Hai cercato: Magnesium+tetraborate

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

Promo

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

Promo

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

Promo

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

Promo

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

Promo

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: (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

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: (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: (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

Promo

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

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: 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

Certificati

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: 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.