
UOM: 1 * 6 pezzi

Certificati


Codice catalogo: (459-2912)
Fornitore: CERAM TEC
Codice articolo fornitore: 4.014347.00.00
Codice articolo locale: CERA4.014347.00.00
Descrizione: For flame reaction
UOM: 1 * 100 pezzi


Fornitore: MERCK PRODUCTION CHEMICALS
Descrizione: Magnesio ossido leggero Ph. Eur., BP, E530, extra puro, SAFC®
Codice catalogo: (BOSSBS-8228R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-8228R-CY7
Codice articolo locale: BOSSBS-8228R-CY7
Descrizione: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-12039R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-12039R-CY5
Codice articolo locale: BOSSBS-12039R-CY5
Descrizione: GDE1 is a 331 amino acid multi-pass membrane protein that localizes to both the membrane and the cytoplasm and contains one GDPD domain. Expressed in a wide variety of tissues, GDE1 uses magnesium as a cofactor to catalyze the conversion of 1-(sn-glycero-3-phospho)-1D-myo-inositol to myo-inositol and sn-glycerol 3-phosphate, an event that is modulated by G protein signaling pathways and provides a link between phosphoinositide metabolism and G protein signal transduction. The gene encoding GDE1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3% of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.
UOM: 1 * 100 µl


Codice catalogo: (PRSI26-095)
Fornitore: ProSci Inc.
Codice articolo fornitore: 26-095
Codice articolo locale: PRSI26-095
Descrizione: This protein is a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. This gene encodes a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. Alternative splicing results in multiple transcripts encoding different isoforms. This gene has a pseudogene on chromosome 7.
UOM: 1 * 50 µG


Codice catalogo: (PERCN9303743)
Fornitore: PerkinElmer
Codice articolo fornitore: N9303743
Codice articolo locale: PERCN9303743
Descrizione: Single element standard is supplied with a comprehensive Certificate of Analysis that documents the quality and reliability.
UOM: 1 * 1 pezzi


Fornitore: Honeywell Chemicals
Descrizione: Magnesio solfato idrato, essicato 99.0-101.0% (dried basis), Puriss., meets analytical specification of DAC, Fluka™
Codice catalogo: (BOSSBS-8228R)
Fornitore: Bioss
Codice articolo fornitore: BS-8228R
Codice articolo locale: BOSSBS-8228R
Descrizione: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
UOM: 1 * 100 µl


Fornitore: Honeywell Chemicals
Descrizione: Magnesio ossido leggero, essicato 98.0-100.5% (dried basis), Puriss., meets analytical specification of BP, Ph. Eur., USP, FCC, E530, Fluka™
Codice catalogo: (AATB20406)
Fornitore: AAT BIOQUEST
Codice articolo fornitore: 20406
Codice articolo locale: AATB20406
Descrizione: Intracellular magnesium is important for mediating enzymatic reactions, DNA synthesis, hormone secretion, and muscle contraction.
UOM: 1 * 500 µG


Codice catalogo: (25-053-CI)
Fornitore: Corning
Codice articolo fornitore: 25-053-CI
Codice articolo locale: MDTC25-053-CI
Descrizione: 0,05% Trypsin/0,53 mM EDTA in HBSS (Hank’s Balanced Salt Solution) with sodium bicarbonate, without calcium and magnesium.
UOM: 1 * 6 pezzi

Codice catalogo: (BOSSBS-8228R-CY5)
Fornitore: Bioss
Codice articolo fornitore: BS-8228R-CY5
Codice articolo locale: BOSSBS-8228R-CY5
Descrizione: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilize calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstré°‰ syndrome, is also associated with mutations to chromosome 2.
UOM: 1 * 100 µl


Codice catalogo: (BOSSBS-8228R-A680)
Fornitore: Bioss
Codice articolo fornitore: BS-8228R-A680
Codice articolo locale: BOSSBS-8228R-A680
Descrizione: The FAH family contains two highly homologous 314 amino acid proteins, designated FAHD2A (fumarylacetoacetate hydrolase domain-containing protein 2A) and FAHD2B (fumarylacetoacetate hydrolase domain-containing protein 2A). FAHD2A and B utilise calcium and magnesium as cofactors, and may possess hydrolase activity. The genes encoding FAHD2A/B map to human chromosome 2, the second largest human chromosome, which consists of 237 million bases, encodes over 1,400 genes and makes up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is also associated with mutations to chromosome 2.
UOM: 1 * 100 µl


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