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When normal cells are grown in culture they stop growing when they become overcrowded. This is called contact inhibition. Cancer cells in culture grow in an uncontrolled way because they have lost thi
According to the World Health Organization, between 2 and 3 million cases of skin cancer occur globally every year. Many of these cancers are caused by preventable damage to DNA by UV light during sun
Genetic modification of plants is a highly controversial area of biotechnology. All such experiments in plants begin with establishing plant cells in culture. This involves de-differentiating plant ce
Biological assays, or bioassays, are powerful tools that allow scientists to determine the effects of a given substance on living organisms. In this inquiry-based lab, students plan and perform a plan
Our all-new standard marker features better separation, easier band measurements, and no unused bands! DNA Standard ladder sizes, in base pairs: 6751, 3652, 2827, 1568, 1118, 825, 630. Includes: For 2
Place one BactoBead™ on the agar plate, watch it dissolve, and streak for isolated colonies. BactoBeads™ associated with the following kits: • EDVO-Kit #851 Effects of Alcohol on C. elegans • EDVO-Kit
E. coli GFP Host BactoBeads™ associated with the following kits: • EDVO-Kit #222 Transformation of E. coli with Blue and Green Fluorescent Proteins • EDVO-Kit #223/AP08 Transformation of E. coli with
E. coli host for transformation with pUC plasmids. BactoBeads™ associated with the following kits: • EDVO-Kit #221Transformation of E. coli with pGAL™ (Blue Colony) • EDVO-Kit #300 Blue/White Cloning
The approximate sizes of the λ / EcoR I and Hind III DNA fragments, in base pairs, are 22,000, 5000, 4500, 4000, 3500, 3000, 2000, 1500, 1000 (2 bands), and 500 (2 bands). A sample volume of 20 μl is
The sizes of the λ / EcoRI DNA fragments, in base pairs, are 21226, 7421, 5804, 5643, 4878, and 3530. A sample volume of 20 μl is recommended for ethidium bromide or SYBR Safe staining and 35-40 μl is
Tray is designed for use with the M12 Electrophoresis Apparatus, features an highlighted gel loading line and includes: (1) 14 x 7 cm Gel Tray and (2) Rubber End Caps *Not Compatible with Classic Comb
Tray is designed for use specifically with the Cat. #502-504 - M12 Electrophoresis Apparatus. *Not Compatible with Next Generation Combs or End Caps
The tris-glycine electrode buffer can be used for the electrophoresis of native, anionic proteins in polyacrylamide and agarose gels.
• (1) 4-20% Tris-Glycine-SDS Precast Polyacrylamide Gel (PAGE) • Size: 9 x 10 cm • Designed for Separating Protein Fragments 20-100 kDa • Each Gel Has 10 Wells • Well Volume is 30 µl • Requires Refrig
0.2 ml Thin-Walled PCR Microtest Tubes (Package of 100)
The media contains hydrolyzed casein, yeast extract and salts for the growth of bacteria. Twenty-five grams is added to every liter of distilled water. The liquid media is then autoclaved at 121˚C for
This powdered blend Tris-Borate EDTA buffer (TBE), has been optimized for agarose gel electrophoresis of nucleic acids. Dissolve powder in 500 ml of distilled or deionized water to prepare a 10x conce
Melt and Pour UltraSpec-Agarose™ consists of 0.8% electrophoretic grade UltraSpec-Agarose™ in tris-acetate-EDTA buffer, pH 7.9-8.0. The agarose concentration is sufficient for the separation of DNA fr
ABOUT THIS PRODUCT: Includes: (2) 7 x 7 cm Gel Trays, (2) 6 Tooth Combs & (2) Sets of Rubber End Caps
Compact and easy to use, yet powerful enough to enable each workstation to be equipped with a centrifuge for a wide range of molecular biology separations and quick spins. • Compact footprint and brus
The EDGE™ Integrated Electrophoresis System revolutionizes biotechnology by merging an electrophoresis chamber, power supply and blue light into a single, safe and easy-to-use apparatus. It runs a 10
In this experiment, students will gain an understanding of the traditional three-step Polymerase Chain Reaction (PCR). Using PCR and Agarose Gel Electrophoresis, they will analyze a small section of L
Reverse-transcription PCR (RT-PCR) is the gold standard for the detection of SARS-CoV-2 due to the sensitivity, specificity, and feasibility of the test. In this simulated RT-PCR experiment, students
In Western blot analysis, protein identification is based on antibody and antigen reactions. Proteins are separated on polyacrylamide gels and are transferred (blotted) to a nylon membrane. The membra
Four experimental modules are combined into one experiment to provide a comprehensive biotechnology exploration focusing on the green fluorescent protein (GFP). Bacterial cells are transformed to expr
This easy and safe experiment allow your students to learn about enzyme catalysis, the nature of enzyme action and protein structure-function relationships. Students will perform an enzyme assay and d
In this experiment, students will perform an Enzyme-Linked Immunosorbent Assay (ELISA) to examine the impact of this powerful test on human health. Antibodies will be used to detect minuscule amounts
