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Image Unavailable-BOSSBS-12039R-CY3

Anti-GDE1 Rabbit Polyclonal Antibody (Cy3®)

Descripción: 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.
Numero del catalogo: BOSSBS-12039R-CY3
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-12039R-A555

Anti-GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 555)

Descripción: 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.
Numero del catalogo: BOSSBS-12039R-A555
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-BOSSBS-12039R-A647

Anti-GDE1 Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Descripción: 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.
Numero del catalogo: BOSSBS-12039R-A647
UOM: 1 * 100 µl
Proveedor: Bioss
Product Image-HYCLSH30258.01

Phosphate buffered saline solutions (PBS) without calcium and magnesium, HyClone™

Descripción: Balanced salt solution used for multiple cell culture applications.
Numero del catalogo: HYCLSH30258.01
UOM: 1 * 500 mL
Proveedor: HyClone products (Cytiva)

Certificados


Image Unavailable-BOSSBS-12039R-CY5

Anti-GDE1 Rabbit Polyclonal Antibody (Cy5®)

Descripción: 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.
Numero del catalogo: BOSSBS-12039R-CY5
UOM: 1 * 100 µl
Proveedor: Bioss
Image Unavailable-04260-30KG

Hidrogenoortofosfato de magnesio trihidrato ≥98%, Puriss. special, meets analytical specification of DAB, Fluka™

Descripción: Hidrogenoortofosfato de magnesio trihidrato ≥98%, Puriss. special, meets analytical specification of DAB, Fluka™
Numero del catalogo: 04260-30KG
UOM: 1 * 30 kg
Proveedor: Honeywell Chemicals
Image Unavailable-ICNA092820549

EDTA disodium salt solution, 0,2% in phosphate buffered saline, MP Biomedicals

Descripción: EDTA disodium salt, (2%) solution, in phosphate buffered saline without calcium and magnesium. Used as a gentle non-enzymatic cell dissociation reagent.
Numero del catalogo: ICNA092820549
UOM: 1 * 100 mL
Proveedor: MP Biomedicals
Product Image-21-040-CM

Phosphate-buffered saline (PBS), Corning®

Descripción: Phosphate buffered saline (PBS) is a buffer solution containing sodium chloride, sodium phosphate, and in some formulations potassium chloride and potassium phosphate
Numero del catalogo: 21-040-CM
UOM: 1 * 6 UN
Proveedor: Corning

Certificados


Product Image-21-031-CM

Dulbecco's phosphate-buffered saline (DPBS), Corning®

Descripción: 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
Numero del catalogo: 21-031-CM
UOM: 1 * 6 UN
Proveedor: Corning

Certificados


Product Image-ICNA091860449

Dulbecco's phosphate buffered saline (DPBS), cell culture, MP Biomedicals

Descripción: 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.
Numero del catalogo: ICNA091860449
UOM: 1 * 100 mL
Proveedor: MP Biomedicals

FDS


Product Image-PRSI26-095

Anti-MTHFD2 Rabbit Polyclonal Antibody

Descripción: This protein is a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. This gene encodes a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. Alternative splicing results in multiple transcripts encoding different isoforms. This gene has a pseudogene on chromosome 7.
Numero del catalogo: PRSI26-095
UOM: 1 * 50 µG
Proveedor: ProSci Inc.
Product Image-PRSI30-142

Anti-MTHFD2 Rabbit Polyclonal Antibody

Descripción: MTHFD2 is a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD.This gene encodes a nuclear-encoded mitochondrial bifunctional enzyme with methylenetetrahydrofolate dehydrogenase and methenyltetrahydrofolate cyclohydrolase activities. The enzyme functions as a homodimer and is unique in its absolute requirement for magnesium and inorganic phosphate. Formation of the enzyme-magnesium complex allows binding of NAD. Alternative splicing results in multiple transcripts encoding different isoforms. This gene has a pseudogene on chromosome 7.
Numero del catalogo: PRSI30-142
UOM: 1 * 100 µG
Proveedor: ProSci Inc.
Product Image-HACH1430598

Buffer solution for water testing

Descripción: Buffered dilution water required for testing recreational, drinking and wastewater.
Numero del catalogo: HACH1430598
UOM: 1 * 25 UN
Proveedor: Hach
Product Image-STMC37350

Dulbecco's Phosphate Buffered Saline (D-PBS) without Ca++ and Mg++

Descripción: Dulbecco’s phosphate-buffered saline (D-PBS) can be used as a temporary diluting, washing, irrigating or transporting solution for cell or tissue culture. It provides a buffering system to maintain the physiological pH range and osmotic balance of culture media and provides cells with a source of water and essential inorganic ions.
Numero del catalogo: STMC37350
UOM: 1 * 500 mL
Proveedor: STEMCELL Technologies
Product Image-STMC37354

Dulbecco's Phosphate Buffered Saline (D-PBS), 10X Concentrate without Ca++ and Mg++

Descripción: Dulbecco’s phosphate-buffered saline (D-PBS) can be used as a temporary diluting, washing, irrigating or transporting solution for cell or tissue culture. It provides a buffering system to maintain the physiological pH range and osmotic balance of culture media and provides cells with a source of water and essential inorganic ions.
Numero del catalogo: STMC37354
UOM: 1 * 500 mL
Proveedor: STEMCELL Technologies
Image Unavailable-PRSI91-214

Human recombinant Inositol Monophosphatase 1 (from E. coli)

Descripción: Inositol Monophosphatase 1 (IMPA1) belongs to the inositol monophosphatase family. IMPA1 is responsible for the provision of inositol required for synthesis of phosphatidylinositol and polyphosphoinositides, IMPA1 can use myo-inositol-1,3-diphosphate, myo-inositol-1,4-diphosphate, scyllo-inositol-phosphate, glucose-1-phosphate, glucose-6-phosphate, fructose-1-phosphate, beta-glycerophosphate, and 2-AMP as substrates. IMPA1 has been implicated as the pharmacological target for lithium action in brain. IMPA1 shows magnesium-dependent phosphatase activity and is inhibited by therapeutic concentrations of lithium. In addition, IMPA1 plays a improtant role in intracellular signal transduction.
Numero del catalogo: PRSI91-214
UOM: 1 * 50 µG
Proveedor: ProSci Inc.
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