22509 Results for: "Hlavy+m\\\\u00EDchadel"

Supplier: Hach

These lightweight samplers with low power requirements (12 VDC) have been designed for easy mobility.

Supplier: Trajan Scientific and Medical

These GC ferrules are made from 100% PTFE. They are soft, completely inert, and have very low friction.

Supplier: KARTELL

PP, translucent urine cups with screw cap. Non sterile cups have a blue screw cap and are sold in multi-packs. Sterile cups have a red screw cap and a satinised marking area and are individually wrapped.

Supplier: Biotium

NucSpot® Live Cell Nuclear Stains are cell-membrane permeable DNA dyes that specifically stains nuclei in live or fixed cells. They have excellent specificity for DNA without the need for a wash step, and they have low toxicity for live cell imaging.

Supplier: AAT Bioquest

MP650 is designed to have identical spectra to those of Mustang Purple.

Supplier: Brady

Brady's B-430 clear polyester labels have been engineered to meet a large variety of performance needs.

Supplier: VWR Collection

VisiScope ALC microscopes have been designed to fulfil all the requirements of an advanced biology educational laboratory.

Supplier: BOCHEM

These burners have air regulation and reach a maximum temperature of 1300 °C.

Supplier: GRANT INSTRUMENTS

Grant blocks have a depth of 63 mm, ensuring precise temperature control for test tube applications.

Supplier: Brady

Prohibition signs must have a black diagram encircled by a red band and dissected by a red diagonal bar.

Supplier: MACHEREY-NAGEL

These shell vials for HPLC analyses have the advantage of an easy handling.

Supplier: AAT Bioquest

Although ROX dyes have strong fluorescence they are notoriously unstable.

Supplier: SEMADENI

These catheter syringes have a PP barrel with silicone rubber piston.

Supplier: MACHEREY-NAGEL

These screw neck vials have a wide opening for easy filling.

Supplier: AAT Bioquest

Melanins have very diverse roles and functions in various organisms.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: ProSci Inc.

PSG6 may have a role in modulation of the innate immune system.

Supplier: Brady

Lockouts for use on breakers that do not have a hole in the switch tongue, including multipole breakers with tie-bars.

Supplier: ESCHENBACH OPTIK

These illuminated magnifiers have a Ceratec® anti-scratch hard coating ensuring reliability, comfort and a relaxed vision.

Supplier: ENDECOTTS

These test sieves have a brass frame and stainless steel mesh.

Supplier: Bioss

Defects in G6PD are the cause of chronic non-spherocytic hemolytic anemia (CNSHA) . Deficiency of G6PD is associated with hemolytic anemia in two different situations. First, in areas in which malaria has been endemic, G6PD-deficiency alleles have reached high frequencies (1% to 50%) and deficient individuals, though essentially asymptomatic in the steady state, have a high risk of acute hemolytic attacks. Secondly, sporadic cases of G6PD deficiency occur at a very low frequencies, and they usually present a more severe phenotype. Several types of CNSHA are recognized. Class-I variants are associated with severe NSHA; class-II have an activity <10% of normal; class-III have an activity of 10% to 60% of normal; class-IV have near normal activity.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: AAT Bioquest

5-FITC and 6-FITC have very similar absorption and fluorescence spectra.

Supplier: Bioss

This gene, which encodes a member of the serine/threonine kinase family, regulates cell polarity and functions as a tumor suppressor. Mutations in this gene have been associated with Peutz-Jeghers syndrome, an autosomal dominant disorder characterised by the growth of polyps in the gastrointestinal tract, pigmented macules on the skin and mouth, and other neoplasms. Alternate transcriptional splice variants of this gene have been observed but have not been thoroughly characterised.

Supplier: HyClone products (Cytiva)

HyClone AdvanceSTEM ES Qualified Amino Acids have been optimized for growth of embryonic cell cultures.

Supplier: Bioss

Defects in G6PD are the cause of chronic non-spherocytic hemolytic anemia (CNSHA) . Deficiency of G6PD is associated with hemolytic anemia in two different situations. First, in areas in which malaria has been endemic, G6PD-deficiency alleles have reached high frequencies (1% to 50%) and deficient individuals, though essentially asymptomatic in the steady state, have a high risk of acute hemolytic attacks. Secondly, sporadic cases of G6PD deficiency occur at a very low frequencies, and they usually present a more severe phenotype. Several types of CNSHA are recognized. Class-I variants are associated with severe NSHA; class-II have an activity <10% of normal; class-III have an activity of 10% to 60% of normal; class-IV have near normal activity.

Supplier: IKA

The IKA Matrix Orbital Delta family of thermoshakers, with mixing and heating, have numerous user-friendly features.