Hai cercato: Magnesium+tetraborate

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: (BOSSBS-12039R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-12039R-A350

Codice articolo locale: BOSSBS-12039R-A350

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: (BOSSBS-12039R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-12039R-FITC

Codice articolo locale: BOSSBS-12039R-FITC

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: (PERCN2025330)

Fornitore: PerkinElmer

Codice articolo fornitore: N2025330

Codice articolo locale: PERCN2025330

Descrizione: Lampada a catodo cavo, Atomax™, Per: Non Perkin-Elmer instruments, Magnesio

UOM: 1 * 1 pezzi

Promo

Fornitore: LGC Standards PROMOCHEM

Descrizione: The solutions are intended for use as a certified reference material or calibration standard for inductively coupled plasma optical emission spectroscopy (ICP-OES), inductively coupled plasma mass spectrometry (ICP-MS), flame or furnace atomic absorption spectroscopy (AA or GFAA), x-ray fluorescence spectroscopy (XRF), and other techniques for elemental analysis.

Fornitore: Hach

Descrizione: Reagents for photometric analysis either in field conditions or in the laboratory.

Certificati

Codice catalogo: (ICNA092820549)

Fornitore: MP Biomedicals

Codice articolo fornitore: 092820549

Codice articolo locale: ICNA092820549

Descrizione: EDTA disodium salt, (2%) solution, in phosphate buffered saline without calcium and magnesium. Used as a gentle non-enzymatic cell dissociation reagent.

UOM: 1 * 100 mL

Promo

Codice catalogo: (PRSI29-943)

Fornitore: ProSci Inc.

Codice articolo fornitore: 29-943

Codice articolo locale: PRSI29-943

Descrizione: SLC41A2 acts as a plasma-membrane magnesium transporter.

UOM: 1 * 100 µG

Promo

Codice catalogo: (HACH2062501)

Fornitore: Hach

Codice articolo fornitore: 2062501

Codice articolo locale: HACH2062501

Descrizione: Digital titration provides a more precise and accurate method than the drop test method.

UOM: 1 * 1 pezzi

Promo

Codice catalogo: (PRSI30-142)

Fornitore: ProSci Inc.

Codice articolo fornitore: 30-142

Codice articolo locale: PRSI30-142

Descrizione: MTHFD2 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 * 100 µG

Promo

Codice catalogo: (15-015-CV)

Fornitore: Corning

Codice articolo fornitore: 15-015-CV

Codice articolo locale: MDTC15-015-CV

Descrizione: A complete range of classical cell culture media are available.

UOM: 1 * 6 pezzi

Certificati Promo

Codice catalogo: (AATB20404)

Fornitore: AAT BIOQUEST

Codice articolo fornitore: 20404

Codice articolo locale: AATB20404

Descrizione: A vast majority of the existing magnesium ion indicators are based on tricarboxylate APTRA chelator derived from the popular tetracarboxylate BAPTA calcium ion chelator.

UOM: 1 * 500 µG

Promo

Fornitore: Corning

Descrizione: 0,05% Trypsin/0,53 mM EDTA in HBSS (Hank’s Balanced Salt Solution) with sodium bicarbonate, without calcium and magnesium.

Certificati

Codice catalogo: (USBIA1372-25A-100L)

Fornitore: US Biological

Codice articolo fornitore: A1372-25A-100L

Codice articolo locale: USBIA1372-25A-100L

Descrizione: Ames' medium was formulated to support retinal tissue in relatively short-term culture.

UOM: 1 * 1 pezzi

Promo