Hai cercato: Magnesium+tetraborate

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

MSDS

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 Promo

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

Promo

Fornitore: MERCK PRODUCTION CHEMICALS

Descrizione: Magnesio ossido leggero Ph. Eur., BP, E530, extra puro, SAFC®

MSDS Certificati

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

Promo

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

Promo

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

Promo

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

Promo

Fornitore: Honeywell Chemicals

Descrizione: Magnesio solfato idrato, essicato 99.0-101.0% (dried basis), Puriss., meets analytical specification of DAC, Fluka™

MSDS

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

Promo

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™

MSDS Certificati

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

Promo

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

MSDS Certificati Promo

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

Promo

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

Promo