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2\'-Deoxyuridine-5\'-triphosphate+trisodium+salt
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2\'-Deoxyuridine-5\'-triphosphate+trisodium+salt
Lieferant:
Sigma-Aldrich
Beschreibung:
Non-selective P2 purinoceptor antagonist which blocks responses at both pre-junctional and post-junctional sites.
Artikel-Nr:
(573115-50)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
573115-50
Lokale Artikelnummer::
CALB573115-50
Beschreibung:
SMCC, Water-Soluble, a water-soluble derivative of SMCC.
VE:
1 * 50 mg
Artikel-Nr:
(116802-10)
Lieferant:
Merck Millipore (Calbiochem)
Hersteller-Artikelnummer::
116802-10
Lokale Artikelnummer::
CALB116802-10
Beschreibung:
A potent cell-permeable activator of cAMP-dependent protein kinase (PKA). Due to its considerably increased lipophilicity, it has sufficient membrane permeability for many biological systems.
VE:
1 * 10 µmol
Lieferant:
MP Biomedicals
Beschreibung:
Dextran sulfate is a polyanionic derivative of dextran produced by esterification of Dextran with chlorosulphonic acid. Dextran sulfate sodium (DSS) is the sodium salt which is a white to off-white powder freely soluble in water and salt solutions to form a stable, clear solution. The high purity and reproducible quality enables its application in pharmaceuticals and biotechnology industry.
Lieferant:
APOLLO SCIENTIFIC
Beschreibung:
An aminoglycoside antibiotic with bactericidal activity
Artikel-Nr:
(BOSSBS-9847R-A680)
Lieferant:
Bioss
Hersteller-Artikelnummer::
BS-9847R-A680
Lokale Artikelnummer::
BOSSBS-9847R-A680
Beschreibung:
Primary canalicular bile undergoes a process of fluidization and alkalinization along the biliary tract that is influenced by several factors, including hormones, innervation/neuropeptides and biliary constituents. The excretion of bicarbonate at both the canaliculi and the bile ducts is an important contributor to the generation of bile-salt independent flow. Bicarbonate is secreted from hepatocytes and cholangiocytes through parallel mechanisms, which involve chloride efflux through activation of chloride channels and further bicarbonate secretion via AE2 (also designated SLC4A2)-mediated chloride/bicarbonate exchange. The AE2 protein regulates pH, chloride concentration, cell volume and transepithelial ion transport in many tissues. Gene silencing of AE2 causes a marked inhibition of unstimulated and secretin-stimulated chloride/bicarbonate exchange, which maintains the bile acid pool that is crucial for secretin to induce bicarbonate-rich choleresis.
VE:
1 * 100 µl
Lieferant:
Thermo Scientific
Beschreibung:
1-Pentansulfonsäure Natriumsalz, wasserfrei 99+% für die Ionenpaar-Chromatographie
Lieferant:
MP Biomedicals
Beschreibung:
Deoxyribonucleic acid is a polynucleotide . It is an essential component of chromosomes in cell nuclei. It is the carrier of genetic material. It contains information in chemical code to direct the development of the cell according to its inheritance. The purine and pyrimidine bases of the nucleosides are primarily adenine, guanine, cytosine and thymine. The sugar is D-2-deoxyribose.
Artikel-Nr:
(MOLE38417956-25G)
Lieferant:
Molekula
Hersteller-Artikelnummer::
38417956-25G
Lokale Artikelnummer::
MOLE38417956-25G
Beschreibung:
Dextransulfat Natriumsalz
VE:
1 * 25 g
 This is a MarketSource item. Additional charges may apply
Lieferant:
MP Biomedicals
Beschreibung:
Dextran sulphate is a polyanionic derivative of dextran produced by esterification of Dextran with chlorosulphonic acid. Dextran sulphate sodium (DSS) is the sodium salt which is a white to off-white powder freely soluble in water and salt solutions to form a stable, clear solution. The sulphur content is approximately 17% which corresponds to an average of 1.9 sulphate groups per glucosyl residue of the dextran molecule.
Artikel-Nr:
(J63456.X0)
Lieferant:
Alfa Aesar
Hersteller-Artikelnummer::
J63456.X0
Lokale Artikelnummer::
ALFAJ63456.X0
Beschreibung:
Phosphoramidon (disodium salt)
VE:
1 * 5 mg
Lieferant:
Biotium
Beschreibung:
The epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Lieferant:
Biotium
Beschreibung:
The epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Lieferant:
Biotium
Beschreibung:
The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Lieferant:
Biotium
Beschreibung:
The epitope of this MAb maps in the N-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
Lieferant:
Biotium
Beschreibung:
The epitope of this MAb maps in the C-terminus of PTH, a hormone produced by the parathyroid gland that regulates the concentration of calcium and phosphorus in extracellular fluid. This hormone elevates blood Ca2 levels by dissolving the salts in bone and preventing their renal excretion.It is produced in the parathyroid gland as an 84 amino acid single chain polypeptide. It can also be secreted as N-terminal truncated fragments or C-terminal fragments after intracellular degradation, as in case of hypercalcemia. Defects in this gene are a cause of familial isolated hypoparathyroidism (FIH); also called autosomal dominant hypoparathyroidism or autosomal dominant hypocalcemia. FIH is characterized by hypocalcemia and hyperphosphatemia due to inadequate secretion of parathyroid hormone. Symptoms are seizures, tetany and cramps. FIH exist both as autosomal dominant and recessive forms of hypoparathyroidism.
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 noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
Lager für diesen Artikel ist begrenzt, kann aber in einem Lagerhaus in Ihrer Nähe zur Verfügung. Bitte stellen Sie sicher, dass Sie in sind angemeldet auf dieser Seite, so dass verfügbare Bestand angezeigt werden können. Wenn das
noch angezeigt wird und Sie Hilfe benötigen, rufen Sie uns an 1-800-932 - 5000.
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