The second assay used to confirm a positive HIV ELISA result is the Western Blot. Students separate protein samples from hypothetical patients on agarose gels, transfer the samples to a membrane and d
In this experiment, students will perform an enzyme-linked immunosorbent assay (ELISA) in order to screen simulated serum samples for antibodies to the Epstein Barr Virus (EBV) - a virus that causes m
The carbon dioxide detector measures Carbon Dioxide (CO2), air temperature and humidity. The device helps measure ventilation in enclosed spaces such as classrooms, offices, and hospitality venues, an
ABOUT THIS PRODUCT: Most molecules have a net charge within a pH range of 2 to 10. When the pH is altered, the net charge on molecules can change drastically. In this experiment, a mixture of two chem
At the intersection of art, science, and technology is Bio-Art, the creation of works of art using living matter. One common way to create Bio-Art uses bacteria transformed with DNA codes for brightly
The DNA from bacteriophage lambda is a well-characterized linear molecule containing six recognition sites for Eco RI (generating 5 fragments with distinct sizes and 2 fragments that are very close in
Explore cutting-edge biotechnology with this hands-on CRISPR-Cas9 simulation. Students will assume the role of plant geneticists working to develop corn crops capable of surviving, and thriving, in a
In this experiment, students explore the effects of DNA methylation on restriction enzyme activity. Plasmid DNA will be digested with the restriction enzymes DpnI and DpnII. When digested with these e
This experiment introduces your students to Southern blotting as a tool for 'DNA Fingerprinting' in a hypothetical paternity determination. DNA fragments are first separated by agarose gel electrophor
Isolation of high molecular weight chromosomal DNA is the first step in molecular cloning since it is the source of genes in cells. This experiment provides DNA Extraction LyphoCells™ and reagents for
Trace amounts of blood are often sufficient to identify the individual responsible for any number of crimes, including murder, burglary, or assault. Enhancement procedures can make a small stain of bo
Gram staining is a quick, effective, and medically relevant identification test that has beome one of the most essential tools in bacterial classification. In this experiment, students will use this s
LyphoProtein™ Samples for 12 Groups • Store Desiccated @ -20° C • Use within 6 months of receipt
Cancer cells differ from normal cells by the combinations of proteins that are present on their surfaces. Antibodies against these proteins will specifically bind to cancer cells and not to normal cel
Showing products per page
When normal cells are grown in culture they stop growing when they become overcrowded. This is called contact inhibition. Cancer cells in culture grow in an uncontrolled way because they have lost thi
According to the World Health Organization, between 2 and 3 million cases of skin cancer occur globally every year. Many of these cancers are caused by preventable damage to DNA by UV light during sun
Genetic modification of plants is a highly controversial area of biotechnology. All such experiments in plants begin with establishing plant cells in culture. This involves de-differentiating plant ce
Biological assays, or bioassays, are powerful tools that allow scientists to determine the effects of a given substance on living organisms. In this inquiry-based lab, students plan and perform a plan
Our all-new standard marker features better separation, easier band measurements, and no unused bands! DNA Standard ladder sizes, in base pairs: 6751, 3652, 2827, 1568, 1118, 825, 630. Includes: For 2
Place one BactoBead™ on the agar plate, watch it dissolve, and streak for isolated colonies. BactoBeads™ associated with the following kits: • EDVO-Kit #851 Effects of Alcohol on C. elegans • EDVO-Kit
E. coli GFP Host BactoBeads™ associated with the following kits: • EDVO-Kit #222 Transformation of E. coli with Blue and Green Fluorescent Proteins • EDVO-Kit #223/AP08 Transformation of E. coli with
E. coli host for transformation with pUC plasmids. BactoBeads™ associated with the following kits: • EDVO-Kit #221Transformation of E. coli with pGAL™ (Blue Colony) • EDVO-Kit #300 Blue/White Cloning
The approximate sizes of the λ / EcoR I and Hind III DNA fragments, in base pairs, are 22,000, 5000, 4500, 4000, 3500, 3000, 2000, 1500, 1000 (2 bands), and 500 (2 bands). A sample volume of 20 μl is
The sizes of the λ / EcoRI DNA fragments, in base pairs, are 21226, 7421, 5804, 5643, 4878, and 3530. A sample volume of 20 μl is recommended for ethidium bromide or SYBR Safe staining and 35-40 μl is
Tray is designed for use with the M12 Electrophoresis Apparatus, features an highlighted gel loading line and includes: (1) 14 x 7 cm Gel Tray and (2) Rubber End Caps *Not Compatible with Classic Comb
Tray is designed for use specifically with the Cat. #502-504 - M12 Electrophoresis Apparatus. *Not Compatible with Next Generation Combs or End Caps
The tris-glycine electrode buffer can be used for the electrophoresis of native, anionic proteins in polyacrylamide and agarose gels.
