Hai cercato: Magnesium+tetraborate

Codice catalogo: (PRSI56-175)

Fornitore: ProSci Inc.

Codice articolo fornitore: 56-175

Codice articolo locale: PRSI56-175

Descrizione: PDPR decreases the sensitivity of PDP1 to magnesium ions, and this inhibition is reversed by the polyamine spermine (By similarity).

UOM: 1 * 400 µl

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Codice catalogo: (HACH1430598)

Fornitore: Hach

Codice articolo fornitore: 1430598

Codice articolo locale: HACH1430598

Descrizione: Buffered dilution water required for testing recreational, drinking and wastewater.

UOM: 1 * 25 pezzi

Promo

Codice catalogo: (BOSSBS-8228R-CY5.5)

Fornitore: Bioss

Codice articolo fornitore: BS-8228R-CY5.5

Codice articolo locale: BOSSBS-8228R-CY5.5

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-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-12039R-CY7

Codice articolo locale: BOSSBS-12039R-CY7

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-12001R)

Fornitore: Bioss

Codice articolo fornitore: BS-12001R

Codice articolo locale: BOSSBS-12001R

Descrizione: MAP (mitogen-activated protein) kinases play a significant role in many biological processes, including cell adhesion and spreading, cell differentiation and apoptosis. p38 alpha, p38 beta and p38 gamma, also known as MAPK14, MAPK11 and MAPK12, respectively, each contain one protein kinase domain and belong to the MAP kinase family. Expressed in different areas throughout the body with common expression patterns in heart, p38 proteins use magnesium as a cofactor to catalyze the ATP-dependent phosphorylation of target proteins. Via their catalytic activity, p38 alpha, p38 beta and p38 gamma are involved in a variety of events throughout the cell, including signal transduction pathways, cytokine production and cell proliferation and differentiation. The p38 proteins are subject to phosphoryation on Thr and Tyr residues, an event which is thought to activate the phosphorylated protein.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-12039R-HRP)

Fornitore: Bioss

Codice articolo fornitore: BS-12039R-HRP

Codice articolo locale: BOSSBS-12039R-HRP

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-9433R)

Fornitore: Bioss

Codice articolo fornitore: BS-9433R

Codice articolo locale: BOSSBS-9433R

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

Fornitore: PerkinElmer

Descrizione: Lampada a catodo cavo, Lumina™, Per: Perkin-Elmer instruments, Elemento singolo, magnesio

Fornitore: Corning

Descrizione: Phosphate buffered saline (PBS) is a buffer solution containing sodium chloride, sodium phosphate, and in some formulations potassium chloride and potassium phosphate

Certificati

Codice catalogo: (AATB21052)

Fornitore: AAT BIOQUEST

Codice articolo fornitore: 21052

Codice articolo locale: AATB21052

Descrizione: Quin-2 binds calcium tightly and resembles calcium chelator EGTA in ability to bind calcium much more tightly than magnesium.

UOM: 1 * 5 mg

Promo

Codice catalogo: (635-0259)

Fornitore: Atago

Codice articolo fornitore: 4455

Codice articolo locale: ATAG4455

Descrizione: The PAL series for pharmaceutical ingredients (reagents) are pocket instruments delivering rapid results.

UOM: 1 * 1 pezzi

Promo

Codice catalogo: (ICNA091688449)

Fornitore: MP Biomedicals

Codice articolo fornitore: 091688449

Codice articolo locale: ICNA091688449

Descrizione: HEPES (N-2-hydroxyethylpiperazine-N-2-ethane sulfonic acid) is a general purpose zwitterionic organic chemical buffering agent which does not bind magnesium, calcium, manganese(II) or copper (II) ions.

UOM: 1 * 100 mL

Promo

Fornitore: MP Biomedicals

Descrizione: Phosphate buffered salts, Dulbecco's formula (DPBS) is a balanced salt solution (BSS) used for the handling and culturing of mammalian cells. DPBS is used to to irrigate, wash, and dilute mammalian cells.

MSDS

Codice catalogo: (J67795.AP)

Fornitore: Thermo Fisher Scientific

Codice articolo fornitore: J67795.AP

Codice articolo locale: ALFAJ67795.AP

Descrizione: Contains 120 mM sodium chloride, 5 mM potassium chloride, 2 mM calcium chloride, 1 mM magnesium chloride, 25 mM sodium bicarbonate, 5,5 mM HEPES, and 1 mM D-glucose

UOM: 1 * 500 mL

MSDS Certificati Promo

Codice catalogo: (BOSSBS-9433R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-9433R-A680

Codice articolo locale: BOSSBS-9433R-A680

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 million 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 characterised 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 leukaemia and myelodysplasia.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-9734R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-9734R-A680

Codice articolo locale: BOSSBS-9734R-A680

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 catalyses 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 characterised by low sperm count and decreased sperm motility.

UOM: 1 * 100 µl

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