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Hai cercato: Magnesium+tetraborate


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Codice catalogo: (BOSSBS-8228R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-8228R-A647
Codice articolo locale: BOSSBS-8228R-A647
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-CY3)
Fornitore: Bioss
Codice articolo fornitore: BS-12039R-CY3
Codice articolo locale: BOSSBS-12039R-CY3
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: (BOSSBS-12039R-A555)
Fornitore: Bioss
Codice articolo fornitore: BS-12039R-A555
Codice articolo locale: BOSSBS-12039R-A555
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: (BOSSBS-12039R-A647)
Fornitore: Bioss
Codice articolo fornitore: BS-12039R-A647
Codice articolo locale: BOSSBS-12039R-A647
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: (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

New Product


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

Codice catalogo: (18654-25KG)
Fornitore: Honeywell Chemicals
Codice articolo fornitore: 18654-25KG
Codice articolo locale: HONC18654-25KG
Descrizione: Talco, in polvere, meets analytical specification of BP, Ph. Eur., Fluka™
UOM: 1 * 25 kg


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


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


Codice catalogo: (BOSSBS-9433R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-9433R-FITC
Codice articolo locale: BOSSBS-9433R-FITC
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


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.
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

Codice catalogo: (705-3048)
Fornitore: Hach
Codice articolo fornitore: LCK326
Codice articolo locale: HACHLCK326
Descrizione: Reagenti predosati per la massima sicurezza. Facile da utilizzare, per valutazione fotometrica, in una scatola completa di tutti i reagenti necessari. A basso impatto ambientale grazie alla quantità ridotta di prodotti chimici.
UOM: 1 * 25 Tests


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


Fornitore: Corning
Descrizione: Dulbecco's Phosphate Buffered Saline (DPBS) is a buffer solution which can be used to maintain cell culture media in the physiological pH range of 7,0 to 7,6
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