• (1) 4-20% Tris-Glycine-SDS Precast Polyacrylamide Gel (PAGE) • Size: 9 x 10 cm • Designed for Separating Protein Fragments 20-100 kDa • Each Gel Has 10 Wells • Well Volume is 30 µl • Requires Refrig
0.2 ml Thin-Walled PCR Microtest Tubes (Package of 100)
The media contains hydrolyzed casein, yeast extract and salts for the growth of bacteria. Twenty-five grams is added to every liter of distilled water. The liquid media is then autoclaved at 121˚C for
This powdered blend Tris-Borate EDTA buffer (TBE), has been optimized for agarose gel electrophoresis of nucleic acids. Dissolve powder in 500 ml of distilled or deionized water to prepare a 10x conce
Melt and Pour UltraSpec-Agarose™ consists of 0.8% electrophoretic grade UltraSpec-Agarose™ in tris-acetate-EDTA buffer, pH 7.9-8.0. The agarose concentration is sufficient for the separation of DNA fr
ABOUT THIS PRODUCT: Includes: (2) 7 x 7 cm Gel Trays, (2) 6 Tooth Combs & (2) Sets of Rubber End Caps
Compact and easy to use, yet powerful enough to enable each workstation to be equipped with a centrifuge for a wide range of molecular biology separations and quick spins. • Compact footprint and brus
The EDGE™ Integrated Electrophoresis System revolutionizes biotechnology by merging an electrophoresis chamber, power supply and blue light into a single, safe and easy-to-use apparatus. It runs a 10
In this experiment, students will gain an understanding of the traditional three-step Polymerase Chain Reaction (PCR). Using PCR and Agarose Gel Electrophoresis, they will analyze a small section of L
Reverse-transcription PCR (RT-PCR) is the gold standard for the detection of SARS-CoV-2 due to the sensitivity, specificity, and feasibility of the test. In this simulated RT-PCR experiment, students
In Western blot analysis, protein identification is based on antibody and antigen reactions. Proteins are separated on polyacrylamide gels and are transferred (blotted) to a nylon membrane. The membra
Four experimental modules are combined into one experiment to provide a comprehensive biotechnology exploration focusing on the green fluorescent protein (GFP). Bacterial cells are transformed to expr
This easy and safe experiment allow your students to learn about enzyme catalysis, the nature of enzyme action and protein structure-function relationships. Students will perform an enzyme assay and d
In this experiment, students will perform an Enzyme-Linked Immunosorbent Assay (ELISA) to examine the impact of this powerful test on human health. Antibodies will be used to detect minuscule amounts
The second assay used to confirm a positive HIV ELISA result is the Western Blot. Students separate protein samples from hypothetical patients on agarose gels, transfer the samples to a membrane and d
In this experiment, students will perform an enzyme-linked immunosorbent assay (ELISA) in order to screen simulated serum samples for antibodies to the Epstein Barr Virus (EBV) - a virus that causes m
The carbon dioxide detector measures Carbon Dioxide (CO2), air temperature and humidity. The device helps measure ventilation in enclosed spaces such as classrooms, offices, and hospitality venues, an
ABOUT THIS PRODUCT: Most molecules have a net charge within a pH range of 2 to 10. When the pH is altered, the net charge on molecules can change drastically. In this experiment, a mixture of two chem
At the intersection of art, science, and technology is Bio-Art, the creation of works of art using living matter. One common way to create Bio-Art uses bacteria transformed with DNA codes for brightly
The DNA from bacteriophage lambda is a well-characterized linear molecule containing six recognition sites for Eco RI (generating 5 fragments with distinct sizes and 2 fragments that are very close in
Explore cutting-edge biotechnology with this hands-on CRISPR-Cas9 simulation. Students will assume the role of plant geneticists working to develop corn crops capable of surviving, and thriving, in a
In this experiment, students explore the effects of DNA methylation on restriction enzyme activity. Plasmid DNA will be digested with the restriction enzymes DpnI and DpnII. When digested with these e
This experiment introduces your students to Southern blotting as a tool for 'DNA Fingerprinting' in a hypothetical paternity determination. DNA fragments are first separated by agarose gel electrophor
Isolation of high molecular weight chromosomal DNA is the first step in molecular cloning since it is the source of genes in cells. This experiment provides DNA Extraction LyphoCells™ and reagents for
Trace amounts of blood are often sufficient to identify the individual responsible for any number of crimes, including murder, burglary, or assault. Enhancement procedures can make a small stain of bo
Gram staining is a quick, effective, and medically relevant identification test that has beome one of the most essential tools in bacterial classification. In this experiment, students will use this s
LyphoProtein™ Samples for 12 Groups • Store Desiccated @ -20° C • Use within 6 months of receipt
Cancer cells differ from normal cells by the combinations of proteins that are present on their surfaces. Antibodies against these proteins will specifically bind to cancer cells and not to normal cel
Showing products per page