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Producto Referencia Descripción Formato PDF Detalles
StayBrite™ D-Luciferin, Potassium Salt 7903-100 C11H7KN2O3S2... 100 mg N/D
StayBrite™ D-Luciferin, Potassium Salt » Descripción

C11H7KN2O3S2

» Información

A useful substrate for the enzyme Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence.

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Shipping: gel pack, Storage Temp.: -20°C

StayBrite™ D-Luciferin, Sodium Salt 7902-10G C₁₁H₇N₂O₃S₂. Na... 10 g N/D
StayBrite™ D-Luciferin, Sodium Salt » Descripción

C₁₁H₇N₂O₃S₂. Na

» Información

A useful substrate for the enzyme Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence.

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Shipping: gel pack, Storage Temp.: -20°C

StayBrite™ D-Luciferin, Sodium Salt 7902-1G C₁₁H₇N₂O₃S₂. Na... 1 g N/D
StayBrite™ D-Luciferin, Sodium Salt » Descripción

C₁₁H₇N₂O₃S₂. Na

» Información

A useful substrate for the enzyme Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence.

» Más Datos

Shipping: gel pack, Storage Temp.: -20°C

StayBrite™ D-Luciferin, Sodium Salt 7902-100 C₁₁H₇N₂O₃S₂. Na... 100 mg N/D
StayBrite™ D-Luciferin, Sodium Salt » Descripción

C₁₁H₇N₂O₃S₂. Na

» Información

A useful substrate for the enzyme Luciferase. Upon oxidation by the enzyme luciferase, produces bioluminescence.

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Shipping: gel pack, Storage Temp.: -20°C

CFTR Inhibitor-172 2487-5 C₁₈H₁₀F₃NO₃S₂... 5 mg N/D
CFTR Inhibitor-172 » Descripción

C₁₈H₁₀F₃NO₃S₂

» Información

A potent, reversible, selective, CFTR chloride channel blocker. Inhibits CFTR short-circuit current in < 2 minutes in a voltage-independent manner (Ki = ~ 300 nM). At concentrations fully inhibiting CFTR, CFTR(inh)-172 does not block increase of cellular cAMP or inhibit non-CFTR Cl(-) channels, multidrug resistance protein-1 (MDR-1), ATP-sensitive K(⁺) channels, or a series of other transporters.

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Shipping: gel pack, Storage Temp.: - 20°C

CFTR Inhibitor-172 2487-1 C₁₈H₁₀F₃NO₃S₂... 1 mg N/D
CFTR Inhibitor-172 » Descripción

C₁₈H₁₀F₃NO₃S₂

» Información

A potent, reversible, selective, CFTR chloride channel blocker. Inhibits CFTR short-circuit current in < 2 minutes in a voltage-independent manner (Ki = ~ 300 nM). At concentrations fully inhibiting CFTR, CFTR(inh)-172 does not block increase of cellular cAMP or inhibit non-CFTR Cl(-) channels, multidrug resistance protein-1 (MDR-1), ATP-sensitive K(⁺) channels, or a series of other transporters.

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Shipping: gel pack, Storage Temp.: - 20°C

Chloramphenicol 2486-500G C₁₁H₁₂Cl₂N₂O₅... 500 g N/D
Chloramphenicol » Descripción

C₁₁H₁₂Cl₂N₂O₅

» Información

Chloramphenicol is a bacteriostatic antibiotic that inhibits bacterial protein synthesis. Displays a broad spectrum antibiotic activity targeting a wide variety of gram positive and gram negative bacteria especially those which cause meningitis. Used as a seletion agent for transformed cells containing chloramphenicol resistance genes.

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Shipping: RT, Storage Temp.: + 4°C

Chloramphenicol 2486-100G C₁₁H₁₂Cl₂N₂O₅... 100 g N/D
Chloramphenicol » Descripción

C₁₁H₁₂Cl₂N₂O₅

» Información

Chloramphenicol is a bacteriostatic antibiotic that inhibits bacterial protein synthesis. Displays a broad spectrum antibiotic activity targeting a wide variety of gram positive and gram negative bacteria especially those which cause meningitis. Used as a seletion agent for transformed cells containing chloramphenicol resistance genes.

» Más Datos

Shipping: RT, Storage Temp.: + 4°C

Chloramphenicol 2486-25G C₁₁H₁₂Cl₂N₂O₅... 25 g N/D
Chloramphenicol » Descripción

C₁₁H₁₂Cl₂N₂O₅

» Información

Chloramphenicol is a bacteriostatic antibiotic that inhibits bacterial protein synthesis. Displays a broad spectrum antibiotic activity targeting a wide variety of gram positive and gram negative bacteria especially those which cause meningitis. Used as a seletion agent for transformed cells containing chloramphenicol resistance genes.

» Más Datos

Shipping: RT, Storage Temp.: + 4°C

Beta-Secretase Inhibitor II 7502-1 C₂₅H₃₉N₃O₅... 1 mg N/D
Beta-Secretase Inhibitor II » Descripción

C₂₅H₃₉N₃O₅

» Información

A potent, cell permeable and reversible inhibitor of β-secretase that corresponds to the β-secretase cleavage site (VNL-DA) of the Swedish mutant Amyloid Precursor Protein (APP). Inhibits the formation of both Aβtotal (IC₅₀ = 700 nM) and Aβ1-42 (IC₅₀ = 2.5 µM) in CHO cells stably transfected with wild-type APP751.

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Shipping: gel pack, Storage Temp.: -20°C

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