"Liners+gc+septa+gc+ferrules"

Supplier: Agilent

These inlet seals have been developed to ensure that you have a consistent and inert surface to properly seal the inlet and prevent sample degradation.

Supplier: VARIAN

Clean PP reservoirs contain two PP frits pre-inserted, an ideal configuration for simple filtration.

Supplier: INTERCHIM

These flash chromatography columns with high performance silica are suitable for the purification non-ionic polar organic compounds.

Supplier: DR MAISCH

Speziell entwickelt für pharmazeutische und biotechnologische Trennungen. Ideal für LC-MS-Trennungen.

Supplier: ISERA

A maximum of separation efficiency and perfect selectivity comply with highest demands.

Supplier: Resonac

These are styrene divinylbenzene copolymer-based organic solvent SEC (GPC) columns. Suitable for a wide range of applications from low to high molecular weight compounds.

Supplier: VARIAN

Polaris™ silica is ideal for the rapid separation of low molecular weight compounds that are soluble in organic solvents.

Supplier: Cytiva

His SpinTrap™ is a prepacked, single use spin column for purifying histidine-tagged proteins by immobilised metal ion affinity chromatography (IMAC) and rapid expression screening.

Supplier: Cytiva

HiTrap™ Octyl FF are prepacked Octyl Sepharose™ 4 Fast Flow columns for hydrophobic interaction chromatography (HIC).

Supplier: PerkinElmer

Small pore silica-based sorbent used for separation of small molecules. Non-functional and polyfunctional C8 and C18 are available.

Supplier: Bioss

EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

Supplier: Bioss

EVC is an autosomal skeletal dysplasia caused by mutations in the EVC and EVC2 genes. Found in developing ribs, heart, kidney and lung, the EVC gene is responsible for normal development of the face, limbs, teeth and nails. The protein expressed by the EVC gene is an intracellular component of the hedgehog signal pathway that contains a leucine zipper and transmembrane domain. Defects in the EVC gene can lead to short-limb dwarfism, ectodermal dysplasia and cardiac anomalies such as irregular atrioventricular septum development. Additionally, the EVC gene has been implicated in Weyers acrodental dysostosis, an autosomal dominant disease characterized by facial abnormalities and limb defects.

Supplier: Thermo Fisher Scientific

Erzielen Sie schnelle, hochauflösende Trennungen aromatischer Verbindungen mit Thermo Scientific™ Accucore Phenyl-X-Säulen.

Supplier: Cytiva

HiScreen™ Capto™ L columns are prepacked with Capto™ L, an affinity chromatography medium (resin) for capture of antibodies and antibody fragments such as Fab fragments, scFv, and Dabs.

Supplier: MACHEREY-NAGEL

NUCLEOSIL® C4 is butyl modified silica phase for HPLC.

Supplier: MACHEREY-NAGEL

NUCLEOSIL® C2 is a dimethyl modified silica phase for HPLC.