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Plasmid and lambda DNA are pre-digested with restriction enzymes - endonucleases that recognize and cut double-stranded DNA within or near defined base sequences. Digests are separated by agarose gel
Plasmid and lambda DNA are pre-digested with restriction enzymes - endonucleases that recognize and cut double-stranded DNA within or near defined base sequences. Digests are separated by agarose gel
Product Features: Cast iron hotplate Variable heat settings Overheat protection Corrosion resistant Power indicator Easy clean finish Non-slip rubber feet Hotplate diameter: 185mm Powe
These unstirred water baths are ideal for general laboratory use and are economical, reliable and very cost effective. Comprising of a high quality corrosion resistant seamless stainless steel tank, with a bright clean finish housed in a durable p
The DuoSource™ is our most popular electrophoresis power supply and runs gels quickly - in only 20-30 minutes at 150 V! Features: • Max Voltage: 150 Volts • Voltage Steps: 75 or 150 Volts • Max Curren
The successor to the bestselling EdvoCycler™ has been redesigned with improved PCR technology to be the best value among classroom thermal cyclers. The EdvoCycler™ 2 doubles the capacity of the origin
In this experiment, students will explore the biological process of bacterial transformation using E. coli and plasmid DNA. At the end of the activity, students will have experience observing and anal
In this experiment, your students will develop an understanding of bacterial transformation by plasmid DNA by introducing an opportunity to observe an acquired phenotypic trait of the transformed bact
FlashBlue™ is a proprietary DNA stain that offers simple and rapid staining of agarose gels. FlashBlue™ is provided as a concentrated liquid stain that, when diluted, can be used for both rapid and ov
This 50-fold concentrated Tris-Acetate EDTA buffer (TAE), pH 7.8-8.0, has been optimized for agarose gel electrophoresis of nucleic acids. One volume of buffer is added to every 49 volumes of distille
A cost affective way to introduce DNA electrophoresis to the classroom. The set provides all the equipment you need to run any DNA or dye electrophoresis kits with your students. Kit includes 1 x Hexa
Teach your students about restriction enzyme digests in the context of forensic science! Your students will cut DNA with restriction enzymes and then compare the banding pattern of the crime scene DNA
Give your students the opportunity to carry out PCR in the classroom! This kit provides easy to follow instructions for your students to develop various crime scene scenarios independently. Plasmid DN
This simple lab demonstrates detection of the mutation that causes Sickle Cell Anemia. In this simulation, your students will use electrophoresis to separate dyes that represent patient samples and co
Demonstrate how electrophoresis separates molecules on the basis of size and charge. A safe, colorful, fast and simple way to teach a technique that will engage your students. • Explore how gel electr
DNA obtained from a single hair left behind at a crime scene can be used to identify a criminal. In this experiment, your students will compare simulated crime scene DNA with that of two suspects. • L
Your class will make the invisible, visible! With this kit, your students will sample water and air and then grow any microbes present overnight. A safe and simple way to teach pollution. Group Size:
Investigate how agarose gel electrophoresis unlocks the color code used by food scientists to make colorful candies. Students will extract color activities from common candies and separate the dyes on
Your students can construct DNA models and then extract DNA from onions, strawberries or bananas. You provide the fruit or vegetables and 95-100% isopropyl alcohol, your students extract DNA. • Learn
After a crime has been committed, the evidence left behind can identify a potential culprit, although a single piece of evidence is not usually enough to convict someone. Even in this age of DNA, fing
The principles of diffusion and osmosis are applied to the movement of water within plants. Emphasis is given to water potential transport and the effect of the plant environment on transpiration. Gro
In this experiment, students will explore the biological process of bacterial transformation using E. coli and plasmid DNA. At the end of the activity, students will have experience observing and anal
Analysis of Eco RI Cleavage Patterns of Lambda DNA This experiment introduces the use of restriction enzymes as a tool to digest DNA at specific nucleotide sequences. Bateriophage lambda DNA has a lin
In this experiment, students will learn how to measure the rate of photosynthesis indirectly by studying the floating leaf disk assay, and test different variables that might affect the photosynthesis
ABOUT THIS PRODUCT: 1 EdvoCycler™ 2 (48 x 0.2 ml) 6 M12 Complete™ Package (14 x 7 cm Tray & 7 x 7 cm Trays (2) 3 QuadraSource™ Power Supply (10-300V, for 1 to 4 units) 6 Variable MicroPipette (5 - 50
This LabStation™ includes the following: 1 EdvoCycler™ Jr. (16 x 0.2 ml) 2 M12 Complete™ Package (14 x 7 cm Tray & 7 x 7 cm Trays (2) 1 QuadraSource™ Power Supply (10-300V, for 1 to 4 units) 2 Variabl
M12 Complete™ Electrophoresis Pac DuoSource™ 150 Power Supply (75 V or 150 V for 1 or 2 units) Fixed Volume MiniPipette (35 µl) Yellow Micropipet Tips(1 - 200 µl /2 Racks of 96) Whose DNA Was Left Beh
Protein InstaStain® sheets stain gels faster than conventional methods. Protein InstaStain® gives high quality and uniform gel staining with excellent results for photography. They are also environmen
Are you planning a virtual curriculum or looking for experiments ideal for distance learning? With MyLab™ custom kits from Edvotek, you can plan your curriculum and have all the materials sent directl
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
