Hai cercato: Magnesium+tetraborate

Fornitore: Honeywell Chemicals

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

MSDS

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: Thermo Fisher Scientific

Descrizione: Standard di magnesio, 1000 mg/L, Specpure®, Magnesio, Matrice: 5% HNO₃, Applicazione: Standard per ICP

MSDS Certificati

Codice catalogo: (428892-100ML)

Fornitore: Honeywell Chemicals

Codice articolo fornitore: 428892-100ML

Codice articolo locale: HONC428892-100ML

Descrizione: The acids, bases, and salts in the TraceSELECT series have been developed for sample preparation and analysis in the ppb (µg/kg) trace range.

UOM: 1 * 100 mL

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

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

Fornitore: MERCK PRODUCTION CHEMICALS

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

MSDS

Codice catalogo: (BOSSBS-9433R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-9433R-CY7

Codice articolo locale: BOSSBS-9433R-CY7

Descrizione: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9433R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-9433R-CY5

Codice articolo locale: BOSSBS-9433R-CY5

Descrizione: FIGNL1 is a 674 amino acid protein belonging to the AAA ATPase family. FIGNL1 exists as a hexamer that undergoes alternative splicing to produce two isoforms. FIGNL1 utilizes magnesium as a cofactor and is phosphorylated upon DNA damage, probably by ATM or ATR. FIGNL1 is suggested to regulate osteoblast proliferation and differentiation. FIGNL1 is encoded by a gene located on human chromosome 7, which consists about 158 milllion bases, encodes over 1000 genes and makes up about 5% of the human genome. Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9734R-CY3)

Fornitore: Bioss

Codice articolo fornitore: BS-9734R-CY3

Codice articolo locale: BOSSBS-9734R-CY3

Descrizione: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. TSSK 6 (testis-specific serine kinase 6), also known as SSTK, TSSK4, FKSG82 or CT72, is a 273 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase family. Highly expressed in testis with lower expression in ovary, colon, thymus, small intestine and spleen, TSSK 6 catalyzes the ATP-dependent phosphorylation of proteins involved in sperm production and chromatin remodeling. TSSK 6 uses magnesium as a cofactor and is thought to be required for proper sperm development and function, as well as DNA condensation events. Defects in the gene encoding TSSK 6 are associated with male infertility characterized by low sperm count and decreased sperm motility.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9734R)

Fornitore: Bioss

Codice articolo fornitore: BS-9734R

Codice articolo locale: BOSSBS-9734R

Descrizione: The phosphorylation and dephosphorylation of proteins on serine and threonine residues is an essential means of regulating a broad range of cellular functions in eukaryotes, including cell division, homeostasis and apoptosis. A group of proteins that are intimately involved in this process are the serine/threonine (Ser/Thr) protein kinases. TSSK 6 (testis-specific serine kinase 6), also known as SSTK, TSSK4, FKSG82 or CT72, is a 273 amino acid protein that contains one protein kinase domain and belongs to the Ser/Thr protein kinase family. Highly expressed in testis with lower expression in ovary, colon, thymus, small intestine and spleen, TSSK 6 catalyzes the ATP-dependent phosphorylation of proteins involved in sperm production and chromatin remodeling. TSSK 6 uses magnesium as a cofactor and is thought to be required for proper sperm development and function, as well as DNA condensation events. Defects in the gene encoding TSSK 6 are associated with male infertility characterized by low sperm count and decreased sperm motility.

UOM: 1 * 100 µl

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

Codice catalogo: (BOSSBS-8228R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-8228R-HRP

Codice articolo locale: BOSSBS-8228R-HRP

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-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-8228R-A488

Codice articolo locale: BOSSBS-8228R-A488

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: (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