Hai cercato: Magnesium+tetraborate

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: (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

Promo

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

Certificati

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

Promo

Fornitore: MP Biomedicals

Descrizione: Nitrilotriacetic acid is an excellent chelating agent which sequester metal ions to form water-soluble complexes; It has many industrial applications. Because of its ability to chelate calcium and magnesium ions.

Fornitore: Thermo Fisher Scientific

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

Certificati

Codice catalogo: (BOSSBS-9433R-A350)

Fornitore: Bioss

Codice articolo fornitore: BS-9433R-A350

Codice articolo locale: BOSSBS-9433R-A350

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-13132R-A680)

Fornitore: Bioss

Codice articolo fornitore: BS-13132R-A680

Codice articolo locale: BOSSBS-13132R-A680

Descrizione: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13132R-CY7)

Fornitore: Bioss

Codice articolo fornitore: BS-13132R-CY7

Codice articolo locale: BOSSBS-13132R-CY7

Descrizione: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13132R-CY5)

Fornitore: Bioss

Codice articolo fornitore: BS-13132R-CY5

Codice articolo locale: BOSSBS-13132R-CY5

Descrizione: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Promo

Codice catalogo: (BOSSBS-13132R-FITC)

Fornitore: Bioss

Codice articolo fornitore: BS-13132R-FITC

Codice articolo locale: BOSSBS-13132R-FITC

Descrizione: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Promo

Codice catalogo: (HACH225100)

Fornitore: Hach

Codice articolo fornitore: 225100

Codice articolo locale: HACH225100

Descrizione: High concentrations of magnesium or sodium sulphate in water act as cathartics. This test kit provides economical determination of sulphate levels using the Extinction/Turbidimetric methods.

UOM: 1 * 1 KIT

Promo

Codice catalogo: (BOSSBS-13132R-A488)

Fornitore: Bioss

Codice articolo fornitore: BS-13132R-A488

Codice articolo locale: BOSSBS-13132R-A488

Descrizione: FAHD1 is a 224 amino acid protein belonging to the FAH family. Present as a homodimer, FAHD1 is thought to have hydrolase activity and uses magnesium and calcium as cofactors. The gene that encodes FAHD1 maps to human chromosome 16, which encodes over 900 genes in approximately 90 million base pairs, making up nearly 3% of human cellular DNA. 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, though through the CREBBP gene which encodes a critical CREB binding protein. Signs of Rubinstein-Taybi include mental retardation and predisposition to tumor growth and white blood cell neoplasias. Crohn's disease is a gastrointestinal inflammatory condition associated with chromosome 16 through the NOD2 gene. An association with systemic lupus erythematosis and a number of other autoimmune disorders with the pericentromeric region of chromosome 16 has led to the identification of SLC5A11 as a potential autoimmune modifier.

UOM: 1 * 100 µl

Promo

Codice catalogo: (PRSI56-326)

Fornitore: ProSci Inc.

Codice articolo fornitore: 56-326

Codice articolo locale: PRSI56-326

Descrizione: GRIN3B is a NMDA receptor subtype of glutamate-gated ion channels with reduced single-channel conductance, low calcium permeability and low voltage-dependent sensitivity to magnesium. It is mediated by glycine.

UOM: 1 * 400 µl

New Product Promo

Fornitore: MP Biomedicals

Descrizione: Soluble in water (1 g/3 ml - clear, colorless solution), boiling water (1 g/1,8 ml), glycerol (1 g/14 ml), or ethanol (1 g/250 ml); insoluble in ether or acetone; hydrochloric acid, sodium or magnesium chlorides diminish its solubility in water.

Certificati

Codice catalogo: (635-0247)

Fornitore: Atago

Codice articolo fornitore: 4443

Codice articolo locale: ATAG4443

Descrizione: The PAL series with special scales are pocket instruments delivering rapid results for automotive, aviation, heat transfer and industrial applications.

UOM: 1 * 1 pezzi

Promo