Showing products per page
Plasmid and lambda DNA are pre-digested with restriction enzymes - endonucleases that recognize and cut double-stranded DNA within or near defined base sequences. Digests are separated by agarose gel
Plasmid and lambda DNA are pre-digested with restriction enzymes - endonucleases that recognize and cut double-stranded DNA within or near defined base sequences. Digests are separated by agarose gel
Product Features: Cast iron hotplate Variable heat settings Overheat protection Corrosion resistant Power indicator Easy clean finish Non-slip rubber feet Hotplate diameter: 185mm Powe
These unstirred water baths are ideal for general laboratory use and are economical, reliable and very cost effective. Comprising of a high quality corrosion resistant seamless stainless steel tank, with a bright clean finish housed in a durable p
The DuoSource™ is our most popular electrophoresis power supply and runs gels quickly - in only 20-30 minutes at 150 V! Features: • Max Voltage: 150 Volts • Voltage Steps: 75 or 150 Volts • Max Curren
The successor to the bestselling EdvoCycler™ has been redesigned with improved PCR technology to be the best value among classroom thermal cyclers. The EdvoCycler™ 2 doubles the capacity of the origin
In this experiment, students will explore the biological process of bacterial transformation using E. coli and plasmid DNA. At the end of the activity, students will have experience observing and anal
In this experiment, your students will develop an understanding of bacterial transformation by plasmid DNA by introducing an opportunity to observe an acquired phenotypic trait of the transformed bact
FlashBlue™ is a proprietary DNA stain that offers simple and rapid staining of agarose gels. FlashBlue™ is provided as a concentrated liquid stain that, when diluted, can be used for both rapid and ov
This 50-fold concentrated Tris-Acetate EDTA buffer (TAE), pH 7.8-8.0, has been optimized for agarose gel electrophoresis of nucleic acids. One volume of buffer is added to every 49 volumes of distille
A cost affective way to introduce DNA electrophoresis to the classroom. The set provides all the equipment you need to run any DNA or dye electrophoresis kits with your students. Kit includes 1 x Hexa
Teach your students about restriction enzyme digests in the context of forensic science! Your students will cut DNA with restriction enzymes and then compare the banding pattern of the crime scene DNA
Give your students the opportunity to carry out PCR in the classroom! This kit provides easy to follow instructions for your students to develop various crime scene scenarios independently. Plasmid DN
This simple lab demonstrates detection of the mutation that causes Sickle Cell Anemia. In this simulation, your students will use electrophoresis to separate dyes that represent patient samples and co
Demonstrate how electrophoresis separates molecules on the basis of size and charge. A safe, colorful, fast and simple way to teach a technique that will engage your students. • Explore how gel electr
DNA obtained from a single hair left behind at a crime scene can be used to identify a criminal. In this experiment, your students will compare simulated crime scene DNA with that of two suspects. • L
Your class will make the invisible, visible! With this kit, your students will sample water and air and then grow any microbes present overnight. A safe and simple way to teach pollution. Group Size:
Investigate how agarose gel electrophoresis unlocks the color code used by food scientists to make colorful candies. Students will extract color activities from common candies and separate the dyes on
Your students can construct DNA models and then extract DNA from onions, strawberries or bananas. You provide the fruit or vegetables and 95-100% isopropyl alcohol, your students extract DNA. • Learn
After a crime has been committed, the evidence left behind can identify a potential culprit, although a single piece of evidence is not usually enough to convict someone. Even in this age of DNA, fing
The principles of diffusion and osmosis are applied to the movement of water within plants. Emphasis is given to water potential transport and the effect of the plant environment on transpiration. Gro
In this experiment, students will explore the biological process of bacterial transformation using E. coli and plasmid DNA. At the end of the activity, students will have experience observing and anal
Analysis of Eco RI Cleavage Patterns of Lambda DNA This experiment introduces the use of restriction enzymes as a tool to digest DNA at specific nucleotide sequences. Bateriophage lambda DNA has a lin
In this experiment, students will learn how to measure the rate of photosynthesis indirectly by studying the floating leaf disk assay, and test different variables that might affect the photosynthesis
ABOUT THIS PRODUCT: 1 EdvoCycler™ 2 (48 x 0.2 ml) 6 M12 Complete™ Package (14 x 7 cm Tray & 7 x 7 cm Trays (2) 3 QuadraSource™ Power Supply (10-300V, for 1 to 4 units) 6 Variable MicroPipette (5 - 50
This LabStation™ includes the following: 1 EdvoCycler™ Jr. (16 x 0.2 ml) 2 M12 Complete™ Package (14 x 7 cm Tray & 7 x 7 cm Trays (2) 1 QuadraSource™ Power Supply (10-300V, for 1 to 4 units) 2 Variabl
M12 Complete™ Electrophoresis Pac DuoSource™ 150 Power Supply (75 V or 150 V for 1 or 2 units) Fixed Volume MiniPipette (35 µl) Yellow Micropipet Tips(1 - 200 µl /2 Racks of 96) Whose DNA Was Left Beh
Protein InstaStain® sheets stain gels faster than conventional methods. Protein InstaStain® gives high quality and uniform gel staining with excellent results for photography. They are also environmen
Are you planning a virtual curriculum or looking for experiments ideal for distance learning? With MyLab™ custom kits from Edvotek, you can plan your curriculum and have all the materials sent directl
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
Showing products per page