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Hai cercato: Magnesium+tetraborate


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


Codice catalogo: (BOSSBS-9734R-CY7)
Fornitore: Bioss
Codice articolo fornitore: BS-9734R-CY7
Codice articolo locale: BOSSBS-9734R-CY7
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


Codice catalogo: (BOSSBS-9734R-HRP)
Fornitore: Bioss
Codice articolo fornitore: BS-9734R-HRP
Codice articolo locale: BOSSBS-9734R-HRP
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


Codice catalogo: (BOSSBS-9734R-FITC)
Fornitore: Bioss
Codice articolo fornitore: BS-9734R-FITC
Codice articolo locale: BOSSBS-9734R-FITC
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


Codice catalogo: (BOSSBS-9734R-A488)
Fornitore: Bioss
Codice articolo fornitore: BS-9734R-A488
Codice articolo locale: BOSSBS-9734R-A488
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


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: (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


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
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


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: (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: (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


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

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
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: 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.

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